geneid | 11227 |
---|---|
ensemblid | ENSG00000136542.9 |
hgncid | 4127 |
symbol | GALNT5 |
name | polypeptide N-acetylgalactosaminyltransferase 5 |
refseq_nuc | NM_014568.3 |
refseq_prot | NP_055383.1 |
ensembl_nuc | ENST00000259056.5 |
ensembl_prot | ENSP00000259056.4 |
mane_status | MANE Select |
chr | chr2 |
start | 157257705 |
end | 157318491 |
strand | + |
ver | v1.2 |
region | chr2:157257705-157318491 |
region5000 | chr2:157252705-157323491 |
regionname0 | GALNT5_chr2_157257705_157318491 |
regionname5000 | GALNT5_chr2_157252705_157323491 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 940 | 205 | 40 | 47 | 89 | 5 | 22 | 65 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002 | 0/0 | 940 | 33 | 28 | 3 | 0 | 0 | 2 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003 | 0/0 | 940 | 25 | 0 | 0 | 25 | 0 | 0 | 21 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004 | 0/0 | 940 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0005 | 0/0 | 940 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0006 | 0/0 | 940 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0007 | 0/0 | 940 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0008 | 0/0 | 940 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2823 | 164 | 21 | 39 | 79 | 5 | 19 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0002 | 1/0 | 2823 | 38 | 16 | 8 | 10 | 0 | 3 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0003 | 0/0 | 2823 | 20 | 15 | 3 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0004 | 0/0 | 2823 | 17 | 0 | 0 | 17 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0005 | 0/0 | 2823 | 13 | 13 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0006 | 0/0 | 2823 | 8 | 8 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0007 | 0/0 | 2823 | 8 | 0 | 0 | 8 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0008 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0009 | 0/0 | 2823 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0010 | 0/0 | 2823 | 3 | 1 | 1 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0011 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0012 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
c0013 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 7522 | 75 | 3 | 12 | 47 | 1 | 10 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0002 | 0/0 | 7522 | 39 | 2 | 11 | 22 | 2 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0003 | 0/0 | 7521 | 15 | 1 | 10 | 4 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0004 | 0/0 | 7522 | 9 | 4 | 0 | 1 | 0 | 4 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0005 | 0/0 | 7524 | 7 | 1 | 0 | 4 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0006 | 0/0 | 7524 | 5 | 0 | 1 | 1 | 1 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0007 | 0/0 | 7523 | 4 | 1 | 0 | 2 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0008 | 0/0 | 7522 | 4 | 0 | 4 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0009 | 0/0 | 7522 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0010 | 0/0 | 7531 | 4 | 3 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0011 | 0/0 | 7524 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0012 | 0/0 | 7523 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0013 | 0/0 | 7531 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0014 | 0/0 | 7529 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0015 | 0/0 | 7507 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0016 | 0/0 | 7522 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0017 | 0/0 | 7522 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0018 | 0/0 | 7520 | 2 | 1 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0019 | 0/0 | 7520 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0020 | 0/0 | 7523 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0021 | 0/0 | 7522 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0022 | 0/0 | 7522 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0023 | 0/0 | 7524 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0024 | 0/0 | 7522 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0025 | 0/0 | 7521 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0026 | 0/0 | 7522 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0027 | 0/0 | 7517 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0028 | 0/0 | 7521 | 2 | 1 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0029 | 0/0 | 7521 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0030 | 0/0 | 7522 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0031 | 0/0 | 7531 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0032 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0033 | 0/0 | 7520 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0034 | 0/0 | 7522 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0035 | 0/0 | 7523 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0036 | 0/0 | 7524 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0037 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0038 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0039 | 0/0 | 7523 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0040 | 0/0 | 7521 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0041 | 0/0 | 7519 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0042 | 0/0 | 7520 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0043 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0044 | 0/0 | 7520 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0045 | 0/0 | 7521 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0046 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0047 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0048 | 0/0 | 7521 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0049 | 0/0 | 7522 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0050 | 0/0 | 7523 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0051 | 0/0 | 7523 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0052 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0053 | 0/0 | 7522 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0054 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0055 | 0/0 | 7549 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0056 | 0/0 | 7548 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0057 | 0/0 | 7518 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0058 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0059 | 0/0 | 7524 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0060 | 0/0 | 7522 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0061 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0062 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0063 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0064 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0065 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0066 | 0/0 | 7519 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0067 | 0/0 | 7520 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0068 | 0/0 | 7523 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0069 | 0/0 | 7521 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0070 | 0/0 | 7521 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0071 | 0/0 | 7519 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0072 | 0/0 | 7520 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0073 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0074 | 0/0 | 7522 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0075 | 0/0 | 7521 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0076 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0077 | 0/0 | 7531 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0078 | 0/0 | 7527 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0079 | 0/0 | 7530 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0080 | 0/0 | 7531 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0081 | 0/0 | 7535 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0082 | 0/0 | 7533 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0083 | 0/0 | 7530 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0084 | 0/0 | 7531 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0085 | 0/0 | 7531 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0086 | 0/0 | 7531 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0087 | 0/0 | 7531 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0088 | 0/0 | 7526 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0089 | 0/0 | 7528 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0090 | 0/0 | 7530 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0091 | 0/0 | 7531 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0092 | 0/0 | 7532 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0093 | 0/0 | 7537 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0094 | 0/0 | 7534 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0095 | 0/0 | 7541 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0096 | 0/0 | 7537 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0097 | 0/0 | 7532 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0098 | 0/0 | 7535 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0099 | 0/0 | 7540 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0100 | 0/0 | 7522 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
t0101 | 0/0 | 7525 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2823 | 164 | 21 | 39 | 79 | 5 | 19 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002 | 1/0 | 2823 | 38 | 16 | 8 | 10 | 0 | 3 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0009 | 0/0 | 2823 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003 | 0/0 | 2823 | 20 | 15 | 3 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005 | 0/0 | 2823 | 13 | 13 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004 | 0/0 | 2823 | 17 | 0 | 0 | 17 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0007 | 0/0 | 2823 | 8 | 0 | 0 | 8 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0006 | 0/0 | 2823 | 8 | 8 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0011 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0005c0008 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0006c0010 | 0/0 | 2823 | 3 | 1 | 1 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0007c0012 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0008c0013 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10344 | 58 | 3 | 12 | 33 | 1 | 8 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0002 | 0/0 | 10344 | 24 | 0 | 6 | 14 | 2 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0003 | 0/0 | 10343 | 12 | 0 | 10 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0004 | 0/0 | 10344 | 6 | 1 | 0 | 1 | 0 | 4 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0005 | 0/0 | 10346 | 5 | 1 | 0 | 2 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0006 | 0/0 | 10346 | 3 | 0 | 1 | 1 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0007 | 0/0 | 10345 | 3 | 0 | 0 | 2 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0008 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0009 | 0/0 | 10344 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0010 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0011 | 0/0 | 10346 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0015 | 0/0 | 10329 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0016 | 0/0 | 10344 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0020 | 0/0 | 10345 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0021 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0022 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0024 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0028 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0029 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0030 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0033 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0035 | 0/0 | 10345 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0036 | 0/0 | 10346 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0037 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0038 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0039 | 0/0 | 10345 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0040 | 0/0 | 10343 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0046 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0048 | 0/0 | 10343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0049 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0050 | 0/0 | 10345 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0052 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0053 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0054 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0055 | 0/0 | 10371 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0056 | 0/0 | 10370 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0057 | 0/0 | 10340 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0058 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0059 | 0/0 | 10346 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0060 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0062 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0069 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0070 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0073 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0075 | 0/0 | 10343 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0080 | 0/0 | 10353 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0081 | 0/0 | 10357 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0082 | 0/0 | 10355 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0088 | 0/0 | 10348 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0093 | 0/0 | 10359 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0094 | 0/0 | 10356 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0095 | 0/0 | 10363 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0001t0097 | 0/0 | 10354 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0001 | 1/0 | 10344 | 6 | 0 | 0 | 3 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0002 | 0/0 | 10344 | 8 | 0 | 5 | 3 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0003 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0008 | 0/0 | 10344 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0010 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0014 | 0/0 | 10351 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0021 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0029 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0030 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0031 | 0/0 | 10353 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0034 | 0/0 | 10344 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0047 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0051 | 0/0 | 10345 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0066 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0076 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0077 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0078 | 0/0 | 10349 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0086 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0087 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0091 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0092 | 0/0 | 10354 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0096 | 0/0 | 10359 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0098 | 0/0 | 10357 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0002t0099 | 0/0 | 10362 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0009t0025 | 0/0 | 10343 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0001c0009t0071 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0004 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0006 | 0/0 | 10346 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0007 | 0/0 | 10345 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0008 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0017 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0023 | 0/0 | 10346 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0024 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0026 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0028 | 0/0 | 10343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0041 | 0/0 | 10341 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0042 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0061 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0065 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0067 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0072 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0100 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0003t0101 | 0/0 | 10347 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0002 | 0/0 | 10344 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0003 | 0/0 | 10343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0012 | 0/0 | 10345 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0017 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0019 | 0/0 | 10342 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0027 | 0/0 | 10339 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0044 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0002c0005t0064 | 0/0 | 10340 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0001 | 0/0 | 10344 | 9 | 0 | 0 | 9 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0002 | 0/0 | 10344 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0005 | 0/0 | 10346 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0018 | 0/0 | 10342 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0043 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0068 | 0/0 | 10345 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0004t0074 | 0/0 | 10344 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0007t0001 | 0/0 | 10344 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0007t0002 | 0/0 | 10344 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0007t0003 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0007t0011 | 0/0 | 10346 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0003c0007t0045 | 0/0 | 10343 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0006t0010 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0006t0013 | 0/0 | 10353 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0006t0014 | 0/0 | 10351 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0006t0085 | 0/0 | 10353 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0006t0090 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0011t0079 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0004c0011t0089 | 0/0 | 10350 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0005c0008t0004 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0005c0008t0018 | 0/0 | 10342 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0005c0008t0026 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0005c0008t0063 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0006c0010t0010 | 0/0 | 10353 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0006c0010t0083 | 0/0 | 10352 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0006c0010t0084 | 0/0 | 10353 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0007c0012t0022 | 0/0 | 10344 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
a0008c0013t0032 | 0/0 | 10344 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | copy fasta | chr2 | 157252705 | 157323491 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0009g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0015g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0016g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0016g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0020g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0021g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0022g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0028g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0029g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0030g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0033g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0035g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0036g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0037g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0038g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0039g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0040g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0046g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0048g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0049g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0050g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0052g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0053g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0054g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0055g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0056g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0057g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0058g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0059g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0060g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0062g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0069g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0070g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0073g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0075g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0080g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0081g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0082g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0088g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0093g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0094g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0095g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0001t0097g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0014g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0029g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0030g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0031g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0034g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0047g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0051g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0066g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0076g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0077g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0078g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0086g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0087g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0091g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0092g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0096g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0098g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0002t0099g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0009t0025g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0009t0025g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0001c0009t0071g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0023g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0023g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0024g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0026g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0028g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0041g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0042g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0061g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0065g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0067g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0072g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0100g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0003t0101g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0012g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0017g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0019g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0019g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0027g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0027g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0044g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0002c0005t0064g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0018g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0043g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0068g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0004t0074g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0003c0007t0045g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0085g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0006t0090g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0011t0079g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0004c0011t0089g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0026g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0005c0008t0063g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0006c0010t0010g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0006c0010t0083g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0006c0010t0084g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0007c0012t0022g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
a0008c0013t0032g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0048 | EUR | GBR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | FIN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0005 | EUR | FIN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00438 | hp1 | a0001 | c0001 | t0021 | g0038 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00438 | hp2 | a0001 | c0001 | t0050 | g0149 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0147 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00597 | hp2 | a0003 | c0004 | t0001 | g0231 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00609 | hp2 | a0001 | c0001 | t0030 | g0035 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00639 | hp1 | a0002 | c0003 | t0023 | g0188 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00673 | hp1 | a0003 | c0004 | t0005 | g0223 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00673 | hp2 | a0001 | c0001 | t0055 | g0012 | EAS | CHS | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00735 | hp2 | a0002 | c0003 | t0008 | g0190 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG00741 | hp2 | a0001 | c0002 | t0051 | g0143 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01071 | hp2 | a0001 | c0001 | t0022 | g0115 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01074 | hp2 | a0001 | c0001 | t0080 | g0237 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0056 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01109 | hp2 | a0001 | c0001 | t0053 | g0010 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01168 | hp1 | a0001 | c0001 | t0075 | g0074 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01243 | hp1 | a0006 | c0010 | t0084 | g0210 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01243 | hp2 | a0001 | c0001 | t0049 | g0159 | AMR | PUR | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01256 | hp1 | a0001 | c0001 | t0036 | g0004 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01258 | hp1 | a0001 | c0001 | t0035 | g0004 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01261 | hp1 | a0001 | c0001 | t0057 | g0005 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01261 | hp2 | a0002 | c0003 | t0024 | g0208 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01433 | hp1 | a0001 | c0001 | t0060 | g0076 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01884 | hp1 | a0004 | c0006 | t0090 | g0185 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01891 | hp1 | a0002 | c0005 | t0002 | g0205 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01891 | hp2 | a0004 | c0011 | t0079 | g0176 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01952 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01981 | hp2 | a0001 | c0002 | t0008 | g0089 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02040 | hp1 | a0001 | c0001 | t0011 | g0130 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02040 | hp2 | a0001 | c0001 | t0029 | g0061 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02055 | hp1 | a0002 | c0003 | t0067 | g0165 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02055 | hp2 | a0002 | c0003 | t0026 | g0166 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02071 | hp1 | a0003 | c0004 | t0005 | g0228 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02074 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02083 | hp1 | a0003 | c0007 | t0001 | g0232 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | CDX | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02257 | hp1 | a0002 | c0005 | t0027 | g0207 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02257 | hp2 | a0001 | c0001 | t0062 | g0108 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02258 | hp1 | a0001 | c0002 | t0010 | g0252 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02258 | hp2 | a0002 | c0005 | t0012 | g0013 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02293 | hp2 | a0001 | c0002 | t0008 | g0088 | AMR | PEL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02572 | hp1 | a0001 | c0002 | t0092 | g0245 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02572 | hp2 | a0001 | c0002 | t0014 | g0258 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02602 | hp1 | a0001 | c0002 | t0034 | g0093 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02615 | hp1 | a0001 | c0001 | t0073 | g0087 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02615 | hp2 | a0002 | c0005 | t0017 | g0206 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02622 | hp1 | a0001 | c0001 | t0015 | g0249 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02622 | hp2 | a0002 | c0005 | t0027 | g0202 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02630 | hp1 | a0005 | c0008 | t0026 | g0172 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02630 | hp2 | a0002 | c0005 | t0012 | g0187 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02647 | hp1 | a0004 | c0006 | t0013 | g0182 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02647 | hp2 | a0005 | c0008 | t0063 | g0171 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02683 | hp2 | a0001 | c0001 | t0016 | g0154 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02698 | hp2 | a0002 | c0003 | t0006 | g0174 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02717 | hp1 | a0005 | c0008 | t0004 | g0201 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02717 | hp2 | a0002 | c0003 | t0100 | g0197 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02723 | hp1 | a0004 | c0006 | t0014 | g0183 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02723 | hp2 | a0001 | c0002 | t0076 | g0251 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02809 | hp1 | a0005 | c0008 | t0018 | g0170 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0255 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02886 | hp1 | a0002 | c0005 | t0044 | g0169 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02886 | hp2 | a0001 | c0001 | t0082 | g0260 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02895 | hp1 | a0001 | c0002 | t0091 | g0240 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02895 | hp2 | a0001 | c0002 | t0031 | g0015 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02896 | hp1 | a0001 | c0009 | t0025 | g0134 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02896 | hp2 | a0002 | c0003 | t0028 | g0163 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02897 | hp1 | a0001 | c0002 | t0031 | g0015 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02897 | hp2 | a0002 | c0003 | t0004 | g0164 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02965 | hp1 | a0001 | c0001 | t0048 | g0070 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02965 | hp2 | a0001 | c0002 | t0099 | g0257 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02970 | hp1 | a0001 | c0002 | t0098 | g0244 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0254 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02976 | hp1 | a0002 | c0005 | t0064 | g0203 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02976 | hp2 | a0001 | c0009 | t0071 | g0009 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03017 | hp2 | a0001 | c0001 | t0016 | g0113 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03130 | hp1 | a0001 | c0002 | t0077 | g0250 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03130 | hp2 | a0001 | c0002 | t0078 | g0247 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03139 | hp1 | a0004 | c0011 | t0089 | g0177 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03139 | hp2 | a0002 | c0005 | t0012 | g0013 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03195 | hp2 | a0002 | c0003 | t0041 | g0195 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03209 | hp1 | a0001 | c0002 | t0066 | g0096 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03209 | hp2 | a0004 | c0006 | t0013 | g0179 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03225 | hp1 | a0002 | c0003 | t0023 | g0191 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03225 | hp2 | a0001 | c0001 | t0097 | g0242 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03239 | hp1 | a0001 | c0001 | t0040 | g0081 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03453 | hp1 | a0002 | c0005 | t0003 | g0204 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03453 | hp2 | a0006 | c0010 | t0083 | g0184 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03486 | hp1 | a0002 | c0003 | t0061 | g0194 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03490 | hp1 | a0002 | c0003 | t0006 | g0173 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03516 | hp1 | a0002 | c0005 | t0002 | g0198 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03516 | hp2 | a0002 | c0003 | t0004 | g0192 | AFR | ESN | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03540 | hp1 | a0001 | c0001 | t0093 | g0243 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03579 | hp2 | a0004 | c0006 | t0010 | g0178 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0054 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0126 | SAS | BEB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | STU | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18522 | hp1 | a0001 | c0002 | t0086 | g0248 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18522 | hp2 | a0002 | c0005 | t0019 | g0199 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18747 | hp2 | a0001 | c0002 | t0021 | g0051 | EAS | CHB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18906 | hp1 | a0001 | c0002 | t0047 | g0092 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18906 | hp2 | a0001 | c0001 | t0088 | g0246 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18946 | hp1 | a0003 | c0004 | t0001 | g0221 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18959 | hp1 | a0001 | c0001 | t0070 | g0117 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18960 | hp2 | a0001 | c0002 | t0029 | g0156 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18961 | hp1 | a0003 | c0007 | t0045 | g0211 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18961 | hp2 | a0003 | c0007 | t0011 | g0233 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18963 | hp2 | a0003 | c0004 | t0001 | g0213 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18964 | hp1 | a0003 | c0004 | t0002 | g0214 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18964 | hp2 | a0001 | c0001 | t0028 | g0150 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18965 | hp1 | a0003 | c0007 | t0002 | g0234 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18965 | hp2 | a0001 | c0001 | t0052 | g0022 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18968 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18968 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18970 | hp1 | a0001 | c0002 | t0030 | g0032 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18971 | hp2 | a0001 | c0001 | t0039 | g0122 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18973 | hp1 | a0003 | c0004 | t0001 | g0224 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18977 | hp1 | a0001 | c0001 | t0020 | g0027 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18979 | hp2 | a0003 | c0007 | t0002 | g0217 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18981 | hp2 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18982 | hp1 | a0003 | c0004 | t0068 | g0218 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18985 | hp2 | a0001 | c0001 | t0038 | g0079 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18990 | hp2 | a0001 | c0001 | t0037 | g0132 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18991 | hp1 | a0001 | c0001 | t0054 | g0021 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18991 | hp2 | a0003 | c0004 | t0001 | g0216 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18992 | hp2 | a0003 | c0007 | t0003 | g0225 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18999 | hp1 | a0001 | c0001 | t0009 | g0008 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA18999 | hp2 | a0001 | c0001 | t0056 | g0124 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19002 | hp1 | a0001 | c0001 | t0058 | g0023 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19002 | hp2 | a0003 | c0004 | t0001 | g0230 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19003 | hp1 | a0003 | c0004 | t0001 | g0229 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19011 | hp2 | a0003 | c0004 | t0043 | g0226 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19030 | hp1 | a0001 | c0002 | t0096 | g0239 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19030 | hp2 | a0002 | c0003 | t0072 | g0167 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19043 | hp1 | a0004 | c0006 | t0014 | g0168 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19043 | hp2 | a0002 | c0003 | t0042 | g0189 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19058 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19062 | hp1 | a0001 | c0001 | t0069 | g0094 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19064 | hp2 | a0001 | c0001 | t0059 | g0049 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19065 | hp2 | a0003 | c0004 | t0018 | g0219 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19068 | hp2 | a0003 | c0007 | t0001 | g0222 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19074 | hp1 | a0003 | c0007 | t0002 | g0212 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19076 | hp2 | a0001 | c0001 | t0009 | g0151 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19084 | hp1 | a0001 | c0001 | t0020 | g0007 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19085 | hp1 | a0001 | c0001 | t0011 | g0109 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19088 | hp1 | a0003 | c0004 | t0074 | g0220 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19088 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19091 | hp2 | a0003 | c0004 | t0002 | g0227 | EAS | JPT | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19240 | hp1 | a0004 | c0006 | t0085 | g0181 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA19240 | hp2 | a0001 | c0009 | t0025 | g0009 | AFR | YRI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20129 | hp1 | a0002 | c0003 | t0101 | g0196 | AFR | ASW | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20129 | hp2 | a0004 | c0006 | t0013 | g0180 | AFR | ASW | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20752 | hp2 | a0006 | c0010 | t0010 | g0175 | EUR | TSI | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG01123 | hp2 | a0007 | c0012 | t0022 | g0137 | AMR | CLM | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02109 | hp1 | a0008 | c0013 | t0032 | g0261 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02109 | hp2 | a0002 | c0003 | t0017 | g0193 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02486 | hp1 | a0001 | c0001 | t0024 | g0060 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02486 | hp2 | a0002 | c0005 | t0019 | g0200 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02559 | hp1 | a0002 | c0003 | t0007 | g0209 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG02559 | hp2 | a0002 | c0003 | t0065 | g0186 | AFR | ACB | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03471 | hp1 | a0001 | c0002 | t0087 | g0259 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
HG03471 | hp2 | a0001 | c0001 | t0095 | g0238 | AFR | MSL | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20300 | hp1 | a0001 | c0001 | t0033 | g0256 | AFR | USA | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA20300 | hp2 | a0001 | c0001 | t0046 | g0106 | AFR | USA | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA21309 | hp1 | a0001 | c0001 | t0081 | g0241 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
NA21309 | hp2 | a0001 | c0001 | t0094 | g0253 | AFR | LWK | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0146 | REF | REF | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0090 | REF | REF | GALNT5_chr2_157252705_157323491 | GALNT5 | chr2 | 157252705 | 157323491 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157258312
|
C | T | 1 | a0003 | 25 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(22): Show |
missense_variant | MODERATE | c.230C>T | p.Pro77Leu | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 608/10344 | 230/2823 | 77/940 | chr2 | 157258312 | ||
chr2:157258518
|
G | A | 1 | a0005 | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
missense_variant | MODERATE | c.436G>A | p.Gly146Arg | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 814/10344 | 436/2823 | 146/940 | chr2 | 157258518 | ||
chr2:157258540
|
C | T | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.458C>T | p.Ala153Val | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 836/10344 | 458/2823 | 153/940 | chr2 | 157258540 | ||
chr2:157258617
|
A | T | 2 | a0004a0006 | 13 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
missense_variant | MODERATE | c.535A>T | p.Thr179Ser | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 913/10344 | 535/2823 | 179/940 | chr2 | 157258617 | ||
chr2:157284294
|
G | C | 3 | a0002a0004a0005 | 47 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(44): Show |
missense_variant | MODERATE | c.1467G>C | p.Gln489His | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/10 | 1845/10344 | 1467/2823 | 489/940 | chr2 | 157284294 | ||
chr2:157296405
|
T | C | 1 | a0007 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.1889T>C | p.Val630Ala | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/10 | 2267/10344 | 1889/2823 | 630/940 | chr2 | 157296405 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157258247
|
A | C | 1 | a0008c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.165A>C | p.Ile55Ile | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 543/10344 | 165/2823 | 55/940 | chr2 | 157258247 | ||
chr2:157258517
|
C | T | 1 | a0008c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.435C>T | p.Asp145Asp | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 813/10344 | 435/2823 | 145/940 | chr2 | 157258517 | ||
chr2:157258535
|
T | C | 1 | a0008c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.453T>C | p.Pro151Pro | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 831/10344 | 453/2823 | 151/940 | chr2 | 157258535 | ||
chr2:157300849
|
C | T | 9 | a0001c0001a0001c0009a0002c0003others(6): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
synonymous_variant | LOW | c.2289C>T | p.His763His | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/10 | 2667/10344 | 2289/2823 | 763/940 | chr2 | 157300849 | ||
chr2:157300948
|
G | A | 1 | a0001c0009 | 3 | HG02896.hp1 HG02976.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2388G>A | p.Leu796Leu | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/10 | 2766/10344 | 2388/2823 | 796/940 | chr2 | 157300948 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157257756
|
C | T | 2 | a0002c0003t0100a0002c0003t0101 | 2 | HG02717.hp2 NA20129.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-327C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | chr2 | 157257756 | ||||||
chr2:157257836
|
T | C | 1 | a0008c0013t0032 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-247T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 247 | chr2 | 157257836 | |||||
chr2:157257986
|
T | TCTG | 1 | a0002c0005t0012 | 3 | HG02258.hp2 HG02630.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73_-71dupGCT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | ||||
chr2:157257986
|
T | TCTGCTGC others(2): Show |
23 | a0001c0001t0010a0001c0001t0080a0001c0001t0081others(20): Show | 27 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-79_-71dupGCTGCTGC others(1): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | ||||
chr2:157257986
|
T | TCTGCTGC others(5): Show |
2 | a0001c0002t0091a0001c0002t0092 | 2 | HG02572.hp1 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-82_-71dupGCTGCTGC others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | ||||
chr2:157257986
|
T | TCTGCTGC others(8): Show |
6 | a0001c0001t0093a0001c0001t0094a0001c0001t0095others(3): Show | 6 | HG02970.hp1 HG03225.hp2 HG03471.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-71dupGCTGCTGC others(7): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | ||||
chr2:157257986
|
T | TCTGCTGC others(11): Show |
1 | a0001c0002t0099 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88_-71dupGCTGCTGC others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 70 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | ||||
chr2:157257986
|
TCTGCTG | T | 2 | a0001c0001t0015a0001c0001t0033 | 3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-76_-71delGCTGCT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/10 | 71 | INFO_REALIGN_3_PRIME | chr2 | 157257986 | ||||
chr2:157311472
|
T | A | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*124T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 124 | chr2 | 157311472 | |||||
chr2:157311530
|
T | C | 2 | a0001c0001t0016a0001c0002t0034 | 3 | HG02602.hp1 HG02683.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*182T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 182 | chr2 | 157311530 | |||||
chr2:157311588
|
A | G | 4 | a0001c0001t0029a0001c0001t0030a0001c0002t0029others(1): Show | 4 | HG00609.hp2 HG02040.hp2 NA18960.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*240A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 240 | chr2 | 157311588 | |||||
chr2:157311834
|
C | T | 1 | a0001c0001t0075 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 486 | chr2 | 157311834 | |||||
chr2:157311837
|
T | C | 2 | a0001c0001t0035a0001c0001t0036 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*489T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 489 | chr2 | 157311837 | |||||
chr2:157311908
|
C | T | 1 | a0003c0004t0074 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*560C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 560 | chr2 | 157311908 | |||||
chr2:157311986
|
G | A | 1 | a0001c0001t0037 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 638 | chr2 | 157311986 | |||||
chr2:157312033
|
C | T | 1 | a0001c0001t0073 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 685 | chr2 | 157312033 | |||||
chr2:157312169
|
G | A | 1 | a0001c0001t0038 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 821 | chr2 | 157312169 | |||||
chr2:157312228
|
A | G | 1 | a0008c0013t0032 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 880 | chr2 | 157312228 | |||||
chr2:157312328
|
G | A | 1 | a0001c0001t0093 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 980 | chr2 | 157312328 | |||||
chr2:157312682
|
C | T | 1 | a0002c0003t0072 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1334 | chr2 | 157312682 | |||||
chr2:157312716
|
A | G | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1368 | chr2 | 157312716 | |||||
chr2:157312753
|
A | T | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1405A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1405 | chr2 | 157312753 | |||||
chr2:157312815
|
A | G | 1 | a0001c0002t0034 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1467 | chr2 | 157312815 | |||||
chr2:157312875
|
T | C | 1 | a0001c0001t0039 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1527T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1527 | chr2 | 157312875 | |||||
chr2:157312987
|
A | G | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1639A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1639 | chr2 | 157312987 | |||||
chr2:157313100
|
G | A | 22 | a0001c0001t0015a0001c0001t0029a0001c0001t0040others(19): Show | 27 | HG02040.hp2 HG02109.hp2 HG02258.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1752G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1752 | chr2 | 157313100 | |||||
chr2:157313154
|
C | T | 1 | a0001c0002t0099 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1806C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1806 | chr2 | 157313154 | |||||
chr2:157313275
|
T | G | 3 | a0001c0001t0029a0001c0001t0040a0001c0002t0029 | 3 | HG02040.hp2 HG03239.hp1 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1927T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1927 | chr2 | 157313275 | |||||
chr2:157313321
|
G | A | 3 | a0001c0001t0046a0001c0001t0048a0001c0002t0047 | 3 | HG02965.hp1 NA18906.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1973G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 1973 | chr2 | 157313321 | |||||
chr2:157313505
|
T | C | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2157T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2157 | chr2 | 157313505 | |||||
chr2:157313566
|
T | C | 1 | a0001c0001t0049 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2218T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2218 | chr2 | 157313566 | |||||
chr2:157314211
|
T | TA | 12 | a0001c0001t0020a0001c0001t0050a0001c0001t0073others(9): Show | 13 | HG00438.hp2 HG00741.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2880dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2881 | INFO_REALIGN_3_PRIME | chr2 | 157314211 | ||||
chr2:157314211
|
TA | T | 13 | a0001c0001t0028a0001c0001t0029a0001c0001t0040others(10): Show | 13 | HG01168.hp1 HG01884.hp1 HG02040.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2880delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 2880 | INFO_REALIGN_3_PRIME | chr2 | 157314211 | ||||
chr2:157314348
|
C | T | 5 | a0001c0002t0014a0001c0002t0098a0002c0003t0067others(2): Show | 6 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3000C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3000 | chr2 | 157314348 | |||||
chr2:157314404
|
G | A | 1 | a0001c0001t0080 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3056G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3056 | chr2 | 157314404 | |||||
chr2:157314586
|
T | C | 2 | a0001c0001t0021a0001c0002t0021 | 2 | HG00438.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3238T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3238 | chr2 | 157314586 | |||||
chr2:157314983
|
CAGG | C | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3638_*3640delGAG | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3638 | INFO_REALIGN_3_PRIME | chr2 | 157314983 | ||||
chr2:157315002
|
C | T | 1 | a0001c0001t0080 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3654C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3654 | chr2 | 157315002 | |||||
chr2:157315029
|
A | G | 42 | a0001c0001t0015a0001c0001t0024a0001c0001t0029others(39): Show | 47 | HG00639.hp1 HG01261.hp2 HG01891.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3681A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3681 | chr2 | 157315029 | |||||
chr2:157315081
|
AAAT | A | 9 | a0001c0001t0015a0001c0001t0073a0001c0002t0076others(6): Show | 10 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3746_*3748delAAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3746 | INFO_REALIGN_3_PRIME | chr2 | 157315081 | ||||
chr2:157315083
|
A | T | 1 | a0001c0001t0062 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3735A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 3735 | chr2 | 157315083 | |||||
chr2:157315440
|
A | T | 2 | a0001c0001t0015a0001c0002t0076 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4092A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 4092 | chr2 | 157315440 | |||||
chr2:157315456
|
A | C | 1 | a0002c0003t0061 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4108A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 4108 | chr2 | 157315456 | |||||
chr2:157316235
|
A | G | 3 | a0001c0001t0022a0001c0001t0060a0007c0012t0022 | 3 | HG01071.hp2 HG01123.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4887A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 4887 | chr2 | 157316235 | |||||
chr2:157316619
|
A | G | 1 | a0001c0002t0031 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5271A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5271 | chr2 | 157316619 | |||||
chr2:157316638
|
T | C | 2 | a0001c0001t0073a0001c0002t0078 | 2 | HG02615.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5290T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5290 | chr2 | 157316638 | |||||
chr2:157316697
|
T | C | 1 | a0001c0001t0052 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5349 | chr2 | 157316697 | |||||
chr2:157316735
|
G | A | 1 | a0001c0001t0053 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5387G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5387 | chr2 | 157316735 | |||||
chr2:157316946
|
A | G | 2 | a0001c0001t0009a0001c0001t0059 | 5 | HG00544.hp2 NA18999.hp1 NA19064.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5598A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5598 | chr2 | 157316946 | |||||
chr2:157317109
|
A | C | 3 | a0002c0005t0012a0002c0005t0019a0002c0005t0044 | 6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5761A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5761 | chr2 | 157317109 | |||||
chr2:157317174
|
G | GTA | 7 | a0001c0001t0005a0001c0001t0006a0001c0001t0059others(4): Show | 16 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5850_*5851dupAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5852 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | ||||
chr2:157317174
|
G | GTATA | 3 | a0001c0001t0033a0001c0001t0081a0001c0001t0095 | 3 | HG03471.hp2 NA20300.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5848_*5851dupATAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5852 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | ||||
chr2:157317174
|
GTA | G | 10 | a0001c0001t0073a0001c0002t0014a0001c0002t0078others(7): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5850_*5851delAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5850 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | ||||
chr2:157317174
|
GTATA | G | 3 | a0001c0001t0057a0002c0003t0065a0002c0005t0064 | 3 | HG01261.hp1 HG02559.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5848_*5851delATAT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5848 | INFO_REALIGN_3_PRIME | chr2 | 157317174 | ||||
chr2:157317176
|
A | G | 1 | a0001c0001t0058 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5828A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5828 | chr2 | 157317176 | |||||
chr2:157317191
|
TATA | T | 6 | a0001c0001t0015a0001c0001t0094a0001c0002t0066others(3): Show | 7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5844_*5846delATA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5844 | chr2 | 157317191 | |||||
chr2:157317191
|
TATATA | T | 3 | a0001c0001t0088a0001c0001t0097a0002c0005t0027 | 4 | HG02257.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5844_*5848delATAT others(1): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5844 | chr2 | 157317191 | |||||
chr2:157317194
|
A | T | 2 | a0001c0002t0092a0004c0006t0085 | 2 | HG02572.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5846A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5846 | chr2 | 157317194 | |||||
chr2:157317196
|
A | T | 21 | a0001c0001t0008a0001c0001t0015a0001c0001t0052others(18): Show | 24 | HG00735.hp2 HG01891.hp2 HG01952.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5848A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5848 | chr2 | 157317196 | |||||
chr2:157317197
|
TA | T | 7 | a0001c0001t0003a0001c0002t0003a0001c0009t0025others(4): Show | 19 | HG01106.hp1 HG01361.hp1 HG01361.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5850delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5850 | chr2 | 157317197 | |||||
chr2:157317198
|
A | AT | 5 | a0001c0001t0007a0001c0001t0035a0001c0001t0039others(2): Show | 7 | HG00280.hp2 HG00673.hp2 HG01258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5861dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5862 | INFO_REALIGN_3_PRIME | chr2 | 157317198 | ||||
chr2:157317198
|
A | ATT | 8 | a0001c0001t0011a0001c0001t0036a0001c0001t0082others(5): Show | 9 | HG01256.hp1 HG02040.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5860_*5861dupTT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5862 | INFO_REALIGN_3_PRIME | chr2 | 157317198 | ||||
chr2:157317198
|
A | T | 44 | a0001c0001t0002a0001c0001t0008a0001c0001t0015others(41): Show | 82 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*5850A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5850 | chr2 | 157317198 | |||||
chr2:157317198
|
ATT | A | 5 | a0002c0005t0012a0002c0005t0019a0002c0005t0044others(2): Show | 8 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5860_*5861delTT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5860 | INFO_REALIGN_3_PRIME | chr2 | 157317198 | ||||
chr2:157317200
|
T | A | 13 | a0001c0001t0004a0001c0001t0006a0001c0001t0028others(10): Show | 25 | HG00099.hp2 HG00438.hp2 HG01106.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5852T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5852 | chr2 | 157317200 | |||||
chr2:157317247
|
C | T | 1 | a0001c0001t0060 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5899C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5899 | chr2 | 157317247 | |||||
chr2:157317286
|
T | C | 5 | a0002c0003t0017a0002c0003t0041a0002c0003t0042others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5938T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 5938 | chr2 | 157317286 | |||||
chr2:157317362
|
T | C | 1 | a0001c0001t0058 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6014T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6014 | chr2 | 157317362 | |||||
chr2:157317382
|
T | G | 1 | a0001c0002t0087 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6034T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6034 | chr2 | 157317382 | |||||
chr2:157317414
|
T | G | 1 | a0001c0001t0054 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6066T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6066 | chr2 | 157317414 | |||||
chr2:157317960
|
C | G | 1 | a0001c0002t0031 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6612C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6612 | chr2 | 157317960 | |||||
chr2:157318122
|
A | T | 3 | a0001c0001t0024a0002c0003t0023a0002c0003t0024 | 4 | HG00639.hp1 HG01261.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6774A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6774 | chr2 | 157318122 | |||||
chr2:157318149
|
A | T | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG00673.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6801A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6801 | chr2 | 157318149 | |||||
chr2:157318154
|
T | TTATTTTT others(19): Show |
2 | a0001c0001t0055a0001c0001t0056 | 2 | HG00673.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6806_*6807insTATT others(22): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 10/10 | 6807 | chr2 | 157318154 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:157259616
|
C | T | 26 | a0001c0001t0010g0254a0001c0001t0015g0249a0001c0001t0015g0255others(23): Show | 27 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1454+80C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157259616 | ||||||
chr2:157259729
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1454+193T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157259729 | ||||||
chr2:157260183
|
A | G | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1454+647A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260183 | ||||||
chr2:157260260
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA18959.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1454+724A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260260 | ||||||
chr2:157260788
|
C | T | 74 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(71): Show | 76 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1454+1252C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260788 | ||||||
chr2:157260893
|
T | C | 74 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(71): Show | 76 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1454+1357T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260893 | ||||||
chr2:157260977
|
T | C | 1 | a0001c0001t0080g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1454+1441T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157260977 | ||||||
chr2:157261171
|
C | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0003g0018others(1): Show | 4 | HG00741.hp1 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+1635C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261171 | ||||||
chr2:157261242
|
G | T | 26 | a0001c0001t0001g0215a0001c0002t0003g0162a0003c0004t0001g0014others(23): Show | 27 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1454+1706G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261242 | ||||||
chr2:157261317
|
G | A | 8 | a0001c0001t0081g0241a0001c0001t0093g0243a0001c0001t0095g0238others(5): Show | 8 | HG02572.hp1 HG02895.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454+1781G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261317 | ||||||
chr2:157261357
|
C | T | 3 | a0003c0007t0001g0232a0003c0007t0002g0234a0003c0007t0011g0233 | 3 | HG02083.hp1 NA18961.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1454+1821C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261357 | ||||||
chr2:157261479
|
G | A | 1 | a0001c0001t0054g0021 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1454+1943G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261479 | ||||||
chr2:157261538
|
C | T | 13 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0155others(10): Show | 13 | HG00438.hp2 HG01243.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454+2002C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157261538 | ||||||
chr2:157262112
|
G | A | 74 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(71): Show | 76 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1454+2576G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262112 | ||||||
chr2:157262155
|
ACATAACT others(2): Show |
A | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+2624_1454+263 others(13): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262155 | |||||
chr2:157262207
|
T | TA | 60 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0026others(57): Show | 65 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1454+2689dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262207 | |||||
chr2:157262207
|
T | TAA | 6 | a0001c0001t0052g0022a0001c0001t0058g0023a0001c0002t0001g0024others(3): Show | 6 | NA18961.hp1 NA18963.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+2688_1454+268 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262207 | |||||
chr2:157262207
|
TA | T | 9 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0002t0031g0015others(6): Show | 10 | HG01358.hp1 HG01891.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454+2689delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262207 | |||||
chr2:157262225
|
A | T | 2 | a0002c0003t0007g0209a0002c0003t0024g0208 | 2 | HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1454+2689A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262225 | ||||||
chr2:157262287
|
G | A | 1 | a0001c0001t0006g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1454+2751G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262287 | ||||||
chr2:157262362
|
C | CA | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+2827dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262362 | |||||
chr2:157262454
|
T | C | 2 | a0001c0001t0010g0254a0001c0001t0094g0253 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1454+2918T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262454 | ||||||
chr2:157262484
|
AAAAATTA others(784): Show |
A | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+2953_1454+374 others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262484 | |||||
chr2:157262658
|
CAACAAT | C | 71 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(68): Show | 73 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1454+3125_1454+313 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262658 | |||||
chr2:157262661
|
CAAT | C | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3128_1454+313 others(7): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262661 | |||||
chr2:157262819
|
C | CT | 18 | a0001c0001t0001g0020a0001c0001t0001g0144a0001c0001t0001g0146others(15): Show | 19 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1454+3310dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262819 | |||||
chr2:157262819
|
CTTTTT | C | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0216others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+3306_1454+331 others(9): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262819 | |||||
chr2:157262819
|
CTTTTTT | C | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1454+3305_1454+331 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157262819 | |||||
chr2:157262897
|
G | A | 1 | a0001c0001t0059g0049 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1454+3361G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262897 | ||||||
chr2:157262921
|
G | C | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3385G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262921 | ||||||
chr2:157262972
|
C | A | 1 | a0002c0005t0027g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1454+3436C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262972 | ||||||
chr2:157262990
|
G | A | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3454G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157262990 | ||||||
chr2:157263027
|
C | A | 2 | a0001c0002t0014g0258a0001c0002t0087g0259 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1454+3491C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263027 | ||||||
chr2:157263046
|
C | T | 2 | a0001c0001t0010g0254a0001c0001t0094g0253 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1454+3510C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263046 | ||||||
chr2:157263107
|
G | A | 2 | a0002c0003t0004g0164a0002c0003t0028g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1454+3571G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263107 | ||||||
chr2:157263123
|
G | A | 1 | a0001c0001t0002g0025 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1454+3587G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263123 | ||||||
chr2:157263222
|
T | C | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3686T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263222 | ||||||
chr2:157263268
|
A | G | 2 | a0002c0005t0019g0199a0002c0005t0019g0200 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1454+3732A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263268 | ||||||
chr2:157263273
|
A | G | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+3737A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263273 | ||||||
chr2:157263422
|
G | A | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+3886G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263422 | ||||||
chr2:157263480
|
T | C | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+3944T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263480 | ||||||
chr2:157263670
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1454+4134C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263670 | ||||||
chr2:157263891
|
T | G | 2 | a0001c0001t0009g0151a0001c0001t0050g0149 | 2 | HG00438.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1454+4355T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263891 | ||||||
chr2:157263913
|
G | C | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256 | 3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1454+4377G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263913 | ||||||
chr2:157263962
|
A | G | 1 | a0001c0002t0086g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1454+4426A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157263962 | ||||||
chr2:157264122
|
T | C | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+4586T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264122 | ||||||
chr2:157264148
|
T | C | 1 | a0004c0006t0014g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1454+4612T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264148 | ||||||
chr2:157264174
|
T | TAC | 10 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0055others(7): Show | 10 | HG01106.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454+4667_1454+466 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | |||||
chr2:157264174
|
TAC | T | 15 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0033g0256others(12): Show | 15 | HG01123.hp2 HG02083.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1454+4667_1454+466 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | |||||
chr2:157264174
|
TACAC | T | 80 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0138others(77): Show | 83 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1454+4665_1454+466 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | |||||
chr2:157264174
|
TACACAC | T | 4 | a0001c0001t0001g0045a0001c0002t0010g0252a0001c0002t0076g0251others(1): Show | 4 | HG02258.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+4663_1454+466 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264174 | |||||
chr2:157264333
|
T | C | 1 | a0001c0001t0088g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1454+4797T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264333 | ||||||
chr2:157264414
|
C | A | 6 | a0002c0005t0002g0205a0002c0005t0003g0204a0002c0005t0017g0206others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+4878C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264414 | ||||||
chr2:157264456
|
C | T | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+4920C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264456 | ||||||
chr2:157264568
|
T | G | 2 | a0002c0003t0006g0173a0002c0003t0006g0174 | 2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1454+5032T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264568 | ||||||
chr2:157264597
|
GT | G | 17 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0080g0237others(14): Show | 18 | HG01074.hp2 HG02572.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1454+5070delT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157264597 | |||||
chr2:157264692
|
C | T | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+5156C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264692 | ||||||
chr2:157264953
|
C | T | 97 | a0001c0001t0001g0026a0001c0001t0001g0215a0001c0001t0010g0254others(94): Show | 100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1454+5417C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157264953 | ||||||
chr2:157265175
|
T | C | 70 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(67): Show | 72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1454+5639T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157265175 | ||||||
chr2:157265332
|
T | C | 1 | a0001c0001t0005g0028 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1454+5796T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157265332 | ||||||
chr2:157265806
|
C | T | 24 | a0001c0001t0001g0215a0001c0002t0002g0136a0003c0004t0001g0014others(21): Show | 25 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+6270C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157265806 | ||||||
chr2:157266192
|
T | C | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+6656T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266192 | ||||||
chr2:157266234
|
A | G | 1 | a0002c0005t0027g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1454+6698A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266234 | ||||||
chr2:157266241
|
T | G | 1 | a0001c0001t0050g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1454+6705T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266241 | ||||||
chr2:157266312
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1454+6776G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266312 | ||||||
chr2:157266417
|
C | T | 2 | a0001c0002t0096g0239a0001c0002t0098g0244 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1454+6881C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266417 | ||||||
chr2:157266509
|
A | G | 2 | a0001c0001t0010g0254a0001c0001t0094g0253 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1454+6973A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266509 | ||||||
chr2:157266792
|
C | T | 1 | a0002c0005t0002g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1454+7256C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266792 | ||||||
chr2:157266835
|
C | T | 2 | a0001c0002t0014g0258a0001c0002t0087g0259 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1454+7299C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157266835 | ||||||
chr2:157267019
|
C | G | 8 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0080g0237others(5): Show | 9 | HG01074.hp2 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1454+7483C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267019 | ||||||
chr2:157267020
|
A | G | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+7484A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267020 | ||||||
chr2:157267058
|
G | A | 71 | a0001c0001t0001g0215a0001c0001t0002g0057a0002c0003t0004g0164others(68): Show | 73 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1454+7522G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267058 | ||||||
chr2:157267180
|
G | C | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+7644G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267180 | ||||||
chr2:157267315
|
G | A | 1 | a0002c0003t0067g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1454+7779G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267315 | ||||||
chr2:157267482
|
A | G | 4 | a0005c0008t0004g0201a0005c0008t0018g0170a0005c0008t0026g0172others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+7946A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267482 | ||||||
chr2:157267765
|
C | T | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1454+8229C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267765 | ||||||
chr2:157267783
|
T | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0007c0012t0022g0137 | 3 | HG01123.hp2 HG01192.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1454+8247T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157267783 | ||||||
chr2:157268045
|
G | T | 10 | a0001c0001t0033g0256a0001c0001t0081g0241a0001c0001t0093g0243others(7): Show | 10 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454+8509G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268045 | ||||||
chr2:157268176
|
C | T | 1 | a0001c0001t0088g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1454+8640C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268176 | ||||||
chr2:157268375
|
T | A | 1 | a0001c0001t0028g0150 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1454+8839T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268375 | ||||||
chr2:157268401
|
G | A | 9 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0024g0060others(6): Show | 10 | HG01074.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454+8865G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268401 | ||||||
chr2:157268792
|
CCAAGA | C | 70 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(67): Show | 72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1454+9260_1454+926 others(9): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157268792 | |||||
chr2:157268793
|
CA | C | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+9259delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157268793 | |||||
chr2:157268826
|
T | C | 1 | a0001c0001t0029g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1454+9290T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268826 | ||||||
chr2:157268827
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1454+9291A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268827 | ||||||
chr2:157268932
|
C | T | 1 | a0003c0004t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1454+9396C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268932 | ||||||
chr2:157268999
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1454+9463C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157268999 | ||||||
chr2:157269077
|
T | C | 2 | a0001c0001t0015g0249a0001c0001t0015g0255 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1454+9541T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269077 | ||||||
chr2:157269199
|
C | T | 2 | a0001c0001t0002g0135a0001c0002t0003g0162 | 2 | HG02074.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1454+9663C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269199 | ||||||
chr2:157269263
|
A | G | 1 | a0001c0009t0025g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1454+9727A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269263 | ||||||
chr2:157269393
|
T | G | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+9857T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269393 | ||||||
chr2:157269918
|
C | T | 4 | a0001c0001t0009g0147a0001c0001t0029g0061a0001c0002t0001g0024others(1): Show | 4 | HG00544.hp2 HG02040.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454+10382C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269918 | ||||||
chr2:157269946
|
C | T | 97 | a0001c0001t0001g0026a0001c0001t0001g0215a0001c0001t0010g0254others(94): Show | 100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1454+10410C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269946 | ||||||
chr2:157269950
|
A | G | 19 | a0002c0003t0004g0192a0002c0003t0006g0173a0002c0003t0006g0174others(16): Show | 20 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454+10414A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157269950 | ||||||
chr2:157270006
|
A | T | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+10470A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270006 | ||||||
chr2:157270083
|
C | T | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0008c0013t0032g0261 | 3 | HG02109.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1454+10547C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270083 | ||||||
chr2:157270153
|
G | A | 11 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG00544.hp1 HG02071.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1454+10617G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270153 | ||||||
chr2:157270177
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1454+10641G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270177 | ||||||
chr2:157270389
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1454+10853C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270389 | ||||||
chr2:157270414
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1454+10878T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270414 | ||||||
chr2:157270606
|
G | A | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+11070G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157270606 | ||||||
chr2:157271032
|
C | T | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1454+11496C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271032 | ||||||
chr2:157271041
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0004g0139 | 2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1454+11505G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271041 | ||||||
chr2:157271048
|
G | A | 4 | a0005c0008t0004g0201a0005c0008t0018g0170a0005c0008t0026g0172others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+11512G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271048 | ||||||
chr2:157271102
|
CA | C | 53 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0002t0010g0252others(50): Show | 54 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(51): Show |
intron_variant | MODIFIER | c.1454+11580delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157271102 | |||||
chr2:157271214
|
T | C | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1454+11678T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271214 | ||||||
chr2:157271216
|
G | T | 1 | a0001c0001t0002g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1454+11680G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271216 | ||||||
chr2:157271322
|
T | A | 3 | a0001c0001t0001g0053a0001c0001t0005g0054a0001c0002t0001g0068 | 3 | HG02738.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1454+11786T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271322 | ||||||
chr2:157271719
|
G | A | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1454+12183G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271719 | ||||||
chr2:157271808
|
A | G | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1454+12272A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157271808 | ||||||
chr2:157272109
|
G | A | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-12173G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272109 | ||||||
chr2:157272121
|
T | C | 4 | a0005c0008t0004g0201a0005c0008t0018g0170a0005c0008t0026g0172others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-12161T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272121 | ||||||
chr2:157272247
|
G | A | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-12035G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272247 | ||||||
chr2:157272622
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-11660C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157272622 | ||||||
chr2:157273023
|
C | T | 1 | a0001c0001t0001g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1455-11259C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273023 | ||||||
chr2:157273477
|
A | G | 2 | a0001c0002t0014g0258a0001c0002t0087g0259 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1455-10805A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273477 | ||||||
chr2:157273520
|
A | G | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1455-10762A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273520 | ||||||
chr2:157273630
|
C | CT | 80 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 86 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1455-10623dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTT | 15 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0236others(12): Show | 15 | HG00621.hp1 HG00673.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1455-10624_1455-10 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTT | 12 | a0001c0001t0001g0215a0001c0001t0010g0254a0001c0001t0024g0060others(9): Show | 12 | HG00099.hp1 HG02083.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1455-10626_1455-10 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTT | 13 | a0001c0002t0031g0015a0002c0003t0006g0174a0003c0004t0001g0014others(10): Show | 15 | HG00597.hp2 HG00673.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1455-10627_1455-10 others(11): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTT | 8 | a0001c0001t0001g0026a0001c0002t0078g0247a0002c0003t0023g0188others(5): Show | 9 | HG00639.hp1 HG02071.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-10628_1455-10 others(12): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTTT | 12 | a0001c0001t0080g0237a0001c0002t0086g0248a0002c0003t0007g0209others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1455-10629_1455-10 others(13): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0088g0246a0002c0003t0004g0164a0002c0003t0004g0192others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1455-10630_1455-10 others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTTT others(2): Show |
11 | a0002c0003t0026g0166a0002c0003t0041g0195a0002c0003t0067g0165others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1455-10631_1455-10 others(15): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTTT others(3): Show |
12 | a0002c0003t0101g0196a0002c0005t0002g0205a0002c0005t0003g0204others(9): Show | 12 | HG01891.hp1 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1455-10632_1455-10 others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTTT others(4): Show |
2 | a0002c0005t0027g0207a0004c0006t0090g0185 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1455-10633_1455-10 others(17): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
C | CTTTTTTT others(5): Show |
1 | a0002c0003t0100g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1455-10634_1455-10 others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273630
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1455-10632_1455-10 others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157273630 | |||||
chr2:157273688
|
G | A | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-10594G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273688 | ||||||
chr2:157273750
|
C | T | 1 | a0004c0006t0014g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1455-10532C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273750 | ||||||
chr2:157273791
|
C | T | 2 | a0001c0001t0035g0004a0001c0001t0036g0004 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1455-10491C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273791 | ||||||
chr2:157273873
|
G | A | 2 | a0004c0011t0079g0176a0004c0011t0089g0177 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1455-10409G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273873 | ||||||
chr2:157273926
|
C | G | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-10356C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273926 | ||||||
chr2:157273967
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-10315C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273967 | ||||||
chr2:157273983
|
C | T | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-10299C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273983 | ||||||
chr2:157273986
|
C | A | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-10296C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157273986 | ||||||
chr2:157274124
|
T | C | 2 | a0001c0002t0091g0240a0001c0002t0092g0245 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1455-10158T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274124 | ||||||
chr2:157274225
|
T | C | 2 | a0002c0005t0044g0169a0002c0005t0064g0203 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1455-10057T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274225 | ||||||
chr2:157274229
|
C | T | 2 | a0002c0003t0007g0209a0002c0003t0024g0208 | 2 | HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1455-10053C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274229 | ||||||
chr2:157274638
|
C | CGT | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-9643_1455-964 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157274638 | |||||
chr2:157274955
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(65): Show | 74 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1455-9327C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274955 | ||||||
chr2:157274971
|
G | A | 1 | a0001c0001t0024g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1455-9311G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157274971 | ||||||
chr2:157275021
|
A | T | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-9261A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275021 | ||||||
chr2:157275068
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1455-9214C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275068 | ||||||
chr2:157275216
|
G | C | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-9066G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275216 | ||||||
chr2:157275287
|
G | A | 1 | a0004c0011t0079g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1455-8995G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275287 | ||||||
chr2:157275597
|
G | A | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0008c0013t0032g0261 | 3 | HG02109.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1455-8685G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275597 | ||||||
chr2:157275638
|
G | A | 2 | a0001c0001t0011g0109a0001c0001t0059g0049 | 2 | NA19064.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1455-8644G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275638 | ||||||
chr2:157275722
|
T | G | 1 | a0001c0001t0082g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1455-8560T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275722 | ||||||
chr2:157275769
|
A | C | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-8513A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275769 | ||||||
chr2:157275788
|
T | A | 2 | a0002c0003t0004g0164a0002c0003t0028g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1455-8494T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275788 | ||||||
chr2:157275810
|
C | G | 1 | a0003c0004t0002g0227 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1455-8472C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157275810 | ||||||
chr2:157276064
|
A | T | 1 | a0002c0005t0017g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1455-8218A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276064 | ||||||
chr2:157276114
|
G | A | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-8168G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276114 | ||||||
chr2:157276321
|
G | A | 1 | a0003c0007t0002g0212 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1455-7961G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276321 | ||||||
chr2:157276361
|
T | C | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7921T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276361 | ||||||
chr2:157276362
|
G | T | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7920G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276362 | ||||||
chr2:157276369
|
G | C | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7913G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276369 | ||||||
chr2:157276460
|
T | C | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-7822T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276460 | ||||||
chr2:157276578
|
T | C | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-7704T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276578 | ||||||
chr2:157276580
|
C | A | 1 | a0001c0001t0011g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1455-7702C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276580 | ||||||
chr2:157276637
|
G | A | 2 | a0002c0003t0004g0164a0002c0003t0028g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1455-7645G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276637 | ||||||
chr2:157276671
|
T | C | 2 | a0001c0001t0015g0249a0001c0001t0015g0255 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1455-7611T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276671 | ||||||
chr2:157276780
|
T | TTCATTGA others(277): Show |
3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-7499_1455-749 others(288): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157276780 | |||||
chr2:157276784
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-7498C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276784 | ||||||
chr2:157276888
|
G | C | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-7394G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157276888 | ||||||
chr2:157277033
|
G | A | 3 | a0001c0001t0002g0057a0001c0001t0002g0135a0001c0001t0002g0145 | 3 | NA18941.hp1 NA18963.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1455-7249G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277033 | ||||||
chr2:157277091
|
T | C | 1 | a0003c0004t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1455-7191T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277091 | ||||||
chr2:157277107
|
T | A | 1 | a0001c0002t0031g0015 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1455-7175T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277107 | ||||||
chr2:157277253
|
A | T | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-7029A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277253 | ||||||
chr2:157277271
|
T | C | 41 | a0002c0003t0004g0192a0002c0003t0006g0173a0002c0003t0006g0174others(38): Show | 42 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.1455-7011T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277271 | ||||||
chr2:157277278
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0002g0098 | 2 | HG01496.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1455-7004C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277278 | ||||||
chr2:157277288
|
T | A | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-6994T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277288 | ||||||
chr2:157277343
|
G | C | 1 | a0001c0001t0048g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1455-6939G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277343 | ||||||
chr2:157277392
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1455-6890A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277392 | ||||||
chr2:157277546
|
G | C | 7 | a0001c0001t0001g0072a0001c0001t0002g0003a0001c0001t0004g0069others(4): Show | 9 | HG00280.hp2 HG00639.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-6736G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277546 | ||||||
chr2:157277605
|
G | C | 3 | a0001c0001t0010g0254a0001c0001t0094g0253a0001c0002t0031g0015 | 4 | HG02895.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455-6677G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277605 | ||||||
chr2:157277691
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0080g0237 | 2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1455-6591C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277691 | ||||||
chr2:157277802
|
G | A | 10 | a0001c0001t0033g0256a0001c0001t0081g0241a0001c0001t0093g0243others(7): Show | 10 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1455-6480G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277802 | ||||||
chr2:157277837
|
G | T | 20 | a0002c0005t0002g0205a0002c0005t0003g0204a0002c0005t0017g0206others(17): Show | 20 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1455-6445G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277837 | ||||||
chr2:157277917
|
C | T | 1 | a0002c0003t0023g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1455-6365C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157277917 | ||||||
chr2:157278317
|
A | C | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-5965A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278317 | ||||||
chr2:157278328
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(85): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1455-5954T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278328 | ||||||
chr2:157278417
|
T | C | 1 | a0001c0001t0049g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1455-5865T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278417 | ||||||
chr2:157278419
|
G | A | 1 | a0002c0005t0044g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455-5863G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278419 | ||||||
chr2:157278668
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-5614C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278668 | ||||||
chr2:157278691
|
G | A | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-5591G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278691 | ||||||
chr2:157278718
|
T | C | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-5564T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278718 | ||||||
chr2:157278947
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1455-5335G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157278947 | ||||||
chr2:157279286
|
C | T | 1 | a0001c0001t0093g0243 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1455-4996C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279286 | ||||||
chr2:157279298
|
G | A | 70 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(67): Show | 72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-4984G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279298 | ||||||
chr2:157279318
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1455-4964G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279318 | ||||||
chr2:157279326
|
G | A | 70 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(67): Show | 72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-4956G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279326 | ||||||
chr2:157279468
|
C | T | 43 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(40): Show | 44 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.1455-4814C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279468 | ||||||
chr2:157279481
|
C | A | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-4801C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279481 | ||||||
chr2:157279530
|
G | A | 1 | a0001c0001t0029g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1455-4752G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279530 | ||||||
chr2:157279718
|
T | A | 1 | a0001c0001t0030g0035 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1455-4564T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279718 | ||||||
chr2:157279767
|
C | T | 1 | a0001c0002t0010g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1455-4515C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279767 | ||||||
chr2:157279768
|
G | A | 70 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(67): Show | 72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-4514G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279768 | ||||||
chr2:157279831
|
T | C | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-4451T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279831 | ||||||
chr2:157279889
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1455-4393G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279889 | ||||||
chr2:157279943
|
C | T | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-4339C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279943 | ||||||
chr2:157279992
|
T | C | 1 | a0001c0001t0075g0074 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1455-4290T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157279992 | ||||||
chr2:157280003
|
C | G | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-4279C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280003 | ||||||
chr2:157280053
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-4229C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280053 | ||||||
chr2:157280421
|
C | T | 47 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(44): Show | 48 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1455-3861C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280421 | ||||||
chr2:157280437
|
A | G | 1 | a0001c0001t0005g0097 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1455-3845A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280437 | ||||||
chr2:157280491
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-3791C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280491 | ||||||
chr2:157280531
|
A | G | 3 | a0001c0001t0033g0256a0001c0001t0095g0238a0001c0001t0097g0242 | 3 | HG03225.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1455-3751A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280531 | ||||||
chr2:157280755
|
G | C | 4 | a0005c0008t0004g0201a0005c0008t0018g0170a0005c0008t0026g0172others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-3527G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280755 | ||||||
chr2:157280915
|
C | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-3367C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280915 | ||||||
chr2:157280973
|
G | C | 2 | a0001c0002t0096g0239a0001c0002t0098g0244 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1455-3309G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280973 | ||||||
chr2:157280990
|
C | T | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-3292C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157280990 | ||||||
chr2:157281004
|
G | A | 2 | a0001c0002t0014g0258a0001c0002t0087g0259 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1455-3278G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281004 | ||||||
chr2:157281114
|
C | T | 97 | a0001c0001t0001g0026a0001c0001t0001g0215a0001c0001t0010g0254others(94): Show | 100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1455-3168C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281114 | ||||||
chr2:157281115
|
A | G | 97 | a0001c0001t0001g0026a0001c0001t0001g0215a0001c0001t0010g0254others(94): Show | 100 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1455-3167A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281115 | ||||||
chr2:157281218
|
C | T | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-3064C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281218 | ||||||
chr2:157281219
|
G | A | 1 | a0002c0005t0012g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1455-3063G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281219 | ||||||
chr2:157281272
|
C | T | 70 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(67): Show | 72 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1455-3010C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281272 | ||||||
chr2:157281421
|
C | T | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455-2861C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281421 | ||||||
chr2:157281532
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0080g0237 | 2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1455-2750C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281532 | ||||||
chr2:157281563
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1455-2719C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281563 | ||||||
chr2:157281612
|
A | G | 1 | a0001c0001t0037g0132 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1455-2670A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281612 | ||||||
chr2:157281612
|
AAAAG | A | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455-2653_1455-265 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157281612 | |||||
chr2:157281919
|
C | T | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455-2363C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157281919 | ||||||
chr2:157282079
|
A | G | 3 | a0001c0002t0010g0252a0001c0002t0076g0251a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1455-2203A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282079 | ||||||
chr2:157282079
|
A | T | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-2203A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282079 | ||||||
chr2:157282133
|
C | T | 48 | a0001c0001t0002g0042a0002c0003t0004g0164a0002c0003t0004g0192others(45): Show | 49 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(46): Show |
intron_variant | MODIFIER | c.1455-2149C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282133 | ||||||
chr2:157282162
|
A | T | 2 | a0002c0003t0007g0209a0002c0003t0024g0208 | 2 | HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1455-2120A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282162 | ||||||
chr2:157282226
|
TA | T | 5 | a0001c0001t0002g0025a0001c0001t0002g0135a0001c0002t0010g0252others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1455-2055delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282226 | ||||||
chr2:157282227
|
A | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(86): Show | 96 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1455-2055A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282227 | ||||||
chr2:157282253
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0080g0237others(5): Show | 9 | HG01074.hp2 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-2029A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282253 | ||||||
chr2:157282298
|
CCAAT | C | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1979_1455-197 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157282298 | |||||
chr2:157282337
|
G | T | 27 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(24): Show | 28 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1455-1945G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282337 | ||||||
chr2:157282654
|
A | T | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1628A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282654 | ||||||
chr2:157282719
|
C | A | 24 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0015g0249others(21): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455-1563C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282719 | ||||||
chr2:157282733
|
C | CA | 67 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(64): Show | 69 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1455-1541dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 157282733 | |||||
chr2:157282991
|
G | A | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1291G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157282991 | ||||||
chr2:157283000
|
A | T | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1455-1282A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283000 | ||||||
chr2:157283142
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1455-1140T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283142 | ||||||
chr2:157283329
|
G | A | 8 | a0001c0001t0001g0026a0001c0001t0010g0254a0001c0001t0080g0237others(5): Show | 9 | HG01074.hp2 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-953G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283329 | ||||||
chr2:157283331
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1455-951G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283331 | ||||||
chr2:157283354
|
T | C | 73 | a0001c0001t0001g0215a0001c0001t0088g0246a0001c0002t0078g0247others(70): Show | 75 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-928T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283354 | ||||||
chr2:157283598
|
T | C | 3 | a0001c0001t0033g0256a0001c0001t0095g0238a0001c0001t0097g0242 | 3 | HG03225.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1455-684T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283598 | ||||||
chr2:157283652
|
T | C | 1 | a0005c0008t0004g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1455-630T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283652 | ||||||
chr2:157283696
|
AC | A | 69 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(66): Show | 71 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1455-585delC | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283696 | ||||||
chr2:157283852
|
C | T | 1 | a0002c0003t0061g0194 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1455-430C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157283852 | ||||||
chr2:157284112
|
A | G | 2 | a0001c0001t0015g0249a0001c0001t0015g0255 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1455-170A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157284112 | ||||||
chr2:157284205
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(92): Show | 102 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1455-77C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 1/9 | chr2 | 157284205 | ||||||
chr2:157284459
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1621+11C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284459 | ||||||
chr2:157284559
|
C | T | 69 | a0001c0001t0001g0215a0002c0003t0004g0164a0002c0003t0004g0192others(66): Show | 71 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1621+111C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284559 | ||||||
chr2:157284567
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(76): Show | 85 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1621+119T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284567 | ||||||
chr2:157284580
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1621+132G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284580 | ||||||
chr2:157284580
|
G | T | 46 | a0002c0003t0004g0164a0002c0003t0004g0192a0002c0003t0006g0173others(43): Show | 47 | HG00639.hp1 HG00735.hp2 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.1621+132G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284580 | ||||||
chr2:157284612
|
A | G | 1 | a0001c0001t0005g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1621+164A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284612 | ||||||
chr2:157284618
|
G | A | 1 | a0001c0002t0099g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1621+170G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284618 | ||||||
chr2:157284650
|
T | C | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1621+202T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284650 | ||||||
chr2:157284674
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(91): Show | 99 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1621+226C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284674 | ||||||
chr2:157284769
|
G | T | 23 | a0001c0001t0001g0215a0003c0004t0001g0014a0003c0004t0001g0213others(20): Show | 24 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1621+321G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284769 | ||||||
chr2:157284790
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1621+342C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157284790 | ||||||
chr2:157285175
|
T | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(88): Show | 98 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1621+727T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285175 | ||||||
chr2:157285241
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(163): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1622-774T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285241 | ||||||
chr2:157285437
|
G | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0016others(90): Show | 100 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1622-578G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285437 | ||||||
chr2:157285509
|
G | A | 1 | a0002c0005t0027g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-506G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285509 | ||||||
chr2:157285577
|
G | A | 1 | a0001c0002t0031g0015 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1622-438G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285577 | ||||||
chr2:157285619
|
T | C | 2 | a0002c0003t0004g0164a0002c0003t0028g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1622-396T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285619 | ||||||
chr2:157285663
|
G | A | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-352G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285663 | ||||||
chr2:157285974
|
T | C | 3 | a0001c0001t0088g0246a0001c0002t0078g0247a0001c0002t0086g0248 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1622-41T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157285974 | ||||||
chr2:157286004
|
C | T | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-11C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 2/9 | chr2 | 157286004 | ||||||
chr2:157286241
|
C | T | 2 | a0002c0005t0012g0013a0002c0005t0012g0187 | 3 | HG02258.hp2 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1741+107C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286241 | ||||||
chr2:157286301
|
CAT | C | 7 | a0001c0001t0001g0016a0001c0001t0002g0042a0001c0001t0003g0001others(4): Show | 10 | HG01361.hp1 HG01433.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1741+169_1741+170d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286301 | |||||
chr2:157286634
|
G | A | 1 | a0001c0001t0016g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1741+500G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286634 | ||||||
chr2:157286737
|
C | T | 2 | a0001c0002t0091g0240a0001c0002t0092g0245 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1741+603C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286737 | ||||||
chr2:157286872
|
C | A | 2 | a0001c0002t0091g0240a0001c0002t0092g0245 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1741+738C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157286872 | ||||||
chr2:157286893
|
A | AGT | 41 | a0001c0001t0001g0031a0001c0001t0001g0107a0001c0001t0001g0144others(38): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1741+802_1741+803d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
A | AGTGT | 31 | a0001c0001t0001g0055a0001c0001t0003g0033a0001c0001t0054g0021others(28): Show | 32 | HG00639.hp1 HG00735.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1741+800_1741+803d others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
A | AGTGTGT | 4 | a0001c0001t0001g0072a0001c0001t0004g0071a0002c0005t0002g0205others(1): Show | 4 | HG01891.hp1 HG02074.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+798_1741+803d others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
A | AGTGTGTG others(5): Show |
1 | a0001c0002t0014g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1741+792_1741+803d others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
A | AGTGTGTG others(9): Show |
1 | a0001c0002t0087g0259 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1741+788_1741+803d others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
AGT | A | 28 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0062others(25): Show | 29 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1741+802_1741+803d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
AGTGT | A | 49 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0075others(46): Show | 51 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1741+800_1741+803d others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
AGTGTGT | A | 5 | a0001c0001t0002g0114a0001c0001t0015g0249a0001c0001t0015g0255others(2): Show | 5 | HG00280.hp1 HG00438.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1741+798_1741+803d others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+790_1741+803d others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157286893
|
AGTGTGTG others(9): Show |
A | 3 | a0001c0001t0082g0260a0001c0002t0010g0252a0001c0002t0077g0250 | 3 | HG02258.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1741+788_1741+803d others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157286893 | |||||
chr2:157287097
|
T | A | 2 | a0002c0003t0004g0164a0002c0003t0028g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1741+963T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287097 | ||||||
chr2:157287129
|
A | G | 1 | a0001c0001t0005g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1741+995A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287129 | ||||||
chr2:157287237
|
T | C | 1 | a0002c0003t0042g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1741+1103T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287237 | ||||||
chr2:157287246
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1741+1112C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287246 | ||||||
chr2:157287251
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1741+1117G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287251 | ||||||
chr2:157287272
|
T | C | 1 | a0003c0007t0002g0212 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1741+1138T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287272 | ||||||
chr2:157287295
|
A | C | 2 | a0002c0003t0041g0195a0002c0003t0067g0165 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1741+1161A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287295 | ||||||
chr2:157287339
|
T | C | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0082g0260 | 3 | HG02622.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1741+1205T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287339 | ||||||
chr2:157287422
|
T | A | 2 | a0004c0011t0079g0176a0004c0011t0089g0177 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1741+1288T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287422 | ||||||
chr2:157287423
|
C | T | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0082g0260 | 3 | HG02622.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1741+1289C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287423 | ||||||
chr2:157287682
|
C | T | 11 | a0001c0002t0010g0252a0001c0002t0077g0250a0002c0003t0004g0164others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1741+1548C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287682 | ||||||
chr2:157287683
|
G | A | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1741+1549G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287683 | ||||||
chr2:157287746
|
T | A | 1 | a0001c0001t0011g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1741+1612T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287746 | ||||||
chr2:157287757
|
A | T | 32 | a0001c0001t0002g0057a0001c0001t0069g0094a0001c0002t0001g0067others(29): Show | 33 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1741+1623A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287757 | ||||||
chr2:157287797
|
A | G | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1741+1663A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287797 | ||||||
chr2:157287845
|
A | G | 31 | a0001c0001t0002g0057a0001c0001t0069g0094a0001c0002t0001g0067others(28): Show | 32 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1741+1711A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287845 | ||||||
chr2:157287878
|
A | C | 1 | a0003c0007t0002g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1741+1744A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287878 | ||||||
chr2:157287884
|
T | C | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1741+1750T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157287884 | ||||||
chr2:157288192
|
T | C | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1741+2058T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288192 | ||||||
chr2:157288253
|
T | C | 1 | a0001c0002t0002g0136 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1741+2119T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288253 | ||||||
chr2:157288270
|
A | G | 57 | a0001c0001t0010g0254a0001c0002t0001g0067a0001c0002t0001g0073others(54): Show | 59 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(56): Show |
intron_variant | MODIFIER | c.1741+2136A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288270 | ||||||
chr2:157288401
|
C | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1741+2267C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288401 | ||||||
chr2:157288480
|
A | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | NA18977.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1741+2346A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288480 | ||||||
chr2:157288579
|
G | T | 1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+2445G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288579 | ||||||
chr2:157288592
|
GATTC | G | 7 | a0004c0006t0010g0178a0004c0006t0013g0179a0004c0006t0013g0180others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1741+2462_1741+246 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157288592 | |||||
chr2:157288697
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0153 | 2 | HG02074.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1741+2563T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288697 | ||||||
chr2:157288731
|
G | A | 1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+2597G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288731 | ||||||
chr2:157288731
|
G | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1741+2597G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288731 | ||||||
chr2:157288747
|
C | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0063 | 2 | NA19064.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1741+2613C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288747 | ||||||
chr2:157288865
|
C | T | 1 | a0001c0002t0014g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1741+2731C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288865 | ||||||
chr2:157288877
|
T | C | 33 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(30): Show | 34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1741+2743T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288877 | ||||||
chr2:157288906
|
G | A | 1 | a0001c0002t0078g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1741+2772G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288906 | ||||||
chr2:157288913
|
A | C | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1741+2779A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288913 | ||||||
chr2:157288927
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1741+2793A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288927 | ||||||
chr2:157288931
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0020 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1741+2797G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288931 | ||||||
chr2:157288935
|
G | A | 1 | a0005c0008t0018g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1741+2801G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157288935 | ||||||
chr2:157289136
|
C | A | 1 | a0002c0003t0008g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1741+3002C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289136 | ||||||
chr2:157289146
|
GCA | G | 59 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(56): Show | 61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1741+3015_1741+301 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157289146 | |||||
chr2:157289318
|
T | A | 1 | a0001c0001t0040g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1741+3184T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289318 | ||||||
chr2:157289422
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1741+3288A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289422 | ||||||
chr2:157289462
|
A | T | 3 | a0001c0009t0025g0009a0001c0009t0025g0134a0001c0009t0071g0009 | 3 | HG02896.hp1 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1741+3328A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289462 | ||||||
chr2:157289571
|
C | T | 59 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(56): Show | 61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1741+3437C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289571 | ||||||
chr2:157289674
|
T | C | 4 | a0001c0002t0001g0073a0001c0002t0002g0123a0003c0004t0018g0219others(1): Show | 4 | NA18982.hp2 NA18985.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1741+3540T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289674 | ||||||
chr2:157289710
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0050others(16): Show | 19 | HG00597.hp1 HG00609.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1741+3576A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289710 | ||||||
chr2:157289751
|
A | G | 33 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(30): Show | 34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1741+3617A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289751 | ||||||
chr2:157289787
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1741+3653T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157289787 | ||||||
chr2:157290062
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1741+3928A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290062 | ||||||
chr2:157290073
|
C | CA | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+3951dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290073 | |||||
chr2:157290080
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0009g0011 | 2 | NA19003.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1741+3946A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290080 | ||||||
chr2:157290083
|
AAATGTAT | A | 8 | a0001c0001t0001g0008a0001c0001t0002g0046a0001c0001t0002g0104others(5): Show | 8 | HG00621.hp2 HG02027.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741+3951_1741+395 others(11): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290083 | |||||
chr2:157290084
|
A | AAAATATA others(3): Show |
1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+3951_1741+395 others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290084 | |||||
chr2:157290087
|
G | A | 1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1741+3953G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290087 | ||||||
chr2:157290087
|
G | GTA | 3 | a0001c0002t0002g0136a0001c0002t0031g0015a0004c0006t0085g0181 | 4 | HG01256.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+3978_1741+397 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | |||||
chr2:157290087
|
GTA | G | 5 | a0002c0005t0012g0013a0002c0005t0012g0187a0002c0005t0019g0199others(2): Show | 6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3978_1741+397 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | |||||
chr2:157290087
|
GTATA | G | 18 | a0001c0001t0001g0215a0001c0001t0010g0254a0001c0001t0016g0113others(15): Show | 18 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1741+3976_1741+397 others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | |||||
chr2:157290087
|
GTATATA | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(171): Show | 180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1741+3974_1741+397 others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290087 | |||||
chr2:157290093
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0002g0046a0001c0001t0002g0104others(5): Show | 8 | HG00621.hp2 HG02027.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741+3959A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290093 | ||||||
chr2:157290095
|
A | T | 14 | a0001c0001t0010g0254a0001c0001t0080g0237a0001c0001t0094g0253others(11): Show | 14 | HG00639.hp1 HG01074.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741+3961A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290095 | ||||||
chr2:157290099
|
A | G | 9 | a0001c0002t0034g0093a0002c0005t0002g0198a0004c0006t0010g0178others(6): Show | 9 | HG01884.hp1 HG02602.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1741+3965A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290099 | ||||||
chr2:157290108
|
T | C | 5 | a0002c0005t0012g0013a0002c0005t0012g0187a0002c0005t0019g0199others(2): Show | 6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3974T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290108 | ||||||
chr2:157290110
|
T | C | 5 | a0002c0005t0012g0013a0002c0005t0012g0187a0002c0005t0019g0199others(2): Show | 6 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3976T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290110 | ||||||
chr2:157290112
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1741+3978T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290112 | ||||||
chr2:157290112
|
T | TATATATA others(5): Show |
1 | a0001c0002t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(7): Show |
6 | a0003c0004t0001g0224a0003c0004t0001g0229a0003c0004t0002g0214others(3): Show | 6 | HG00673.hp1 HG02071.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(7): Show |
8 | a0001c0002t0003g0162a0001c0002t0021g0051a0003c0004t0001g0014others(5): Show | 9 | HG00597.hp2 HG02074.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(18): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(9): Show |
6 | a0001c0002t0001g0024a0001c0002t0001g0073a0001c0002t0001g0133others(3): Show | 6 | NA18960.hp2 NA18977.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(20): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(11): Show |
2 | a0002c0005t0002g0205a0002c0005t0003g0204 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(22): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(11): Show |
5 | a0001c0002t0002g0158a0001c0002t0030g0032a0002c0005t0027g0207others(2): Show | 5 | HG02165.hp2 HG02257.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(22): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(13): Show |
2 | a0001c0002t0098g0244a0003c0004t0002g0227 | 2 | HG02970.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(24): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(15): Show |
3 | a0001c0002t0091g0240a0001c0002t0092g0245a0001c0002t0096g0239 | 3 | HG02572.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(26): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(19): Show |
3 | a0001c0002t0010g0252a0001c0002t0077g0250a0004c0006t0090g0185 | 3 | HG01884.hp1 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(30): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(21): Show |
2 | a0001c0002t0047g0092a0004c0006t0013g0180 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(32): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(23): Show |
1 | a0001c0002t0086g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(19): Show |
1 | a0001c0002t0099g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(30): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(21): Show |
1 | a0002c0005t0027g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(32): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(23): Show |
3 | a0001c0002t0066g0096a0002c0005t0002g0198a0004c0006t0014g0168 | 3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(23): Show |
1 | a0002c0005t0064g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(25): Show |
1 | a0004c0006t0013g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(36): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(23): Show |
1 | a0001c0002t0087g0259 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(34): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(25): Show |
1 | a0002c0005t0017g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(36): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(27): Show |
3 | a0004c0006t0010g0178a0004c0006t0013g0179a0004c0006t0014g0183 | 3 | HG02723.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1741+3979_1741+398 others(38): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(29): Show |
1 | a0001c0002t0078g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(40): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290112
|
T | TATATATA others(29): Show |
1 | a0001c0002t0034g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1741+3979_1741+398 others(40): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290112 | |||||
chr2:157290116
|
T | C | 1 | a0004c0006t0013g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1741+3982T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290116 | ||||||
chr2:157290134
|
C | CAT | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+4007_1741+400 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157290134 | |||||
chr2:157290164
|
T | C | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+4030T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290164 | ||||||
chr2:157290175
|
A | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1741+4041A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290175 | ||||||
chr2:157290347
|
G | A | 1 | a0002c0005t0064g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1741+4213G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290347 | ||||||
chr2:157290450
|
G | T | 2 | a0001c0001t0004g0103a0001c0001t0006g0048 | 2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1741+4316G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290450 | ||||||
chr2:157290668
|
C | G | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741+4534C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290668 | ||||||
chr2:157290804
|
G | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1741+4670G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157290804 | ||||||
chr2:157291070
|
C | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1742-4593C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291070 | ||||||
chr2:157291252
|
T | C | 1 | a0001c0002t0014g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1742-4411T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291252 | ||||||
chr2:157291269
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0155 | 2 | HG03239.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1742-4394C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291269 | ||||||
chr2:157291432
|
C | T | 3 | a0001c0002t0076g0251a0001c0002t0087g0259a0001c0002t0099g0257 | 3 | HG02723.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-4231C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291432 | ||||||
chr2:157291474
|
C | T | 1 | a0003c0007t0003g0225 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1742-4189C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291474 | ||||||
chr2:157291633
|
A | AC | 183 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(180): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1742-4021dupC | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157291633 | |||||
chr2:157291633
|
A | ACC | 17 | a0001c0001t0001g0072a0001c0001t0003g0018a0001c0001t0003g0036others(14): Show | 18 | HG01433.hp2 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1742-4022_1742-402 others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157291633 | |||||
chr2:157291637
|
C | A | 2 | a0002c0003t0026g0166a0002c0003t0072g0167 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1742-4026C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291637 | ||||||
chr2:157291640
|
C | CT | 4 | a0001c0002t0001g0073a0001c0002t0002g0123a0003c0004t0018g0219others(1): Show | 4 | NA18982.hp2 NA18985.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1742-4023_1742-402 others(5): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291640 | ||||||
chr2:157291655
|
T | C | 30 | a0001c0001t0001g0102a0001c0002t0001g0024a0001c0002t0001g0067others(27): Show | 31 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1742-4008T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291655 | ||||||
chr2:157291843
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1742-3820T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291843 | ||||||
chr2:157291947
|
C | A | 3 | a0001c0002t0076g0251a0001c0002t0087g0259a0001c0002t0099g0257 | 3 | HG02723.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-3716C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157291947 | ||||||
chr2:157292125
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0009g0008 | 2 | HG00621.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1742-3538T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292125 | ||||||
chr2:157292200
|
G | C | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1742-3463G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292200 | ||||||
chr2:157292321
|
A | G | 3 | a0001c0002t0076g0251a0001c0002t0087g0259a0001c0002t0099g0257 | 3 | HG02723.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-3342A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292321 | ||||||
chr2:157292365
|
C | T | 2 | a0001c0002t0031g0015a0004c0006t0085g0181 | 3 | HG02895.hp2 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1742-3298C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292365 | ||||||
chr2:157292712
|
A | AT | 27 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(24): Show | 28 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1742-2939dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157292712 | |||||
chr2:157292715
|
T | A | 3 | a0001c0001t0001g0148a0001c0002t0091g0240a0001c0002t0092g0245 | 3 | HG01358.hp1 HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1742-2948T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292715 | ||||||
chr2:157292861
|
G | A | 2 | a0002c0003t0004g0164a0002c0003t0028g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1742-2802G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292861 | ||||||
chr2:157292866
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1742-2797A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292866 | ||||||
chr2:157292871
|
T | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1742-2792T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292871 | ||||||
chr2:157292998
|
G | C | 1 | a0001c0001t0075g0074 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1742-2665G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157292998 | ||||||
chr2:157293246
|
A | G | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-2417A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293246 | ||||||
chr2:157293275
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0035g0004a0001c0001t0036g0004 | 3 | HG00099.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1742-2388G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293275 | ||||||
chr2:157293279
|
C | T | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1742-2384C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293279 | ||||||
chr2:157293464
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1742-2199G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293464 | ||||||
chr2:157293503
|
A | G | 59 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(56): Show | 61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1742-2160A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293503 | ||||||
chr2:157293534
|
A | G | 32 | a0001c0001t0010g0254a0001c0001t0015g0249a0001c0001t0015g0255others(29): Show | 32 | HG00639.hp1 HG01074.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1742-2129A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293534 | ||||||
chr2:157293605
|
C | A | 1 | a0001c0001t0006g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1742-2058C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293605 | ||||||
chr2:157293606
|
C | G | 1 | a0001c0001t0006g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1742-2057C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293606 | ||||||
chr2:157293764
|
AG | A | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1742-1898delG | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293764 | ||||||
chr2:157293797
|
C | G | 1 | a0001c0001t0082g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1742-1866C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293797 | ||||||
chr2:157293839
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1742-1824C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293839 | ||||||
chr2:157293884
|
T | G | 1 | a0002c0003t0061g0194 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1742-1779T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293884 | ||||||
chr2:157293932
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1742-1731T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293932 | ||||||
chr2:157293988
|
G | A | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-1675G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157293988 | ||||||
chr2:157294248
|
C | T | 1 | a0002c0005t0017g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1742-1415C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294248 | ||||||
chr2:157294500
|
G | A | 1 | a0002c0003t0004g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1742-1163G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294500 | ||||||
chr2:157294504
|
T | G | 1 | a0002c0003t0004g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1742-1159T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294504 | ||||||
chr2:157294553
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1742-1110A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294553 | ||||||
chr2:157294608
|
C | T | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-1055C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294608 | ||||||
chr2:157294674
|
G | A | 2 | a0002c0003t0100g0197a0002c0003t0101g0196 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1742-989G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294674 | ||||||
chr2:157294694
|
G | A | 2 | a0001c0002t0010g0252a0001c0002t0077g0250 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1742-969G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294694 | ||||||
chr2:157294784
|
C | CCA | 3 | a0001c0002t0001g0068a0001c0002t0002g0078a0001c0002t0076g0251 | 3 | HG01943.hp2 HG02723.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1742-841_1742-840d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCA | C | 11 | a0001c0002t0001g0073a0001c0002t0021g0051a0001c0002t0091g0240others(8): Show | 11 | HG00673.hp1 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1742-841_1742-840d others(4): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACA | C | 23 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0123others(20): Show | 25 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1742-843_1742-840d others(6): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACACA | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0026others(45): Show | 54 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1742-845_1742-840d others(8): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACACAC others(1): Show |
C | 130 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(127): Show | 130 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1742-847_1742-840d others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACACAC others(3): Show |
C | 8 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0046g0106others(5): Show | 8 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1742-849_1742-840d others(12): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACACAC others(5): Show |
C | 18 | a0001c0001t0001g0010a0001c0001t0010g0254a0001c0001t0048g0070others(15): Show | 18 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1742-851_1742-840d others(14): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACACAC others(7): Show |
C | 4 | a0001c0001t0073g0087a0004c0011t0079g0176a0004c0011t0089g0177others(1): Show | 4 | HG01891.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1742-853_1742-840d others(16): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294784
|
CCACACAC others(11): Show |
C | 2 | a0002c0003t0100g0197a0002c0003t0101g0196 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1742-857_1742-840d others(20): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294784 | |||||
chr2:157294827
|
A | G | 1 | a0001c0001t0005g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1742-836A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294827 | ||||||
chr2:157294941
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1742-722C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157294941 | ||||||
chr2:157294965
|
C | CT | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1742-688dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157294965 | |||||
chr2:157295092
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1742-571G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295092 | ||||||
chr2:157295100
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1742-563G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295100 | ||||||
chr2:157295157
|
T | TC | 30 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(27): Show | 31 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1742-502dupC | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157295157 | |||||
chr2:157295202
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1742-461T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295202 | ||||||
chr2:157295435
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0129a0001c0001t0001g0235 | 3 | NA18947.hp1 NA18959.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1742-228A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295435 | ||||||
chr2:157295517
|
T | C | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1742-146T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295517 | ||||||
chr2:157295534
|
GA | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1742-116delA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 157295534 | |||||
chr2:157295608
|
C | T | 4 | a0001c0001t0024g0060a0001c0001t0097g0242a0002c0003t0004g0164others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1742-55C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 3/9 | chr2 | 157295608 | ||||||
chr2:157296145
|
A | AT | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1878-241dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 157296145 | |||||
chr2:157296962
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1997+449G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157296962 | ||||||
chr2:157297163
|
T | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0002g0066others(4): Show | 7 | HG00544.hp1 NA18968.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1997+650T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297163 | ||||||
chr2:157297173
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | NA18977.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1997+660T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297173 | ||||||
chr2:157297233
|
C | A | 1 | a0001c0002t0014g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1997+720C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297233 | ||||||
chr2:157297337
|
A | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | NA18977.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1997+824A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297337 | ||||||
chr2:157297464
|
G | A | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1997+951G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297464 | ||||||
chr2:157297498
|
C | G | 59 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(56): Show | 61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.1997+985C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297498 | ||||||
chr2:157297534
|
T | C | 3 | a0002c0005t0019g0199a0002c0005t0019g0200a0002c0005t0044g0169 | 3 | HG02486.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1997+1021T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297534 | ||||||
chr2:157297694
|
G | A | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1997+1181G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297694 | ||||||
chr2:157297718
|
G | T | 2 | a0001c0002t0078g0247a0001c0002t0086g0248 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1997+1205G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297718 | ||||||
chr2:157297831
|
C | T | 28 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(25): Show | 29 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1997+1318C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157297831 | ||||||
chr2:157298106
|
G | A | 2 | a0001c0001t0002g0104a0003c0007t0003g0225 | 2 | NA18948.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1998-1442G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298106 | ||||||
chr2:157298280
|
A | C | 2 | a0001c0001t0004g0103a0001c0001t0006g0048 | 2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1998-1268A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298280 | ||||||
chr2:157298294
|
A | G | 2 | a0001c0002t0078g0247a0001c0002t0086g0248 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1998-1254A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298294 | ||||||
chr2:157298414
|
G | A | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1998-1134G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298414 | ||||||
chr2:157298514
|
C | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1998-1034C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298514 | ||||||
chr2:157298544
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1998-1004A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298544 | ||||||
chr2:157298739
|
T | A | 198 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1998-809T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298739 | ||||||
chr2:157298782
|
G | A | 1 | a0001c0001t0082g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1998-766G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298782 | ||||||
chr2:157298912
|
C | T | 2 | a0001c0001t0046g0106a0001c0001t0048g0070 | 2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1998-636C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298912 | ||||||
chr2:157298926
|
T | C | 6 | a0002c0003t0041g0195a0002c0003t0067g0165a0005c0008t0004g0201others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1998-622T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298926 | ||||||
chr2:157298934
|
ACGGAAGA others(1): Show |
A | 261 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(258): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1998-588_1998-581d others(10): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 157298934 | |||||
chr2:157298983
|
C | T | 1 | a0001c0001t0070g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1998-565C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157298983 | ||||||
chr2:157299036
|
G | T | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1998-512G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299036 | ||||||
chr2:157299064
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1998-484G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299064 | ||||||
chr2:157299074
|
C | G | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1998-474C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299074 | ||||||
chr2:157299182
|
G | A | 2 | a0002c0003t0100g0197a0002c0003t0101g0196 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1998-366G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299182 | ||||||
chr2:157299219
|
A | G | 1 | a0008c0013t0032g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1998-329A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299219 | ||||||
chr2:157299285
|
T | A | 32 | a0001c0001t0010g0254a0001c0001t0015g0249a0001c0001t0015g0255others(29): Show | 32 | HG00639.hp1 HG01074.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1998-263T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299285 | ||||||
chr2:157299337
|
T | G | 33 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(30): Show | 34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1998-211T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299337 | ||||||
chr2:157299356
|
A | G | 1 | a0004c0011t0089g0177 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1998-192A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 5/9 | chr2 | 157299356 | ||||||
chr2:157300155
|
T | A | 33 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(30): Show | 34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.2115+490T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300155 | ||||||
chr2:157300205
|
T | C | 1 | a0001c0001t0003g0116 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2116-471T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300205 | ||||||
chr2:157300223
|
G | T | 32 | a0001c0001t0010g0254a0001c0001t0015g0249a0001c0001t0015g0255others(29): Show | 32 | HG00639.hp1 HG01074.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.2116-453G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300223 | ||||||
chr2:157300231
|
G | A | 1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2116-445G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300231 | ||||||
chr2:157300338
|
G | A | 25 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(22): Show | 26 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2116-338G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300338 | ||||||
chr2:157300379
|
A | T | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2116-297A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300379 | ||||||
chr2:157300404
|
A | G | 24 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(21): Show | 25 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2116-272A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300404 | ||||||
chr2:157300405
|
T | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2116-271T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 6/9 | chr2 | 157300405 | ||||||
chr2:157301233
|
G | C | 33 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(30): Show | 34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+234G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301233 | ||||||
chr2:157301282
|
T | C | 28 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(25): Show | 29 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.2439+283T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301282 | ||||||
chr2:157301333
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0007g0029 | 2 | NA18968.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2439+334C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301333 | ||||||
chr2:157301387
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2439+388G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301387 | ||||||
chr2:157301651
|
C | T | 10 | a0001c0001t0073g0087a0001c0001t0088g0246a0002c0003t0007g0209others(7): Show | 10 | HG01261.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2439+652C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301651 | ||||||
chr2:157301753
|
A | C | 1 | a0001c0001t0004g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2439+754A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301753 | ||||||
chr2:157301957
|
A | G | 14 | a0001c0001t0010g0254a0001c0001t0080g0237a0001c0001t0094g0253others(11): Show | 14 | HG00639.hp1 HG01074.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2439+958A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157301957 | ||||||
chr2:157302002
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2439+1003C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302002 | ||||||
chr2:157302128
|
C | T | 3 | a0001c0001t0073g0087a0004c0011t0079g0176a0004c0011t0089g0177 | 3 | HG01891.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2439+1129C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302128 | ||||||
chr2:157302350
|
T | C | 1 | a0002c0003t0004g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2439+1351T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302350 | ||||||
chr2:157302384
|
T | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2439+1385T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302384 | ||||||
chr2:157302460
|
C | A | 1 | a0001c0001t0082g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2439+1461C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302460 | ||||||
chr2:157302582
|
G | GA | 195 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2439+1595dupA | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 157302582 | |||||
chr2:157302925
|
G | C | 59 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(56): Show | 61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.2439+1926G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157302925 | ||||||
chr2:157303009
|
G | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2439+2010G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303009 | ||||||
chr2:157303323
|
C | T | 2 | a0001c0001t0033g0256a0001c0001t0095g0238 | 2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2439+2324C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303323 | ||||||
chr2:157303324
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2439+2325A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303324 | ||||||
chr2:157303340
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2439+2341G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303340 | ||||||
chr2:157303496
|
CTAT | C | 30 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(27): Show | 31 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.2440-2251_2440-224 others(7): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 157303496 | |||||
chr2:157303619
|
GAGATGAT others(4): Show |
G | 2 | a0001c0002t0087g0259a0001c0002t0099g0257 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2440-2128_2440-211 others(15): Show |
GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 157303619 | |||||
chr2:157303633
|
A | G | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2440-2116A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303633 | ||||||
chr2:157303730
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2440-2019A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303730 | ||||||
chr2:157303758
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2440-1991G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303758 | ||||||
chr2:157303794
|
C | A | 2 | a0002c0003t0006g0173a0002c0003t0006g0174 | 2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2440-1955C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303794 | ||||||
chr2:157303800
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2440-1949G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157303800 | ||||||
chr2:157304072
|
G | A | 6 | a0002c0005t0002g0205a0002c0005t0003g0204a0002c0005t0017g0206others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-1677G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304072 | ||||||
chr2:157304390
|
C | A | 1 | a0001c0001t0005g0065 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2440-1359C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304390 | ||||||
chr2:157304511
|
C | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.2440-1238C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304511 | ||||||
chr2:157304519
|
C | G | 90 | a0001c0001t0010g0254a0001c0001t0015g0249a0001c0001t0015g0255others(87): Show | 92 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.2440-1230C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304519 | ||||||
chr2:157304519
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2440-1230C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304519 | ||||||
chr2:157304774
|
A | G | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2440-975A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304774 | ||||||
chr2:157304795
|
T | C | 5 | a0003c0004t0001g0224a0003c0004t0001g0229a0003c0004t0005g0223others(2): Show | 5 | HG00673.hp1 HG02071.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-954T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304795 | ||||||
chr2:157304804
|
A | C | 4 | a0005c0008t0004g0201a0005c0008t0018g0170a0005c0008t0026g0172others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-945A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304804 | ||||||
chr2:157304978
|
A | G | 14 | a0001c0001t0010g0254a0001c0001t0080g0237a0001c0001t0094g0253others(11): Show | 14 | HG00639.hp1 HG01074.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2440-771A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304978 | ||||||
chr2:157304983
|
C | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(268): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.2440-766C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304983 | ||||||
chr2:157304992
|
C | T | 33 | a0001c0002t0010g0252a0001c0002t0034g0093a0001c0002t0047g0092others(30): Show | 34 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.2440-757C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157304992 | ||||||
chr2:157305011
|
G | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2440-738G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305011 | ||||||
chr2:157305023
|
A | G | 1 | a0003c0004t0005g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2440-726A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305023 | ||||||
chr2:157305098
|
T | C | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2440-651T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305098 | ||||||
chr2:157305115
|
G | C | 59 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(56): Show | 61 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.2440-634G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305115 | ||||||
chr2:157305187
|
G | A | 1 | a0001c0002t0008g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2440-562G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305187 | ||||||
chr2:157305225
|
C | A | 2 | a0001c0001t0001g0131a0003c0007t0001g0232 | 2 | HG00621.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.2440-524C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305225 | ||||||
chr2:157305250
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2440-499G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305250 | ||||||
chr2:157305345
|
G | T | 1 | a0002c0003t0004g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2440-404G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305345 | ||||||
chr2:157305521
|
A | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2440-228A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305521 | ||||||
chr2:157305619
|
G | A | 10 | a0001c0001t0073g0087a0001c0001t0088g0246a0002c0003t0007g0209others(7): Show | 10 | HG01261.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2440-130G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305619 | ||||||
chr2:157305650
|
C | A | 2 | a0001c0001t0015g0249a0001c0001t0015g0255 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2440-99C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 7/9 | chr2 | 157305650 | ||||||
chr2:157305963
|
C | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2520+134C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157305963 | ||||||
chr2:157306009
|
T | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2520+180T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306009 | ||||||
chr2:157306106
|
G | T | 2 | a0001c0001t0046g0106a0001c0001t0048g0070 | 2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2520+277G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306106 | ||||||
chr2:157306126
|
C | T | 1 | a0001c0001t0006g0142 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2520+297C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306126 | ||||||
chr2:157306140
|
G | A | 4 | a0001c0002t0047g0092a0001c0002t0066g0096a0001c0002t0096g0239others(1): Show | 4 | HG02970.hp1 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2520+311G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306140 | ||||||
chr2:157306498
|
G | A | 6 | a0001c0002t0002g0006a0001c0002t0002g0030a0001c0002t0002g0078others(3): Show | 7 | HG00741.hp2 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2520+669G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306498 | ||||||
chr2:157306525
|
C | T | 2 | a0001c0001t0004g0103a0001c0001t0006g0048 | 2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2520+696C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306525 | ||||||
chr2:157306914
|
A | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.2520+1085A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157306914 | ||||||
chr2:157307010
|
AT | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2520+1194delT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 157307010 | |||||
chr2:157307106
|
T | C | 1 | a0003c0004t0005g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2520+1277T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307106 | ||||||
chr2:157307155
|
G | A | 26 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(23): Show | 27 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2520+1326G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307155 | ||||||
chr2:157307155
|
G | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.2520+1326G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307155 | ||||||
chr2:157307292
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0138a0001c0001t0004g0139 | 3 | HG03195.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2521-1275G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307292 | ||||||
chr2:157307351
|
C | G | 1 | a0004c0006t0014g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2521-1216C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307351 | ||||||
chr2:157307424
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2521-1143A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307424 | ||||||
chr2:157307597
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2521-970G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307597 | ||||||
chr2:157307624
|
C | T | 1 | a0003c0004t0043g0226 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2521-943C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307624 | ||||||
chr2:157307730
|
T | A | 58 | a0001c0002t0001g0024a0001c0002t0001g0067a0001c0002t0001g0073others(55): Show | 60 | HG00597.hp2 HG00673.hp1 HG01884.hp1 others(57): Show |
intron_variant | MODIFIER | c.2521-837T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307730 | ||||||
chr2:157307733
|
G | A | 1 | a0001c0001t0082g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2521-834G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307733 | ||||||
chr2:157307766
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2521-801C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307766 | ||||||
chr2:157307802
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2521-765G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307802 | ||||||
chr2:157307843
|
C | A | 1 | a0001c0002t0076g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2521-724C>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307843 | ||||||
chr2:157307924
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2521-643C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307924 | ||||||
chr2:157307939
|
G | A | 7 | a0001c0001t0010g0254a0001c0001t0080g0237a0002c0003t0006g0173others(4): Show | 7 | HG00639.hp1 HG01074.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.2521-628G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307939 | ||||||
chr2:157307964
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2521-603A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157307964 | ||||||
chr2:157308012
|
T | C | 2 | a0002c0003t0100g0197a0002c0003t0101g0196 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2521-555T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308012 | ||||||
chr2:157308228
|
A | G | 2 | a0001c0001t0007g0005a0001c0001t0057g0005 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2521-339A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308228 | ||||||
chr2:157308347
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2521-220T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308347 | ||||||
chr2:157308373
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2521-194A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308373 | ||||||
chr2:157308492
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(177): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2521-75C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 8/9 | chr2 | 157308492 | ||||||
chr2:157308889
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2682+161A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157308889 | ||||||
chr2:157308903
|
C | CT | 227 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(224): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2682+185dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 157308903 | |||||
chr2:157309011
|
C | T | 1 | a0004c0006t0013g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2682+283C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309011 | ||||||
chr2:157309028
|
G | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0050others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.2682+300G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309028 | ||||||
chr2:157309082
|
G | A | 1 | a0004c0006t0013g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2682+354G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309082 | ||||||
chr2:157309306
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2682+578T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309306 | ||||||
chr2:157309441
|
T | A | 76 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0050others(73): Show | 78 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2682+713T>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309441 | ||||||
chr2:157309443
|
G | T | 76 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0050others(73): Show | 78 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.2682+715G>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309443 | ||||||
chr2:157309720
|
G | A | 2 | a0001c0002t0091g0240a0001c0002t0092g0245 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2682+992G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309720 | ||||||
chr2:157309745
|
G | C | 69 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0050others(66): Show | 71 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2682+1017G>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309745 | ||||||
chr2:157309877
|
A | G | 129 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0031others(126): Show | 135 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.2682+1149A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309877 | ||||||
chr2:157309953
|
C | T | 1 | a0001c0001t0059g0049 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2682+1225C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157309953 | ||||||
chr2:157310097
|
A | T | 4 | a0001c0002t0077g0250a0001c0002t0078g0247a0001c0002t0086g0248others(1): Show | 4 | HG03130.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-1111A>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310097 | ||||||
chr2:157310109
|
T | C | 2 | a0001c0002t0096g0239a0001c0002t0098g0244 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2683-1099T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310109 | ||||||
chr2:157310424
|
T | C | 7 | a0001c0001t0004g0139a0002c0003t0004g0164a0002c0003t0004g0192others(4): Show | 7 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2683-784T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310424 | ||||||
chr2:157310426
|
G | A | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0002t0076g0251 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2683-782G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310426 | ||||||
chr2:157310466
|
C | G | 3 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0002t0076g0251 | 3 | HG02622.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2683-742C>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310466 | ||||||
chr2:157310682
|
C | T | 4 | a0001c0002t0078g0247a0001c0002t0086g0248a0002c0003t0026g0166others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-526C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310682 | ||||||
chr2:157310775
|
C | T | 5 | a0002c0003t0017g0193a0002c0003t0041g0195a0002c0003t0042g0189others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2683-433C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310775 | ||||||
chr2:157310792
|
T | G | 20 | a0001c0001t0001g0119a0001c0001t0002g0125a0001c0001t0002g0145others(17): Show | 21 | HG00609.hp2 HG00673.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2683-416T>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310792 | ||||||
chr2:157310846
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2683-362C>T | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310846 | ||||||
chr2:157310875
|
A | C | 1 | a0001c0001t0002g0141 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2683-333A>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157310875 | ||||||
chr2:157311026
|
T | C | 8 | a0001c0001t0001g0064a0001c0001t0001g0091a0001c0001t0001g0105others(5): Show | 8 | HG00621.hp1 HG02165.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2683-182T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311026 | ||||||
chr2:157311082
|
T | C | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0094g0253others(1): Show | 4 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-126T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311082 | ||||||
chr2:157311107
|
A | G | 3 | a0001c0001t0016g0113a0001c0001t0016g0154a0001c0002t0034g0093 | 3 | HG02602.hp1 HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2683-101A>G | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311107 | ||||||
chr2:157311124
|
A | AT | 4 | a0001c0001t0015g0249a0001c0001t0015g0255a0001c0001t0094g0253others(1): Show | 4 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-77dupT | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 157311124 | |||||
chr2:157311131
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2683-77T>C | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311131 | ||||||
chr2:157311136
|
G | A | 1 | a0003c0004t0074g0220 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2683-72G>A | GALNT5 | ENSG00000136542.9 | transcript | ENST00000259056.5 | protein_coding | 9/9 | chr2 | 157311136 |