geneid | 4836 |
---|---|
ensemblid | ENSG00000136448.13 |
hgncid | 7857 |
symbol | NMT1 |
name | N-myristoyltransferase 1 |
refseq_nuc | NM_021079.5 |
refseq_prot | NP_066565.1 |
ensembl_nuc | ENST00000258960.7 |
ensembl_prot | ENSP00000258960.2 |
mane_status | MANE Select |
chr | chr17 |
start | 45061317 |
end | 45109016 |
strand | + |
ver | v1.2 |
region | chr17:45061317-45109016 |
region5000 | chr17:45056317-45114016 |
regionname0 | NMT1_chr17_45061317_45109016 |
regionname5000 | NMT1_chr17_45056317_45114016 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 496 | 386 | 92 | 82 | 148 | 16 | 46 | 108 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1491 | 161 | 39 | 37 | 63 | 7 | 14 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
c0002 | 0/1 | 1491 | 84 | 4 | 21 | 41 | 5 | 12 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
c0003 | 0/0 | 1491 | 71 | 14 | 13 | 35 | 0 | 9 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
c0004 | 0/0 | 1491 | 67 | 35 | 11 | 6 | 4 | 11 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
c0005 | 0/0 | 1491 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3391 | 64 | 2 | 11 | 39 | 4 | 7 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0002 | 0/0 | 3391 | 62 | 13 | 9 | 33 | 0 | 7 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0003 | 0/0 | 3391 | 46 | 29 | 4 | 6 | 2 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0004 | 0/0 | 3391 | 34 | 1 | 1 | 29 | 1 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0005 | 0/0 | 3390 | 30 | 3 | 7 | 17 | 1 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0006 | 1/0 | 3391 | 21 | 0 | 10 | 2 | 3 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0007 | 0/0 | 3390 | 12 | 0 | 3 | 6 | 0 | 3 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0008 | 0/0 | 3391 | 10 | 8 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0009 | 0/0 | 3391 | 8 | 0 | 6 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0010 | 0/0 | 3391 | 8 | 6 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0011 | 0/0 | 3391 | 6 | 6 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0012 | 0/0 | 3391 | 5 | 0 | 5 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0013 | 0/0 | 3391 | 5 | 0 | 3 | 0 | 2 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0014 | 0/0 | 3391 | 5 | 0 | 0 | 0 | 0 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0015 | 0/0 | 3390 | 4 | 1 | 1 | 0 | 0 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0016 | 0/0 | 3391 | 4 | 4 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0017 | 0/0 | 3391 | 4 | 1 | 3 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0018 | 0/0 | 3391 | 3 | 1 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0019 | 0/0 | 3391 | 3 | 0 | 2 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0020 | 0/0 | 3391 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0021 | 0/0 | 3390 | 3 | 0 | 2 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0022 | 0/0 | 3391 | 3 | 1 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0023 | 0/0 | 3391 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0024 | 0/0 | 3391 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0025 | 0/0 | 3391 | 2 | 0 | 0 | 0 | 0 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0026 | 0/0 | 3391 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0027 | 0/0 | 3391 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0028 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0029 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0030 | 0/0 | 3391 | 2 | 1 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0031 | 0/0 | 3391 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0032 | 0/0 | 3391 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0033 | 0/0 | 3391 | 2 | 0 | 0 | 0 | 2 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0034 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0035 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0036 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0037 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0038 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0039 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0040 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0041 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0042 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0043 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0044 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0045 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0046 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0047 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0048 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0049 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0050 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0051 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0052 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0053 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
t0054 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 2 | 0 | 2 | 4 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0005 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1491 | 161 | 39 | 37 | 63 | 7 | 14 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002 | 0/1 | 1491 | 84 | 4 | 21 | 41 | 5 | 12 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003 | 0/0 | 1491 | 71 | 14 | 13 | 35 | 0 | 9 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004 | 0/0 | 1491 | 67 | 35 | 11 | 6 | 4 | 11 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0005 | 0/0 | 1491 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0002 | 0/0 | 4881 | 12 | 11 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0004 | 0/0 | 4881 | 26 | 0 | 0 | 26 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0005 | 0/0 | 4880 | 30 | 3 | 7 | 17 | 1 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0006 | 1/0 | 4881 | 21 | 0 | 10 | 2 | 3 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0007 | 0/0 | 4880 | 12 | 0 | 3 | 6 | 0 | 3 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0008 | 0/0 | 4881 | 10 | 8 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0009 | 0/0 | 4881 | 8 | 0 | 6 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0010 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0013 | 0/0 | 4881 | 5 | 0 | 3 | 0 | 2 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0015 | 0/0 | 4880 | 4 | 1 | 1 | 0 | 0 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0016 | 0/0 | 4881 | 4 | 4 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0021 | 0/0 | 4880 | 3 | 0 | 2 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0023 | 0/0 | 4881 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0027 | 0/0 | 4881 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0028 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0029 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0030 | 0/0 | 4881 | 2 | 1 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0035 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0037 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0039 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0042 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0043 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0045 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0046 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0047 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0048 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0049 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0050 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0051 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0001t0052 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0001 | 0/1 | 4881 | 63 | 2 | 11 | 38 | 4 | 7 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0004 | 0/0 | 4881 | 8 | 1 | 1 | 3 | 1 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0012 | 0/0 | 4881 | 5 | 0 | 5 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0018 | 0/0 | 4881 | 3 | 1 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0024 | 0/0 | 4881 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0025 | 0/0 | 4881 | 2 | 0 | 0 | 0 | 0 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0002t0034 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0002 | 0/0 | 4881 | 47 | 2 | 8 | 30 | 0 | 7 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0010 | 0/0 | 4881 | 6 | 4 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0011 | 0/0 | 4881 | 6 | 6 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0019 | 0/0 | 4881 | 3 | 0 | 2 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0020 | 0/0 | 4881 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0026 | 0/0 | 4881 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0036 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0038 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0040 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0003t0041 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0003 | 0/0 | 4881 | 46 | 29 | 4 | 6 | 2 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0014 | 0/0 | 4881 | 5 | 0 | 0 | 0 | 0 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0017 | 0/0 | 4881 | 4 | 1 | 3 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0022 | 0/0 | 4881 | 3 | 1 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0031 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0032 | 0/0 | 4881 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0033 | 0/0 | 4881 | 2 | 0 | 0 | 0 | 2 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0044 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0053 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0004t0054 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
a0001c0005t0002 | 0/0 | 4881 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | copy fasta | chr17 | 45056317 | 45114016 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0005 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0006g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0007g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0008g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0010g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0013g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0013g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0013g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0015g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0015g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0015g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0016g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0016g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0016g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0021g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0021g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0021g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0023g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0023g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0027g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0028g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0029g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0029g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0030g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0035g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0037g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0039g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0042g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0043g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0045g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0046g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0047g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0048g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0049g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0050g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0051g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0001t0052g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0012g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0012g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0012g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0018g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0018g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0018g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0024g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0024g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0025g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0025g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0002t0034g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0010g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0010g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0019g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0019g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0019g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0020g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0020g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0026g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0026g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0036g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0038g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0040g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0003t0041g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0001 | 0/0 | 6 | 0 | 1 | 0 | 2 | 3 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0014g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0014g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0014g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0014g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0014g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0017g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0017g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0022g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0022g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0022g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0031g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0032g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0033g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0033g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0044g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0053g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0004t0054g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0005t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0005t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
a0001c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0324 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00099 | hp2 | a0001 | c0004 | t0033 | g0242 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0268 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00140 | hp2 | a0001 | c0002 | t0004 | g0233 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0193 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00280 | hp2 | a0001 | c0004 | t0033 | g0241 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0329 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00323 | hp2 | a0001 | c0001 | t0050 | g0301 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00408 | hp2 | a0001 | c0001 | t0005 | g0280 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0260 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00423 | hp2 | a0001 | c0003 | t0002 | g0036 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0181 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00558 | hp1 | a0001 | c0001 | t0045 | g0007 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00558 | hp2 | a0001 | c0002 | t0004 | g0171 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00609 | hp1 | a0001 | c0003 | t0002 | g0040 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0336 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00639 | hp2 | a0001 | c0004 | t0003 | g0001 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00642 | hp1 | a0001 | c0001 | t0015 | g0269 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0323 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00733 | hp1 | a0001 | c0002 | t0012 | g0211 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0335 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00735 | hp1 | a0001 | c0004 | t0022 | g0145 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00735 | hp2 | a0001 | c0001 | t0021 | g0300 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0326 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG00741 | hp2 | a0001 | c0002 | t0024 | g0220 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01069 | hp1 | a0001 | c0004 | t0032 | g0014 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01069 | hp2 | a0001 | c0002 | t0034 | g0210 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01070 | hp1 | a0001 | c0004 | t0017 | g0252 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01070 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01071 | hp1 | a0001 | c0004 | t0017 | g0251 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01071 | hp2 | a0001 | c0004 | t0032 | g0014 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01074 | hp2 | a0001 | c0002 | t0012 | g0199 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01081 | hp1 | a0001 | c0004 | t0003 | g0247 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01081 | hp2 | a0001 | c0002 | t0012 | g0206 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01099 | hp1 | a0001 | c0004 | t0022 | g0144 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01099 | hp2 | a0001 | c0002 | t0012 | g0205 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01109 | hp1 | a0001 | c0001 | t0035 | g0004 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01109 | hp2 | a0001 | c0003 | t0010 | g0094 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01167 | hp1 | a0001 | c0004 | t0003 | g0016 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0291 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01168 | hp1 | a0001 | c0002 | t0012 | g0090 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0327 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0337 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0297 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01175 | hp1 | a0001 | c0003 | t0038 | g0096 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01192 | hp1 | a0001 | c0003 | t0019 | g0055 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0333 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01243 | hp2 | a0001 | c0002 | t0018 | g0204 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01255 | hp2 | a0001 | c0004 | t0003 | g0015 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01256 | hp2 | a0001 | c0001 | t0009 | g0131 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0272 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0270 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01261 | hp2 | a0001 | c0003 | t0040 | g0353 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0051 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0298 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01358 | hp1 | a0001 | c0001 | t0009 | g0130 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0339 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01361 | hp1 | a0001 | c0001 | t0021 | g0302 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01361 | hp2 | a0001 | c0002 | t0004 | g0231 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01433 | hp1 | a0001 | c0002 | t0024 | g0164 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0262 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01496 | hp1 | a0001 | c0001 | t0030 | g0331 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01496 | hp2 | a0001 | c0001 | t0009 | g0117 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0218 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01515 | hp2 | a0001 | c0004 | t0003 | g0001 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0060 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0223 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01517 | hp1 | a0001 | c0001 | t0013 | g0061 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01517 | hp2 | a0001 | c0004 | t0003 | g0001 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0354 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01891 | hp1 | a0001 | c0003 | t0011 | g0149 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01891 | hp2 | a0001 | c0001 | t0037 | g0313 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0120 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01934 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01934 | hp2 | a0001 | c0003 | t0002 | g0035 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0325 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01952 | hp1 | a0001 | c0001 | t0006 | g0334 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0338 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01975 | hp2 | a0001 | c0003 | t0002 | g0034 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01978 | hp1 | a0001 | c0001 | t0013 | g0318 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0031 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01993 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01993 | hp2 | a0001 | c0004 | t0017 | g0001 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0009 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02015 | hp1 | a0001 | c0004 | t0003 | g0237 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02027 | hp2 | a0001 | c0003 | t0002 | g0038 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02055 | hp2 | a0001 | c0004 | t0053 | g0070 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02071 | hp1 | a0001 | c0003 | t0002 | g0095 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02074 | hp1 | a0001 | c0003 | t0002 | g0127 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02080 | hp2 | a0001 | c0003 | t0002 | g0041 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02129 | hp1 | a0001 | c0004 | t0003 | g0248 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02135 | hp1 | a0001 | c0001 | t0043 | g0347 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02145 | hp2 | a0001 | c0004 | t0003 | g0348 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02155 | hp1 | a0001 | c0003 | t0002 | g0101 | EAS | CDX | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | CDX | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02257 | hp1 | a0001 | c0002 | t0004 | g0183 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02257 | hp2 | a0001 | c0004 | t0003 | g0214 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02258 | hp1 | a0001 | c0004 | t0003 | g0132 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02258 | hp2 | a0001 | c0001 | t0042 | g0018 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02273 | hp1 | a0001 | c0001 | t0013 | g0343 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02280 | hp1 | a0001 | c0004 | t0003 | g0159 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0342 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0320 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02300 | hp2 | a0001 | c0001 | t0009 | g0009 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02451 | hp2 | a0001 | c0001 | t0028 | g0188 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02602 | hp2 | a0001 | c0004 | t0003 | g0016 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0295 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02622 | hp1 | a0001 | c0003 | t0011 | g0150 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02622 | hp2 | a0001 | c0004 | t0031 | g0012 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02630 | hp1 | a0001 | c0001 | t0016 | g0292 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02630 | hp2 | a0001 | c0004 | t0031 | g0012 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0010 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0293 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02683 | hp1 | a0001 | c0003 | t0002 | g0068 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02683 | hp2 | a0001 | c0004 | t0014 | g0240 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02698 | hp1 | a0001 | c0001 | t0052 | g0341 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0267 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02717 | hp1 | a0001 | c0003 | t0011 | g0161 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02717 | hp2 | a0001 | c0004 | t0003 | g0133 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02723 | hp1 | a0001 | c0001 | t0039 | g0314 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02723 | hp2 | a0001 | c0004 | t0003 | g0158 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0263 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02738 | hp1 | a0001 | c0002 | t0025 | g0081 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0346 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02809 | hp1 | a0001 | c0001 | t0016 | g0294 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02818 | hp1 | a0001 | c0004 | t0054 | g0137 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02886 | hp1 | a0001 | c0004 | t0003 | g0156 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02886 | hp2 | a0001 | c0003 | t0010 | g0186 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02896 | hp1 | a0001 | c0001 | t0048 | g0192 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02896 | hp2 | a0001 | c0004 | t0003 | g0011 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02922 | hp1 | a0001 | c0003 | t0041 | g0053 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02922 | hp2 | a0001 | c0003 | t0011 | g0148 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02970 | hp1 | a0001 | c0004 | t0003 | g0141 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02970 | hp2 | a0001 | c0004 | t0003 | g0350 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02976 | hp1 | a0001 | c0004 | t0003 | g0238 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03017 | hp1 | a0001 | c0002 | t0018 | g0212 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0330 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03041 | hp2 | a0001 | c0004 | t0003 | g0135 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03098 | hp2 | a0001 | c0001 | t0028 | g0187 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03130 | hp1 | a0001 | c0001 | t0049 | g0303 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03130 | hp2 | a0001 | c0004 | t0003 | g0139 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03139 | hp2 | a0001 | c0004 | t0017 | g0146 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0154 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03195 | hp2 | a0001 | c0004 | t0003 | g0138 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03209 | hp1 | a0001 | c0004 | t0003 | g0349 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03209 | hp2 | a0001 | c0001 | t0029 | g0256 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03225 | hp1 | a0001 | c0004 | t0003 | g0160 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03225 | hp2 | a0001 | c0004 | t0003 | g0013 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03239 | hp1 | a0001 | c0004 | t0014 | g0250 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03239 | hp2 | a0001 | c0001 | t0021 | g0299 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0258 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03453 | hp2 | a0001 | c0001 | t0029 | g0255 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03486 | hp1 | a0001 | c0003 | t0011 | g0151 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03486 | hp2 | a0001 | c0004 | t0003 | g0157 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03490 | hp2 | a0001 | c0001 | t0015 | g0284 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03491 | hp1 | a0001 | c0004 | t0003 | g0001 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03491 | hp2 | a0001 | c0001 | t0007 | g0316 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03492 | hp1 | a0001 | c0001 | t0015 | g0279 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03492 | hp2 | a0001 | c0004 | t0003 | g0001 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03540 | hp1 | a0001 | c0004 | t0003 | g0134 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03540 | hp2 | a0001 | c0003 | t0010 | g0189 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03579 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03654 | hp1 | a0001 | c0004 | t0014 | g0312 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0044 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0332 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03688 | hp1 | a0001 | c0004 | t0044 | g0001 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03704 | hp1 | a0001 | c0003 | t0019 | g0062 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0344 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03710 | hp2 | a0001 | c0004 | t0003 | g0015 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03831 | hp1 | a0001 | c0003 | t0002 | g0105 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0319 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03834 | hp1 | a0001 | c0003 | t0010 | g0026 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03834 | hp2 | a0001 | c0002 | t0004 | g0232 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03927 | hp1 | a0001 | c0004 | t0003 | g0001 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03927 | hp2 | a0001 | c0003 | t0002 | g0058 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03942 | hp1 | a0001 | c0004 | t0014 | g0142 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0345 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0045 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG04204 | hp1 | a0001 | c0002 | t0004 | g0184 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG04204 | hp2 | a0001 | c0003 | t0002 | g0059 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0039 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG04228 | hp2 | a0001 | c0004 | t0014 | g0249 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18522 | hp1 | a0001 | c0004 | t0003 | g0010 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0289 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18747 | hp1 | a0001 | c0001 | t0051 | g0328 | EAS | CHB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18747 | hp2 | a0001 | c0001 | t0007 | g0322 | EAS | CHB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0290 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18940 | hp2 | a0001 | c0004 | t0003 | g0246 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18941 | hp2 | a0001 | c0005 | t0002 | g0282 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18942 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18943 | hp2 | a0001 | c0002 | t0004 | g0194 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18945 | hp2 | a0001 | c0001 | t0027 | g0019 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18946 | hp1 | a0001 | c0003 | t0002 | g0225 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18948 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18950 | hp2 | a0001 | c0003 | t0002 | g0032 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18951 | hp1 | a0001 | c0005 | t0002 | g0283 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18953 | hp1 | a0001 | c0003 | t0020 | g0104 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18960 | hp1 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18962 | hp1 | a0001 | c0004 | t0003 | g0244 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18963 | hp2 | a0001 | c0003 | t0002 | g0099 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18964 | hp2 | a0001 | c0005 | t0002 | g0021 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18965 | hp1 | a0001 | c0001 | t0027 | g0019 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18966 | hp2 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18971 | hp1 | a0001 | c0001 | t0009 | g0121 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0042 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18972 | hp2 | a0001 | c0001 | t0006 | g0317 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18973 | hp1 | a0001 | c0004 | t0003 | g0245 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18973 | hp2 | a0001 | c0003 | t0026 | g0056 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18975 | hp2 | a0001 | c0001 | t0046 | g0286 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18978 | hp1 | a0001 | c0003 | t0002 | g0102 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18978 | hp2 | a0001 | c0001 | t0009 | g0125 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18980 | hp1 | a0001 | c0001 | t0007 | g0351 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18991 | hp1 | a0001 | c0001 | t0047 | g0235 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18992 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18994 | hp2 | a0001 | c0001 | t0006 | g0340 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19002 | hp2 | a0001 | c0003 | t0020 | g0097 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19004 | hp1 | a0001 | c0003 | t0026 | g0057 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19004 | hp2 | a0001 | c0003 | t0020 | g0098 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19030 | hp1 | a0001 | c0003 | t0010 | g0191 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0257 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19043 | hp1 | a0001 | c0003 | t0036 | g0075 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19043 | hp2 | a0001 | c0002 | t0018 | g0224 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19056 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19060 | hp1 | a0001 | c0001 | t0023 | g0123 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19064 | hp1 | a0001 | c0003 | t0002 | g0027 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19067 | hp2 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19070 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19074 | hp2 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0352 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19077 | hp2 | a0001 | c0004 | t0003 | g0243 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19087 | hp1 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19088 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19090 | hp2 | a0001 | c0001 | t0023 | g0122 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19240 | hp1 | a0001 | c0003 | t0011 | g0152 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20129 | hp1 | a0001 | c0003 | t0002 | g0030 | AFR | ASW | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20129 | hp2 | a0001 | c0004 | t0003 | g0296 | AFR | ASW | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0217 | EUR | TSI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0203 | EUR | TSI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20905 | hp1 | a0001 | c0002 | t0025 | g0180 | SAS | GIH | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0321 | SAS | GIH | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01123 | hp1 | a0001 | c0003 | t0019 | g0063 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0266 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02109 | hp1 | a0001 | c0004 | t0003 | g0239 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0253 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02486 | hp1 | a0001 | c0004 | t0022 | g0143 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02486 | hp2 | a0001 | c0004 | t0003 | g0136 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02559 | hp1 | a0001 | c0004 | t0003 | g0140 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG02559 | hp2 | a0001 | c0001 | t0030 | g0153 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03471 | hp1 | a0001 | c0003 | t0010 | g0190 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG03471 | hp2 | a0001 | c0004 | t0003 | g0155 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0287 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA20300 | hp2 | a0001 | c0004 | t0003 | g0013 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA21309 | hp1 | a0001 | c0001 | t0010 | g0315 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0089 | REF | REF | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0124 | REF | REF | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45081713
|
A | G | 1 | a0001c0005 | 3 | NA18941.hp2 NA18951.hp1 NA18964.hp2 |
synonymous_variant | LOW | c.201A>G | p.Lys67Lys | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/12 | 214/4881 | 201/1491 | 67/496 | chr17 | 45081713 | ||
chr17:45093786
|
C | T | 1 | a0001c0004 | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
synonymous_variant | LOW | c.487C>T | p.Leu163Leu | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/12 | 500/4881 | 487/1491 | 163/496 | chr17 | 45093786 | ||
chr17:45098538
|
C | T | 2 | a0001c0003a0001c0005 | 74 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(71): Show |
synonymous_variant | LOW | c.870C>T | p.Pro290Pro | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/12 | 883/4881 | 870/1491 | 290/496 | chr17 | 45098538 | ||
chr17:45099436
|
C | T | 1 | a0001c0002 | 84 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
synonymous_variant | LOW | c.916C>T | p.Leu306Leu | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/12 | 929/4881 | 916/1491 | 306/496 | chr17 | 45099436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45105660
|
G | A | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(25): Show | 213 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 21 | chr17 | 45105660 | |||||
chr17:45105681
|
G | A | 1 | a0001c0001t0043 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*42G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 42 | chr17 | 45105681 | |||||
chr17:45105727
|
C | T | 1 | a0001c0001t0042 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 88 | chr17 | 45105727 | |||||
chr17:45105728
|
G | A | 1 | a0001c0001t0027 | 2 | NA18945.hp2 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 89 | chr17 | 45105728 | |||||
chr17:45105730
|
G | A | 1 | a0001c0004t0044 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 91 | chr17 | 45105730 | |||||
chr17:45105740
|
G | A | 12 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(9): Show | 122 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*101G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 101 | chr17 | 45105740 | |||||
chr17:45105832
|
G | A | 1 | a0001c0003t0026 | 2 | NA18973.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 193 | chr17 | 45105832 | |||||
chr17:45105836
|
G | A | 1 | a0001c0002t0034 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 197 | chr17 | 45105836 | |||||
chr17:45106035
|
T | C | 1 | a0001c0003t0019 | 3 | HG01123.hp1 HG01192.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*396T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 396 | chr17 | 45106035 | |||||
chr17:45106052
|
C | T | 10 | a0001c0004t0003a0001c0004t0014a0001c0004t0017others(7): Show | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 413 | chr17 | 45106052 | |||||
chr17:45106294
|
G | A | 2 | a0001c0001t0007a0001c0001t0045 | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*655G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 655 | chr17 | 45106294 | |||||
chr17:45106486
|
G | C | 1 | a0001c0001t0035 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 847 | chr17 | 45106486 | |||||
chr17:45106517
|
G | C | 1 | a0001c0003t0036 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*878G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 878 | chr17 | 45106517 | |||||
chr17:45106577
|
A | G | 1 | a0001c0004t0054 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 938 | chr17 | 45106577 | |||||
chr17:45106784
|
G | T | 1 | a0001c0003t0041 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 1145 | chr17 | 45106784 | |||||
chr17:45107004
|
G | A | 1 | a0001c0001t0028 | 2 | HG02451.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1365G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 1365 | chr17 | 45107004 | |||||
chr17:45107259
|
A | G | 1 | a0001c0004t0033 | 2 | HG00099.hp2 HG00280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1620A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 1620 | chr17 | 45107259 | |||||
chr17:45107655
|
C | A | 4 | a0001c0001t0005a0001c0001t0015a0001c0001t0046others(1): Show | 36 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2016C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2016 | chr17 | 45107655 | |||||
chr17:45107874
|
G | C | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2235G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2235 | chr17 | 45107874 | |||||
chr17:45107930
|
G | C | 6 | a0001c0001t0008a0001c0001t0016a0001c0001t0029others(3): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2291G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2291 | chr17 | 45107930 | |||||
chr17:45107931
|
GT | G | 7 | a0001c0001t0005a0001c0001t0007a0001c0001t0015others(4): Show | 52 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2295delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2295 | INFO_REALIGN_3_PRIME | chr17 | 45107931 | ||||
chr17:45108000
|
C | G | 5 | a0001c0001t0008a0001c0001t0016a0001c0001t0029others(2): Show | 18 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2361 | chr17 | 45108000 | |||||
chr17:45108124
|
C | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | 225 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2485C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2485 | chr17 | 45108124 | |||||
chr17:45108132
|
G | A | 16 | a0001c0001t0010a0001c0001t0016a0001c0001t0037others(13): Show | 81 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2493G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2493 | chr17 | 45108132 | |||||
chr17:45108132
|
G | C | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | 222 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*2493G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2493 | chr17 | 45108132 | |||||
chr17:45108191
|
C | A | 1 | a0001c0001t0049 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2552 | chr17 | 45108191 | |||||
chr17:45108313
|
C | T | 1 | a0001c0001t0028 | 2 | HG02451.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2674C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2674 | chr17 | 45108313 | |||||
chr17:45108314
|
G | A | 1 | a0001c0002t0025 | 2 | HG02738.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2675G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2675 | chr17 | 45108314 | |||||
chr17:45108452
|
T | C | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | 277 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*2813T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2813 | chr17 | 45108452 | |||||
chr17:45108527
|
C | T | 3 | a0001c0003t0020a0001c0003t0038a0001c0003t0040 | 5 | HG01175.hp1 HG01261.hp2 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2888C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2888 | chr17 | 45108527 | |||||
chr17:45108744
|
C | T | 1 | a0001c0001t0049 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3105C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 3105 | chr17 | 45108744 | |||||
chr17:45108750
|
C | T | 1 | a0001c0001t0023 | 2 | NA19060.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3111C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 3111 | chr17 | 45108750 | |||||
chr17:45108830
|
C | G | 1 | a0001c0003t0011 | 6 | HG01891.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3191C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 3191 | chr17 | 45108830 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45061492
|
C | T | 1 | a0001c0002t0001g0354 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.131+32C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45061492 | ||||||
chr17:45061644
|
A | G | 1 | a0001c0003t0040g0353 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.131+184A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45061644 | ||||||
chr17:45061855
|
A | G | 1 | a0001c0003t0002g0352 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.131+395A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45061855 | ||||||
chr17:45062182
|
C | T | 1 | a0001c0001t0007g0351 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.131+722C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062182 | ||||||
chr17:45062603
|
C | T | 3 | a0001c0004t0003g0348a0001c0004t0003g0349a0001c0004t0003g0350 | 3 | HG02145.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.131+1143C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062603 | ||||||
chr17:45062732
|
C | T | 42 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(39): Show | 46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+1272C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062732 | ||||||
chr17:45062775
|
A | G | 2 | a0001c0001t0027g0019a0001c0001t0043g0347 | 3 | HG02135.hp1 NA18945.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.131+1315A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062775 | ||||||
chr17:45062867
|
T | G | 5 | a0001c0001t0010g0018a0001c0001t0010g0315a0001c0001t0037g0313others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+1407T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062867 | ||||||
chr17:45062926
|
C | T | 1 | a0001c0004t0014g0312 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.131+1466C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062926 | ||||||
chr17:45062937
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+1477G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062937 | ||||||
chr17:45063061
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.131+1601C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063061 | ||||||
chr17:45063063
|
G | A | 1 | a0001c0001t0007g0316 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.131+1603G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063063 | ||||||
chr17:45063064
|
G | A | 45 | a0001c0001t0013g0060a0001c0001t0013g0061a0001c0002t0001g0048others(42): Show | 48 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.131+1604G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063064 | ||||||
chr17:45063066
|
G | T | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131+1606G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063066 | ||||||
chr17:45063091
|
A | G | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+1631A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063091 | ||||||
chr17:45063170
|
A | G | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+1710A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063170 | ||||||
chr17:45063204
|
C | CA | 14 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(11): Show | 14 | HG02055.hp2 HG02080.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.131+1768dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | |||||
chr17:45063204
|
CA | C | 143 | a0001c0001t0002g0020a0001c0001t0002g0227a0001c0001t0002g0228others(140): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.131+1768delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | |||||
chr17:45063204
|
CAA | C | 75 | a0001c0001t0005g0005a0001c0001t0005g0259a0001c0001t0005g0260others(72): Show | 81 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.131+1767_131+1768d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | |||||
chr17:45063204
|
CAAA | C | 18 | a0001c0001t0005g0298a0001c0001t0007g0316a0001c0001t0008g0017others(15): Show | 19 | HG00323.hp2 HG00735.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.131+1766_131+1768d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | |||||
chr17:45063232
|
C | G | 60 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0003t0011g0148others(57): Show | 71 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+1772C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063232 | ||||||
chr17:45063289
|
T | C | 1 | a0001c0001t0004g0071 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.131+1829T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063289 | ||||||
chr17:45063484
|
T | TTTCTTTG others(70): Show |
2 | a0001c0001t0009g0130a0001c0001t0009g0131 | 2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.131+2039_131+2040i others(79): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063484 | |||||
chr17:45063559
|
G | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131+2099G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063559 | ||||||
chr17:45063627
|
A | G | 43 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(40): Show | 45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+2167A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063627 | ||||||
chr17:45063693
|
C | T | 3 | a0001c0002t0004g0231a0001c0002t0004g0232a0001c0002t0004g0233 | 3 | HG00140.hp2 HG01361.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.131+2233C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063693 | ||||||
chr17:45063759
|
G | C | 1 | a0001c0004t0003g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.131+2299G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063759 | ||||||
chr17:45063783
|
C | G | 42 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(39): Show | 46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+2323C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063783 | ||||||
chr17:45063887
|
C | A | 37 | a0001c0001t0005g0005a0001c0001t0005g0234a0001c0001t0005g0236others(34): Show | 39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.131+2427C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063887 | ||||||
chr17:45063946
|
G | A | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+2486G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063946 | ||||||
chr17:45063974
|
C | T | 146 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(143): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+2514C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063974 | ||||||
chr17:45064215
|
G | A | 43 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(40): Show | 45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+2755G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064215 | ||||||
chr17:45064245
|
T | C | 1 | a0001c0003t0002g0022 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.131+2785T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064245 | ||||||
chr17:45064266
|
C | T | 146 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(143): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+2806C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064266 | ||||||
chr17:45064388
|
A | G | 32 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(29): Show | 33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+2928A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064388 | ||||||
chr17:45064512
|
G | T | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.131+3052G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064512 | ||||||
chr17:45064513
|
A | T | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.131+3053A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064513 | ||||||
chr17:45064583
|
G | A | 1 | a0001c0004t0003g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.131+3123G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064583 | ||||||
chr17:45064598
|
A | G | 213 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(210): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.131+3138A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064598 | ||||||
chr17:45064802
|
G | C | 42 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(39): Show | 46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+3342G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064802 | ||||||
chr17:45064845
|
G | A | 5 | a0001c0001t0004g0065a0001c0001t0004g0071a0001c0001t0004g0072others(2): Show | 5 | HG00597.hp1 NA18963.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+3385G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064845 | ||||||
chr17:45064881
|
G | T | 43 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(40): Show | 45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+3421G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064881 | ||||||
chr17:45065093
|
T | C | 1 | a0001c0003t0010g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131+3633T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065093 | ||||||
chr17:45065296
|
A | G | 10 | a0001c0001t0013g0060a0001c0001t0013g0061a0001c0003t0002g0054others(7): Show | 10 | HG01123.hp1 HG01192.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.131+3836A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065296 | ||||||
chr17:45065358
|
T | A | 1 | a0001c0003t0002g0054 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131+3898T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065358 | ||||||
chr17:45065394
|
C | T | 32 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(29): Show | 33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+3934C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065394 | ||||||
chr17:45065399
|
G | A | 14 | a0001c0004t0003g0133a0001c0004t0003g0134a0001c0004t0003g0135others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.131+3939G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065399 | ||||||
chr17:45065623
|
C | CA | 85 | a0001c0001t0004g0066a0001c0001t0005g0147a0001c0001t0005g0234others(82): Show | 99 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.131+4184dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45065623 | |||||
chr17:45065623
|
C | CAA | 31 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.131+4183_131+4184d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45065623 | |||||
chr17:45065623
|
CA | C | 40 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0002g0229others(37): Show | 43 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.131+4184delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45065623 | |||||
chr17:45065965
|
G | A | 37 | a0001c0001t0005g0005a0001c0001t0005g0234a0001c0001t0005g0236others(34): Show | 39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.131+4505G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065965 | ||||||
chr17:45065973
|
A | G | 2 | a0001c0001t0002g0308a0001c0001t0002g0309 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.131+4513A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065973 | ||||||
chr17:45066052
|
A | G | 16 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0287others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.131+4592A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066052 | ||||||
chr17:45066117
|
G | A | 1 | a0001c0004t0022g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.131+4657G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066117 | ||||||
chr17:45066294
|
A | G | 50 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.131+4834A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066294 | ||||||
chr17:45066386
|
A | G | 1 | a0001c0004t0003g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131+4926A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066386 | ||||||
chr17:45066672
|
T | C | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+5212T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066672 | ||||||
chr17:45066689
|
T | C | 9 | a0001c0001t0013g0060a0001c0001t0013g0061a0001c0003t0002g0058others(6): Show | 9 | HG01123.hp1 HG01192.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.131+5229T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066689 | ||||||
chr17:45066695
|
T | A | 1 | a0001c0002t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.131+5235T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066695 | ||||||
chr17:45066716
|
T | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+5256T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066716 | ||||||
chr17:45066782
|
A | G | 60 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0003t0011g0148others(57): Show | 71 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+5322A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066782 | ||||||
chr17:45066827
|
C | T | 146 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(143): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+5367C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066827 | ||||||
chr17:45066843
|
G | GCTA | 95 | a0001c0001t0005g0185a0001c0001t0006g0193a0001c0001t0015g0253others(92): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.131+5384_131+5386d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45066843 | |||||
chr17:45066850
|
T | C | 213 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(210): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.131+5390T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066850 | ||||||
chr17:45066920
|
A | G | 61 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0001t0049g0303others(58): Show | 72 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.131+5460A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066920 | ||||||
chr17:45066953
|
C | T | 1 | a0001c0002t0018g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.131+5493C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066953 | ||||||
chr17:45067141
|
G | C | 1 | a0001c0003t0036g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.131+5681G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067141 | ||||||
chr17:45067167
|
A | AT | 6 | a0001c0001t0004g0128a0001c0001t0043g0347a0001c0003t0010g0026others(3): Show | 6 | HG02135.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+5722dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45067167 | |||||
chr17:45067199
|
A | G | 1 | a0001c0001t0005g0285 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.131+5739A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067199 | ||||||
chr17:45067250
|
G | A | 1 | a0001c0003t0010g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131+5790G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067250 | ||||||
chr17:45067445
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+5985T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067445 | ||||||
chr17:45068433
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131+6973T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068433 | ||||||
chr17:45068451
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+6991G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068451 | ||||||
chr17:45068612
|
T | G | 33 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0003t0002g0002others(30): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.131+7152T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068612 | ||||||
chr17:45068807
|
C | T | 1 | a0001c0003t0010g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.131+7347C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068807 | ||||||
chr17:45068808
|
G | A | 37 | a0001c0001t0005g0005a0001c0001t0005g0234a0001c0001t0005g0236others(34): Show | 39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.131+7348G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068808 | ||||||
chr17:45068888
|
C | T | 61 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0001t0049g0303others(58): Show | 72 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.131+7428C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068888 | ||||||
chr17:45068982
|
A | G | 1 | a0001c0001t0021g0302 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131+7522A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068982 | ||||||
chr17:45069064
|
G | A | 95 | a0001c0001t0005g0185a0001c0001t0006g0193a0001c0001t0015g0253others(92): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.131+7604G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069064 | ||||||
chr17:45069108
|
C | G | 9 | a0001c0002t0001g0093a0001c0002t0001g0217a0001c0002t0001g0218others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.131+7648C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069108 | ||||||
chr17:45069238
|
C | T | 2 | a0001c0002t0001g0215a0001c0002t0001g0216 | 2 | NA18942.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.131+7778C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069238 | ||||||
chr17:45069269
|
TTTTATTA others(4): Show |
T | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+7816_131+7826d others(13): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069269 | |||||
chr17:45069273
|
A | AT | 5 | a0001c0001t0010g0018a0001c0001t0010g0315a0001c0001t0037g0313others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+7815dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
A | ATTAT | 6 | a0001c0001t0002g0310a0001c0001t0004g0071a0001c0004t0014g0240others(3): Show | 6 | HG00597.hp1 HG00735.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+7844_131+7847d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
A | ATTATTTA others(1): Show |
41 | a0001c0001t0021g0299a0001c0001t0021g0300a0001c0001t0021g0302others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.131+7840_131+7847d others(10): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
A | ATTATTTA others(5): Show |
38 | a0001c0001t0005g0005a0001c0001t0005g0234a0001c0001t0005g0236others(35): Show | 40 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.131+7836_131+7847d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
A | ATTATTTA others(9): Show |
4 | a0001c0001t0005g0261a0001c0001t0005g0262a0001c0001t0005g0263others(1): Show | 4 | HG01346.hp2 HG01433.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+7832_131+7847d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
A | ATTTAT | 24 | a0001c0001t0006g0317a0001c0001t0006g0327a0001c0001t0006g0329others(21): Show | 25 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.131+7815_131+7816i others(7): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
A | ATTTATTT others(2): Show |
3 | a0001c0001t0006g0324a0001c0001t0006g0325a0001c0001t0006g0326 | 3 | HG00099.hp1 HG00741.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.131+7815_131+7816i others(11): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069273
|
ATTATTTA others(5): Show |
A | 1 | a0001c0004t0003g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.131+7836_131+7847d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | |||||
chr17:45069322
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.131+7862C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069322 | ||||||
chr17:45069360
|
T | G | 1 | a0001c0002t0001g0076 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.131+7900T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069360 | ||||||
chr17:45069362
|
G | C | 43 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(40): Show | 45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+7902G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069362 | ||||||
chr17:45069362
|
G | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+7902G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069362 | ||||||
chr17:45069519
|
C | G | 14 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0287others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.131+8059C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069519 | ||||||
chr17:45069649
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8189C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069649 | ||||||
chr17:45069652
|
C | A | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8192C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069652 | ||||||
chr17:45069654
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8194C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069654 | ||||||
chr17:45069839
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8379C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069839 | ||||||
chr17:45069879
|
C | CA | 38 | a0001c0001t0015g0253a0001c0001t0047g0235a0001c0002t0001g0077others(35): Show | 38 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.131+8435dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069879 | |||||
chr17:45069879
|
CA | C | 12 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(9): Show | 12 | HG00735.hp1 HG01169.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.131+8435delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069879 | |||||
chr17:45069907
|
A | G | 146 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(143): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+8447A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069907 | ||||||
chr17:45069976
|
G | T | 1 | a0001c0002t0001g0085 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.131+8516G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069976 | ||||||
chr17:45069983
|
C | T | 42 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(39): Show | 46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+8523C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069983 | ||||||
chr17:45070071
|
A | C | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+8611A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070071 | ||||||
chr17:45070083
|
C | T | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+8623C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070083 | ||||||
chr17:45070175
|
G | C | 5 | a0001c0001t0010g0018a0001c0001t0010g0315a0001c0001t0037g0313others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+8715G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070175 | ||||||
chr17:45070186
|
A | G | 32 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(29): Show | 33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+8726A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070186 | ||||||
chr17:45070214
|
A | G | 61 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0001t0049g0303others(58): Show | 72 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.131+8754A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070214 | ||||||
chr17:45070255
|
T | G | 1 | a0001c0004t0022g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.131+8795T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070255 | ||||||
chr17:45070255
|
T | TTG | 32 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(29): Show | 33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+8810_131+8811d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45070255 | |||||
chr17:45070399
|
C | T | 1 | a0001c0001t0050g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.131+8939C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070399 | ||||||
chr17:45070401
|
C | T | 2 | a0001c0001t0009g0130a0001c0001t0009g0131 | 2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.131+8941C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070401 | ||||||
chr17:45070540
|
C | T | 2 | a0001c0003t0002g0050a0001c0005t0002g0021 | 2 | NA18964.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.131+9080C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070540 | ||||||
chr17:45070597
|
T | C | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+9137T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070597 | ||||||
chr17:45070657
|
T | TTA | 57 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0003t0011g0148others(54): Show | 68 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.131+9197_131+9198i others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070657 | ||||||
chr17:45070659
|
C | T | 50 | a0001c0001t0002g0129a0001c0001t0002g0228a0001c0001t0002g0229others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.131+9199C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070659 | ||||||
chr17:45070798
|
C | T | 60 | a0001c0001t0005g0147a0001c0001t0030g0153a0001c0001t0049g0303others(57): Show | 71 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+9338C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070798 | ||||||
chr17:45070839
|
A | G | 1 | a0001c0002t0001g0213 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.131+9379A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070839 | ||||||
chr17:45070912
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+9452A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070912 | ||||||
chr17:45070948
|
C | T | 1 | a0001c0003t0002g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.131+9488C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070948 | ||||||
chr17:45071106
|
C | T | 1 | a0001c0003t0010g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131+9646C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071106 | ||||||
chr17:45071142
|
G | A | 34 | a0001c0001t0005g0005a0001c0001t0005g0234a0001c0001t0005g0236others(31): Show | 36 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.131+9682G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071142 | ||||||
chr17:45071258
|
A | C | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+9798A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071258 | ||||||
chr17:45071276
|
C | G | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+9816C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071276 | ||||||
chr17:45071318
|
C | T | 2 | a0001c0004t0003g0133a0001c0004t0054g0137 | 2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.131+9858C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071318 | ||||||
chr17:45071389
|
G | C | 1 | a0001c0003t0019g0055 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.131+9929G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071389 | ||||||
chr17:45071848
|
C | T | 3 | a0001c0003t0019g0055a0001c0003t0019g0062a0001c0003t0019g0063 | 3 | HG01123.hp1 HG01192.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.132-9796C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071848 | ||||||
chr17:45071867
|
G | A | 34 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0234others(31): Show | 36 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.132-9777G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071867 | ||||||
chr17:45072066
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.132-9578A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072066 | ||||||
chr17:45072252
|
T | TA | 37 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(34): Show | 39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.132-9391dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45072252 | |||||
chr17:45072254
|
C | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-9390C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072254 | ||||||
chr17:45072404
|
C | T | 7 | a0001c0004t0003g0015a0001c0004t0003g0016a0001c0004t0014g0240others(4): Show | 9 | HG01070.hp1 HG01071.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.132-9240C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072404 | ||||||
chr17:45072608
|
G | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-9036G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072608 | ||||||
chr17:45072620
|
T | C | 241 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(238): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-9024T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072620 | ||||||
chr17:45072672
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.132-8972G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072672 | ||||||
chr17:45072680
|
C | G | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-8964C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072680 | ||||||
chr17:45072684
|
C | T | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-8960C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072684 | ||||||
chr17:45072734
|
C | T | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.132-8910C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072734 | ||||||
chr17:45072757
|
C | A | 2 | a0001c0003t0026g0056a0001c0003t0026g0057 | 2 | NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.132-8887C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072757 | ||||||
chr17:45072825
|
C | T | 2 | a0001c0004t0003g0348a0001c0004t0003g0349 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.132-8819C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072825 | ||||||
chr17:45072838
|
C | T | 2 | a0001c0001t0009g0130a0001c0001t0009g0131 | 2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.132-8806C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072838 | ||||||
chr17:45072841
|
G | A | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.132-8803G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072841 | ||||||
chr17:45072848
|
C | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-8796C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072848 | ||||||
chr17:45072849
|
G | A | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-8795G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072849 | ||||||
chr17:45072874
|
A | G | 88 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(85): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-8770A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072874 | ||||||
chr17:45073045
|
G | C | 1 | a0001c0001t0009g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.132-8599G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073045 | ||||||
chr17:45073206
|
G | A | 3 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168 | 3 | NA19062.hp1 NA19068.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.132-8438G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073206 | ||||||
chr17:45073599
|
A | G | 2 | a0001c0003t0026g0056a0001c0003t0026g0057 | 2 | NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.132-8045A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073599 | ||||||
chr17:45073712
|
C | T | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.132-7932C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073712 | ||||||
chr17:45073862
|
G | T | 1 | a0001c0003t0011g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.132-7782G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073862 | ||||||
chr17:45073909
|
T | C | 356 | a0001c0001t0001g0111a0001c0001t0002g0020a0001c0001t0002g0129others(353): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.132-7735T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073909 | ||||||
chr17:45074032
|
T | C | 241 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(238): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-7612T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074032 | ||||||
chr17:45074105
|
G | T | 88 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(85): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-7539G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074105 | ||||||
chr17:45074137
|
G | T | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.132-7507G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074137 | ||||||
chr17:45074217
|
C | CT | 65 | a0001c0001t0004g0069a0001c0001t0005g0005a0001c0001t0005g0147others(62): Show | 71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.132-7412dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45074217 | |||||
chr17:45074217
|
C | CTT | 83 | a0001c0001t0002g0020a0001c0001t0005g0259a0001c0001t0006g0193others(80): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.132-7413_132-7412d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45074217 | |||||
chr17:45074217
|
C | CTTT | 6 | a0001c0001t0006g0326a0001c0001t0006g0344a0001c0001t0013g0318others(3): Show | 6 | HG00741.hp1 HG01978.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-7414_132-7412d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45074217 | |||||
chr17:45074231
|
T | TC | 87 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.132-7413_132-7412i others(3): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074231 | ||||||
chr17:45074242
|
T | C | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-7402T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074242 | ||||||
chr17:45074253
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.132-7391C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074253 | ||||||
chr17:45074289
|
A | G | 1 | a0001c0002t0012g0211 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132-7355A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074289 | ||||||
chr17:45074317
|
C | A | 1 | a0001c0003t0002g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.132-7327C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074317 | ||||||
chr17:45074942
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.132-6702G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074942 | ||||||
chr17:45075053
|
G | A | 1 | a0001c0002t0004g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.132-6591G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075053 | ||||||
chr17:45075142
|
C | G | 1 | a0001c0001t0005g0280 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.132-6502C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075142 | ||||||
chr17:45075146
|
C | T | 1 | a0001c0004t0003g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.132-6498C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075146 | ||||||
chr17:45075222
|
G | A | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-6422G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075222 | ||||||
chr17:45075307
|
A | G | 88 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(85): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-6337A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075307 | ||||||
chr17:45075312
|
C | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-6332C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075312 | ||||||
chr17:45075351
|
C | G | 241 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(238): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-6293C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075351 | ||||||
chr17:45075434
|
G | A | 1 | a0001c0003t0010g0186 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.132-6210G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075434 | ||||||
chr17:45075509
|
T | C | 152 | a0001c0001t0002g0020a0001c0001t0005g0005a0001c0001t0005g0147others(149): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.132-6135T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075509 | ||||||
chr17:45075555
|
G | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0320a0001c0001t0007g0322others(3): Show | 7 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-6089G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075555 | ||||||
chr17:45075573
|
A | C | 2 | a0001c0001t0015g0279a0001c0001t0015g0284 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.132-6071A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075573 | ||||||
chr17:45075580
|
G | A | 1 | a0001c0004t0003g0349 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.132-6064G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075580 | ||||||
chr17:45075596
|
A | G | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-6048A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075596 | ||||||
chr17:45075638
|
A | G | 241 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(238): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-6006A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075638 | ||||||
chr17:45075732
|
T | G | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-5912T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075732 | ||||||
chr17:45075800
|
T | C | 354 | a0001c0001t0001g0111a0001c0001t0002g0020a0001c0001t0002g0129others(351): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.132-5844T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075800 | ||||||
chr17:45075867
|
C | T | 9 | a0001c0002t0001g0093a0001c0002t0001g0217a0001c0002t0001g0218others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.132-5777C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075867 | ||||||
chr17:45075868
|
A | T | 1 | a0001c0001t0052g0341 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.132-5776A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075868 | ||||||
chr17:45075992
|
C | A | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-5652C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075992 | ||||||
chr17:45076021
|
G | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-5623G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076021 | ||||||
chr17:45076196
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.132-5448T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076196 | ||||||
chr17:45076267
|
A | G | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-5377A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076267 | ||||||
chr17:45076344
|
G | T | 3 | a0001c0004t0022g0143a0001c0004t0022g0144a0001c0004t0022g0145 | 3 | HG00735.hp1 HG01099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.132-5300G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076344 | ||||||
chr17:45076402
|
C | T | 1 | a0001c0001t0047g0235 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.132-5242C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076402 | ||||||
chr17:45076451
|
GA | G | 6 | a0001c0001t0008g0287a0001c0001t0029g0255a0001c0001t0029g0256others(3): Show | 6 | HG01069.hp2 HG01361.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-5179delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45076451 | |||||
chr17:45076452
|
A | C | 36 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(33): Show | 38 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.132-5192A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076452 | ||||||
chr17:45076477
|
C | T | 1 | a0001c0001t0009g0121 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.132-5167C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076477 | ||||||
chr17:45076890
|
T | C | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-4754T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076890 | ||||||
chr17:45076912
|
T | C | 1 | a0001c0003t0002g0028 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.132-4732T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076912 | ||||||
chr17:45077004
|
T | C | 14 | a0001c0003t0002g0002a0001c0003t0002g0022a0001c0003t0002g0023others(11): Show | 17 | HG01070.hp2 HG01261.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-4640T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077004 | ||||||
chr17:45077169
|
T | C | 16 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0287others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-4475T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077169 | ||||||
chr17:45077225
|
T | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-4419T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077225 | ||||||
chr17:45077789
|
A | G | 2 | a0001c0004t0003g0138a0001c0004t0003g0139 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.132-3855A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077789 | ||||||
chr17:45077980
|
T | A | 1 | a0001c0002t0001g0085 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.132-3664T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077980 | ||||||
chr17:45078011
|
C | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-3633C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078011 | ||||||
chr17:45078242
|
TG | T | 12 | a0001c0002t0001g0067a0001c0002t0001g0076a0001c0002t0001g0086others(9): Show | 12 | HG00597.hp2 NA18940.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.132-3395delG | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45078242 | |||||
chr17:45078245
|
G | A | 2 | a0001c0004t0033g0241a0001c0004t0033g0242 | 2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.132-3399G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078245 | ||||||
chr17:45078483
|
C | T | 5 | a0001c0002t0004g0183a0001c0002t0004g0184a0001c0002t0004g0231others(2): Show | 5 | HG00140.hp2 HG01361.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-3161C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078483 | ||||||
chr17:45078486
|
G | GTA | 6 | a0001c0001t0005g0278a0001c0001t0010g0018a0001c0001t0010g0315others(3): Show | 6 | HG01891.hp2 HG02132.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-3145_132-3144d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45078486 | |||||
chr17:45078546
|
G | A | 241 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(238): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-3098G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078546 | ||||||
chr17:45078579
|
T | C | 4 | a0001c0001t0005g0259a0001c0001t0005g0266a0001c0001t0005g0267others(1): Show | 4 | HG00140.hp1 HG01123.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.132-3065T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078579 | ||||||
chr17:45078612
|
A | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-3032A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078612 | ||||||
chr17:45078655
|
T | C | 83 | a0001c0002t0001g0008a0001c0002t0001g0048a0001c0002t0001g0049others(80): Show | 84 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.132-2989T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078655 | ||||||
chr17:45078708
|
C | T | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-2936C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078708 | ||||||
chr17:45078767
|
A | T | 82 | a0001c0002t0001g0008a0001c0002t0001g0048a0001c0002t0001g0049others(79): Show | 83 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.132-2877A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078767 | ||||||
chr17:45078836
|
G | A | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-2808G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078836 | ||||||
chr17:45078907
|
C | T | 1 | a0001c0003t0041g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.132-2737C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078907 | ||||||
chr17:45079077
|
T | C | 1 | a0001c0004t0003g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.132-2567T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079077 | ||||||
chr17:45079085
|
T | C | 16 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0287others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-2559T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079085 | ||||||
chr17:45079117
|
T | TC | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-2523dupC | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45079117 | |||||
chr17:45079190
|
A | C | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-2454A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079190 | ||||||
chr17:45079348
|
T | C | 153 | a0001c0001t0002g0020a0001c0001t0005g0005a0001c0001t0005g0147others(150): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.132-2296T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079348 | ||||||
chr17:45079351
|
C | T | 43 | a0001c0004t0003g0001a0001c0004t0003g0010a0001c0004t0003g0011others(40): Show | 55 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.132-2293C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079351 | ||||||
chr17:45079449
|
A | G | 1 | a0001c0001t0010g0315 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132-2195A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079449 | ||||||
chr17:45079450
|
C | T | 9 | a0001c0004t0003g0133a0001c0004t0003g0135a0001c0004t0003g0136others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.132-2194C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079450 | ||||||
chr17:45079478
|
A | G | 1 | a0001c0001t0006g0344 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.132-2166A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079478 | ||||||
chr17:45079494
|
C | G | 1 | a0001c0003t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132-2150C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079494 | ||||||
chr17:45079547
|
T | C | 16 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0287others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-2097T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079547 | ||||||
chr17:45079591
|
C | T | 1 | a0001c0003t0002g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.132-2053C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079591 | ||||||
chr17:45079615
|
A | G | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.132-2029A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079615 | ||||||
chr17:45079724
|
G | A | 88 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(85): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-1920G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079724 | ||||||
chr17:45079756
|
G | A | 1 | a0001c0002t0012g0199 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.132-1888G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079756 | ||||||
chr17:45079840
|
T | C | 4 | a0001c0001t0015g0253a0001c0001t0015g0269a0001c0001t0015g0279others(1): Show | 4 | HG00642.hp1 HG02109.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-1804T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079840 | ||||||
chr17:45079866
|
AT | A | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.132-1772delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45079866 | |||||
chr17:45079890
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.132-1754G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079890 | ||||||
chr17:45079961
|
A | G | 150 | a0001c0001t0002g0020a0001c0001t0005g0005a0001c0001t0005g0147others(147): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.132-1683A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079961 | ||||||
chr17:45080167
|
CT | C | 88 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(85): Show | 91 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.132-1467delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080167 | |||||
chr17:45080279
|
G | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-1365G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080279 | ||||||
chr17:45080288
|
G | C | 32 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(29): Show | 33 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.132-1356G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080288 | ||||||
chr17:45080322
|
G | A | 5 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(2): Show | 6 | HG02451.hp1 HG03516.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-1322G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080322 | ||||||
chr17:45080341
|
G | A | 150 | a0001c0001t0002g0020a0001c0001t0005g0005a0001c0001t0005g0147others(147): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.132-1303G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080341 | ||||||
chr17:45080465
|
C | CT | 23 | a0001c0001t0004g0066a0001c0001t0004g0071a0001c0001t0007g0006others(20): Show | 27 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.132-1158dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080465 | |||||
chr17:45080465
|
CT | C | 204 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(201): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.132-1158delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080465 | |||||
chr17:45080465
|
CTT | C | 76 | a0001c0001t0013g0060a0001c0001t0028g0187a0001c0001t0028g0188others(73): Show | 79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.132-1159_132-1158d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080465 | |||||
chr17:45080534
|
TCTCGGCT others(87): Show |
T | 1 | a0001c0004t0003g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.132-1108_132-1015d others(96): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080534 | |||||
chr17:45080535
|
C | G | 8 | a0001c0001t0028g0187a0001c0001t0028g0188a0001c0003t0010g0094others(5): Show | 8 | HG01109.hp2 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.132-1109C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080535 | ||||||
chr17:45080614
|
G | A | 76 | a0001c0001t0008g0287a0001c0001t0028g0187a0001c0001t0028g0188others(73): Show | 79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.132-1030G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080614 | ||||||
chr17:45080623
|
C | T | 1 | a0001c0004t0031g0012 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.132-1021C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080623 | ||||||
chr17:45080688
|
C | G | 1 | a0001c0003t0002g0035 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.132-956C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080688 | ||||||
chr17:45080847
|
A | G | 1 | a0001c0001t0005g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.132-797A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080847 | ||||||
chr17:45081268
|
T | C | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.132-376T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081268 | ||||||
chr17:45081306
|
G | A | 88 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(85): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-338G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081306 | ||||||
chr17:45081454
|
C | T | 1 | a0001c0003t0019g0063 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.132-190C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081454 | ||||||
chr17:45081534
|
G | A | 32 | a0001c0001t0002g0020a0001c0001t0006g0193a0001c0001t0006g0317others(29): Show | 33 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.132-110G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081534 | ||||||
chr17:45081782
|
C | T | 1 | a0001c0001t0004g0119 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.240+30C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45081782 | ||||||
chr17:45081951
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240+199G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45081951 | ||||||
chr17:45082057
|
G | A | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+305G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082057 | ||||||
chr17:45082091
|
C | T | 5 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0215others(2): Show | 5 | NA18942.hp2 NA18986.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+339C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082091 | ||||||
chr17:45082272
|
G | GT | 7 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(4): Show | 7 | HG02055.hp2 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+535dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45082272 | |||||
chr17:45082375
|
C | G | 9 | a0001c0001t0028g0187a0001c0001t0028g0188a0001c0003t0010g0026others(6): Show | 9 | HG01109.hp2 HG02451.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+623C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082375 | ||||||
chr17:45082465
|
C | T | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(8): Show | 14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+713C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082465 | ||||||
chr17:45082517
|
A | G | 3 | a0001c0003t0010g0094a0001c0003t0010g0190a0001c0003t0010g0191 | 3 | HG01109.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.240+765A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082517 | ||||||
chr17:45082565
|
A | G | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.240+813A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082565 | ||||||
chr17:45082605
|
T | A | 1 | a0001c0004t0003g0134 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.240+853T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082605 | ||||||
chr17:45082705
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.240+953C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082705 | ||||||
chr17:45082786
|
C | T | 1 | a0001c0001t0008g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.240+1034C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082786 | ||||||
chr17:45082788
|
G | T | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1036G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082788 | ||||||
chr17:45082974
|
G | A | 3 | a0001c0001t0008g0287a0001c0001t0029g0255a0001c0001t0029g0256 | 3 | HG03209.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.240+1222G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082974 | ||||||
chr17:45083131
|
A | G | 73 | a0001c0001t0028g0187a0001c0001t0028g0188a0001c0003t0002g0002others(70): Show | 76 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.240+1379A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083131 | ||||||
chr17:45083171
|
T | C | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(8): Show | 14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1419T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083171 | ||||||
chr17:45083180
|
G | T | 82 | a0001c0002t0001g0008a0001c0002t0001g0048a0001c0002t0001g0049others(79): Show | 83 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.240+1428G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083180 | ||||||
chr17:45083182
|
G | C | 1 | a0001c0002t0001g0085 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.240+1430G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083182 | ||||||
chr17:45083190
|
G | A | 76 | a0001c0001t0008g0287a0001c0001t0028g0187a0001c0001t0028g0188others(73): Show | 79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.240+1438G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083190 | ||||||
chr17:45083203
|
C | T | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(8): Show | 14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1451C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083203 | ||||||
chr17:45083271
|
A | G | 1 | a0001c0002t0004g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.240+1519A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083271 | ||||||
chr17:45083297
|
C | T | 1 | a0001c0003t0011g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.240+1545C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083297 | ||||||
chr17:45083318
|
C | CA | 12 | a0001c0001t0002g0310a0001c0001t0006g0326a0001c0001t0043g0347others(9): Show | 12 | HG00423.hp2 HG00741.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+1581dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45083318 | |||||
chr17:45083334
|
T | A | 1 | a0001c0002t0001g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.240+1582T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083334 | ||||||
chr17:45083335
|
TA | T | 81 | a0001c0002t0001g0008a0001c0002t0001g0048a0001c0002t0001g0049others(78): Show | 82 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.240+1592delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45083335 | |||||
chr17:45083336
|
A | T | 40 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(37): Show | 42 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.240+1584A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083336 | ||||||
chr17:45083360
|
A | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.240+1608A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083360 | ||||||
chr17:45083395
|
C | G | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(8): Show | 14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1643C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083395 | ||||||
chr17:45083442
|
A | G | 3 | a0001c0003t0010g0094a0001c0003t0010g0190a0001c0003t0010g0191 | 3 | HG01109.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.240+1690A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083442 | ||||||
chr17:45083468
|
A | G | 5 | a0001c0001t0010g0018a0001c0001t0010g0315a0001c0001t0037g0313others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1716A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083468 | ||||||
chr17:45083471
|
G | A | 3 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272 | 3 | HG01074.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.240+1719G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083471 | ||||||
chr17:45083647
|
C | G | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.240+1895C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083647 | ||||||
chr17:45083737
|
C | T | 86 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(83): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.240+1985C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083737 | ||||||
chr17:45083746
|
A | G | 150 | a0001c0001t0002g0310a0001c0001t0005g0005a0001c0001t0005g0147others(147): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.240+1994A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083746 | ||||||
chr17:45083787
|
A | G | 2 | a0001c0001t0005g0264a0001c0001t0005g0265 | 2 | NA19002.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.240+2035A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083787 | ||||||
chr17:45083807
|
C | A | 1 | a0001c0002t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.240+2055C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083807 | ||||||
chr17:45083952
|
T | C | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(8): Show | 14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+2200T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083952 | ||||||
chr17:45083985
|
C | T | 242 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(239): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.240+2233C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083985 | ||||||
chr17:45084046
|
A | G | 1 | a0001c0003t0002g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.240+2294A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084046 | ||||||
chr17:45084336
|
C | CT | 337 | a0001c0001t0001g0111a0001c0001t0002g0129a0001c0001t0002g0227others(334): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.241-2158dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45084336 | |||||
chr17:45084336
|
C | CTT | 20 | a0001c0001t0002g0020a0001c0001t0002g0229a0001c0001t0004g0126others(17): Show | 20 | HG00438.hp1 HG01109.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.241-2159_241-2158d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45084336 | |||||
chr17:45084352
|
C | T | 1 | a0001c0001t0047g0235 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.241-2156C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084352 | ||||||
chr17:45084456
|
T | C | 1 | a0001c0001t0006g0324 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.241-2052T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084456 | ||||||
chr17:45084475
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.241-2033C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084475 | ||||||
chr17:45084483
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.241-2025C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084483 | ||||||
chr17:45084494
|
T | C | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.241-2014T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084494 | ||||||
chr17:45084572
|
A | G | 1 | a0001c0001t0039g0314 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.241-1936A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084572 | ||||||
chr17:45084584
|
C | T | 55 | a0001c0004t0003g0001a0001c0004t0003g0010a0001c0004t0003g0011others(52): Show | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-1924C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084584 | ||||||
chr17:45084622
|
C | T | 73 | a0001c0001t0028g0187a0001c0001t0028g0188a0001c0003t0002g0002others(70): Show | 76 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.241-1886C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084622 | ||||||
chr17:45084641
|
T | C | 4 | a0001c0001t0015g0253a0001c0001t0015g0269a0001c0001t0015g0279others(1): Show | 4 | HG00642.hp1 HG02109.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-1867T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084641 | ||||||
chr17:45084756
|
C | T | 1 | a0001c0002t0004g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.241-1752C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084756 | ||||||
chr17:45084772
|
C | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0320a0001c0001t0007g0322others(3): Show | 7 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-1736C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084772 | ||||||
chr17:45084797
|
A | G | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.241-1711A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084797 | ||||||
chr17:45084899
|
A | G | 1 | a0001c0003t0019g0063 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.241-1609A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084899 | ||||||
chr17:45085017
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.241-1491T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085017 | ||||||
chr17:45085018
|
T | TGGGCACA others(11): Show |
1 | a0001c0002t0001g0166 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.241-1485_241-1484i others(20): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085018 | |||||
chr17:45085027
|
C | G | 1 | a0001c0001t0006g0338 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.241-1481C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085027 | ||||||
chr17:45085408
|
C | G | 87 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(84): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.241-1100C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085408 | ||||||
chr17:45085470
|
T | C | 1 | a0001c0004t0003g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.241-1038T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085470 | ||||||
chr17:45085520
|
T | C | 2 | a0001c0002t0025g0081a0001c0002t0025g0180 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.241-988T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085520 | ||||||
chr17:45085554
|
A | G | 14 | a0001c0003t0002g0054a0001c0003t0002g0058a0001c0003t0002g0059others(11): Show | 14 | HG01123.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.241-954A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085554 | ||||||
chr17:45085589
|
G | GT | 358 | a0001c0001t0001g0111a0001c0001t0002g0020a0001c0001t0002g0129others(355): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.241-918dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085589 | |||||
chr17:45085651
|
T | C | 55 | a0001c0004t0003g0001a0001c0004t0003g0010a0001c0004t0003g0011others(52): Show | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-857T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085651 | ||||||
chr17:45085704
|
G | A | 2 | a0001c0001t0008g0287a0001c0001t0029g0255 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.241-804G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085704 | ||||||
chr17:45085709
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.241-799G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085709 | ||||||
chr17:45085819
|
C | CT | 39 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(36): Show | 41 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.241-676dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085819 | |||||
chr17:45085819
|
C | CTT | 12 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(9): Show | 13 | HG01169.hp2 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-677_241-676dup others(2): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085819 | |||||
chr17:45085819
|
CT | C | 13 | a0001c0001t0006g0327a0001c0001t0007g0006a0001c0001t0007g0007others(10): Show | 16 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.241-676delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085819 | |||||
chr17:45085870
|
G | A | 19 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0079others(16): Show | 19 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.241-638G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085870 | ||||||
chr17:45085957
|
G | C | 93 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(90): Show | 96 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.241-551G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085957 | ||||||
chr17:45085965
|
G | T | 2 | a0001c0004t0003g0160a0001c0004t0031g0012 | 3 | HG02622.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.241-543G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085965 | ||||||
chr17:45085970
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-538C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085970 | ||||||
chr17:45085974
|
G | A | 1 | a0001c0003t0041g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.241-534G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085974 | ||||||
chr17:45085987
|
A | T | 2 | a0001c0001t0009g0130a0001c0001t0009g0131 | 2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.241-521A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085987 | ||||||
chr17:45086124
|
C | CT | 12 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(9): Show | 12 | HG00735.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-367dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45086124 | |||||
chr17:45086124
|
C | CTTT | 28 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(25): Show | 30 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.241-369_241-367dup others(3): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45086124 | |||||
chr17:45086124
|
C | CTTTT | 10 | a0001c0001t0005g0259a0001c0001t0005g0262a0001c0001t0005g0263others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-370_241-367dup others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45086124 | |||||
chr17:45086185
|
G | A | 2 | a0001c0004t0022g0144a0001c0004t0022g0145 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.241-323G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086185 | ||||||
chr17:45086322
|
A | G | 1 | a0001c0001t0006g0326 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241-186A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086322 | ||||||
chr17:45086325
|
A | T | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-183A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086325 | ||||||
chr17:45086373
|
C | T | 1 | a0001c0004t0003g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.241-135C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086373 | ||||||
chr17:45086385
|
A | G | 1 | a0001c0003t0010g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241-123A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086385 | ||||||
chr17:45086388
|
A | G | 242 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(239): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.241-120A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086388 | ||||||
chr17:45086483
|
T | C | 152 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(149): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.241-25T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086483 | ||||||
chr17:45086799
|
A | T | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+147A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45086799 | ||||||
chr17:45086878
|
G | T | 86 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(83): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.385+226G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45086878 | ||||||
chr17:45086998
|
T | TA | 154 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(151): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.385+360dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45086998 | |||||
chr17:45087187
|
CA | C | 5 | a0001c0002t0012g0090a0001c0002t0012g0199a0001c0002t0012g0205others(2): Show | 5 | HG00733.hp1 HG01074.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+545delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45087187 | |||||
chr17:45087774
|
G | A | 1 | a0001c0001t0006g0326 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.385+1122G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087774 | ||||||
chr17:45087774
|
G | C | 15 | a0001c0003t0002g0054a0001c0003t0002g0058a0001c0003t0002g0059others(12): Show | 15 | HG01123.hp1 HG01192.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.385+1122G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087774 | ||||||
chr17:45087817
|
T | C | 152 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(149): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.385+1165T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087817 | ||||||
chr17:45087891
|
C | A | 1 | a0001c0001t0005g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.385+1239C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087891 | ||||||
chr17:45088016
|
T | A | 86 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(83): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.385+1364T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088016 | ||||||
chr17:45088180
|
G | A | 7 | a0001c0004t0003g0133a0001c0004t0003g0135a0001c0004t0003g0136others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+1528G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088180 | ||||||
chr17:45088470
|
T | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+1818T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088470 | ||||||
chr17:45088519
|
T | C | 152 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(149): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.385+1867T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088519 | ||||||
chr17:45088556
|
A | G | 2 | a0001c0001t0005g0264a0001c0001t0005g0265 | 2 | NA19002.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.385+1904A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088556 | ||||||
chr17:45088584
|
G | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+1932G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088584 | ||||||
chr17:45088689
|
G | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2037G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088689 | ||||||
chr17:45088764
|
T | TAAA | 36 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(33): Show | 38 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.385+2112_385+2113i others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088764 | ||||||
chr17:45088765
|
T | A | 39 | a0001c0001t0004g0106a0001c0001t0005g0005a0001c0001t0005g0147others(36): Show | 41 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.385+2113T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088765 | ||||||
chr17:45088765
|
TA | T | 12 | a0001c0001t0028g0187a0001c0001t0028g0188a0001c0002t0001g0223others(9): Show | 12 | HG01109.hp2 HG01516.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.385+2128delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45088765 | |||||
chr17:45088766
|
A | T | 1 | a0001c0003t0020g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.385+2114A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088766 | ||||||
chr17:45088792
|
G | A | 10 | a0001c0004t0003g0133a0001c0004t0003g0135a0001c0004t0003g0136others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+2140G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088792 | ||||||
chr17:45088845
|
C | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2193C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088845 | ||||||
chr17:45089019
|
C | T | 4 | a0001c0003t0020g0097a0001c0003t0020g0098a0001c0003t0038g0096others(1): Show | 4 | HG01175.hp1 HG01261.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+2367C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089019 | ||||||
chr17:45089082
|
G | T | 242 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(239): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.385+2430G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089082 | ||||||
chr17:45089172
|
G | A | 1 | a0001c0004t0003g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.385+2520G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089172 | ||||||
chr17:45089342
|
G | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2690G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089342 | ||||||
chr17:45089454
|
G | A | 7 | a0001c0003t0002g0054a0001c0003t0011g0148a0001c0003t0011g0149others(4): Show | 7 | HG01891.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+2802G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089454 | ||||||
chr17:45089486
|
T | C | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2834T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089486 | ||||||
chr17:45089502
|
C | T | 1 | a0001c0004t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+2850C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089502 | ||||||
chr17:45089528
|
G | T | 2 | a0001c0003t0002g0044a0001c0003t0002g0045 | 2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.385+2876G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089528 | ||||||
chr17:45089789
|
C | T | 114 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.385+3137C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089789 | ||||||
chr17:45089918
|
G | T | 16 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0287others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.385+3266G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089918 | ||||||
chr17:45089925
|
A | G | 1 | a0001c0001t0007g0319 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.385+3273A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089925 | ||||||
chr17:45090106
|
G | C | 1 | a0001c0002t0001g0223 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.385+3454G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090106 | ||||||
chr17:45090112
|
G | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+3460G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090112 | ||||||
chr17:45090189
|
T | G | 1 | a0001c0003t0026g0056 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.386-3496T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090189 | ||||||
chr17:45090398
|
G | GTCGTTCT others(3): Show |
86 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(83): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.386-3285_386-3276d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45090398 | |||||
chr17:45090401
|
GTTC | G | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-3278_386-3276d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45090401 | |||||
chr17:45090495
|
G | C | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.386-3190G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090495 | ||||||
chr17:45090584
|
C | T | 49 | a0001c0003t0002g0002a0001c0003t0002g0022a0001c0003t0002g0023others(46): Show | 52 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.386-3101C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090584 | ||||||
chr17:45090906
|
A | G | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.386-2779A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090906 | ||||||
chr17:45091152
|
T | C | 1 | a0001c0004t0022g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.386-2533T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091152 | ||||||
chr17:45091157
|
G | A | 1 | a0001c0001t0050g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.386-2528G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091157 | ||||||
chr17:45091160
|
A | G | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2525A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091160 | ||||||
chr17:45091161
|
G | C | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2524G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091161 | ||||||
chr17:45091162
|
A | C | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2523A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091162 | ||||||
chr17:45091164
|
A | G | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2521A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091164 | ||||||
chr17:45091165
|
T | G | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2520T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091165 | ||||||
chr17:45091166
|
T | C | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2519T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091166 | ||||||
chr17:45091167
|
T | A | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2518T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091167 | ||||||
chr17:45091168
|
C | A | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2517C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091168 | ||||||
chr17:45091170
|
T | A | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2515T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091170 | ||||||
chr17:45091171
|
C | A | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2514C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091171 | ||||||
chr17:45091172
|
T | A | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2513T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091172 | ||||||
chr17:45091174
|
A | T | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2511A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091174 | ||||||
chr17:45091178
|
G | A | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2507G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091178 | ||||||
chr17:45091179
|
T | C | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2506T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091179 | ||||||
chr17:45091181
|
T | C | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2504T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091181 | ||||||
chr17:45091183
|
T | G | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2502T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091183 | ||||||
chr17:45091184
|
C | T | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2501C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091184 | ||||||
chr17:45091187
|
G | C | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2498G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091187 | ||||||
chr17:45091187
|
G | GAC | 22 | a0001c0001t0004g0110a0001c0001t0006g0329a0001c0001t0006g0330others(19): Show | 22 | HG00323.hp1 HG00609.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.386-2449_386-2448d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACAC | 29 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0013g0343others(26): Show | 30 | HG00544.hp1 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.386-2451_386-2448d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACAC | 11 | a0001c0001t0004g0118a0001c0001t0006g0345a0001c0001t0013g0318others(8): Show | 11 | HG01123.hp1 HG01516.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.386-2453_386-2448d others(8): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(1): Show |
15 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0004g0107others(12): Show | 15 | HG00408.hp1 HG00735.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-2455_386-2448d others(10): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(3): Show |
16 | a0001c0001t0002g0309a0001c0002t0001g0082a0001c0002t0001g0166others(13): Show | 16 | HG00140.hp2 HG01069.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.386-2457_386-2448d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(5): Show |
21 | a0001c0001t0002g0308a0001c0001t0006g0317a0001c0001t0049g0303others(18): Show | 22 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.386-2459_386-2448d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(7): Show |
12 | a0001c0002t0001g0167a0001c0002t0001g0169a0001c0002t0001g0172others(9): Show | 12 | HG00438.hp2 HG00609.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.386-2461_386-2448d others(16): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(9): Show |
12 | a0001c0001t0006g0340a0001c0002t0001g0079a0001c0002t0001g0092others(9): Show | 12 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-2463_386-2448d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(11): Show |
5 | a0001c0001t0002g0305a0001c0002t0001g0078a0001c0002t0001g0216others(2): Show | 5 | HG03098.hp1 NA18986.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-2465_386-2448d others(20): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(13): Show |
3 | a0001c0002t0001g0162a0001c0002t0001g0179a0001c0002t0024g0164 | 3 | HG01433.hp1 NA19054.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.386-2467_386-2448d others(22): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(15): Show |
1 | a0001c0002t0001g0170 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.386-2469_386-2448d others(24): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
G | GACACACA others(17): Show |
2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | NA18947.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.386-2471_386-2448d others(26): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GAC | G | 72 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0069others(69): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.386-2449_386-2448d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACAC | G | 29 | a0001c0001t0004g0071a0001c0001t0005g0259a0001c0001t0005g0266others(26): Show | 32 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.386-2451_386-2448d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACACAC | G | 6 | a0001c0001t0008g0291a0001c0001t0008g0297a0001c0001t0010g0018others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-2453_386-2448d others(8): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACACACA others(3): Show |
G | 3 | a0001c0001t0002g0020a0001c0001t0007g0322a0001c0003t0002g0052 | 3 | HG03516.hp1 NA18747.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.386-2457_386-2448d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACACACA others(5): Show |
G | 17 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(14): Show | 20 | HG00558.hp1 HG00673.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2459_386-2448d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACACACA others(7): Show |
G | 2 | a0001c0001t0004g0073a0001c0001t0004g0074 | 2 | NA18966.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.386-2461_386-2448d others(16): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACACACA others(9): Show |
G | 1 | a0001c0004t0053g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.386-2463_386-2448d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091187
|
GACACACA others(11): Show |
G | 2 | a0001c0004t0003g0013a0001c0004t0003g0214 | 3 | HG02257.hp2 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.386-2465_386-2448d others(20): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | |||||
chr17:45091188
|
A | T | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2497A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091188 | ||||||
chr17:45091190
|
A | T | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2495A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091190 | ||||||
chr17:45091192
|
A | T | 1 | a0001c0001t0005g0276 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2493A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091192 | ||||||
chr17:45091236
|
A | G | 30 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(27): Show | 32 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.386-2449A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091236 | ||||||
chr17:45091237
|
C | CGT | 7 | a0001c0001t0005g0260a0001c0001t0005g0273a0001c0001t0005g0274others(4): Show | 7 | HG00423.hp1 HG01361.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.386-2447_386-2446d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091237 | |||||
chr17:45091237
|
C | T | 30 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(27): Show | 32 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.386-2448C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091237 | ||||||
chr17:45091358
|
C | A | 1 | a0001c0004t0017g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.386-2327C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091358 | ||||||
chr17:45091388
|
T | G | 9 | a0001c0004t0003g0132a0001c0004t0003g0141a0001c0004t0003g0154others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-2297T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091388 | ||||||
chr17:45091597
|
G | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-2088G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091597 | ||||||
chr17:45091680
|
C | G | 1 | a0001c0004t0003g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.386-2005C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091680 | ||||||
chr17:45091694
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.386-1991T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091694 | ||||||
chr17:45091698
|
C | G | 1 | a0001c0003t0041g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.386-1987C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091698 | ||||||
chr17:45091741
|
T | A | 114 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(111): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.386-1944T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091741 | ||||||
chr17:45091913
|
C | G | 55 | a0001c0004t0003g0001a0001c0004t0003g0010a0001c0004t0003g0011others(52): Show | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.386-1772C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091913 | ||||||
chr17:45092024
|
A | G | 242 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(239): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.386-1661A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092024 | ||||||
chr17:45092186
|
A | G | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1499A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092186 | ||||||
chr17:45092219
|
AGGGACTT | A | 11 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(8): Show | 14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.386-1463_386-1457d others(9): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092219 | |||||
chr17:45092316
|
G | A | 1 | a0001c0003t0040g0353 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.386-1369G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092316 | ||||||
chr17:45092336
|
G | A | 1 | a0001c0003t0002g0038 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.386-1349G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092336 | ||||||
chr17:45092346
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.386-1339C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092346 | ||||||
chr17:45092347
|
G | A | 9 | a0001c0002t0001g0093a0001c0002t0001g0217a0001c0002t0001g0218others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-1338G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092347 | ||||||
chr17:45092397
|
AT | A | 100 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(97): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.386-1287delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092397 | ||||||
chr17:45092536
|
G | GA | 43 | a0001c0001t0004g0108a0001c0001t0005g0005a0001c0001t0005g0147others(40): Show | 45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.386-1137dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092536 | |||||
chr17:45092544
|
A | C | 2 | a0001c0002t0025g0081a0001c0002t0025g0180 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.386-1141A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092544 | ||||||
chr17:45092548
|
A | C | 1 | a0001c0001t0030g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.386-1137A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092548 | ||||||
chr17:45092571
|
G | A | 47 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(44): Show | 49 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.386-1114G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092571 | ||||||
chr17:45092602
|
C | A | 1 | a0001c0002t0004g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.386-1083C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092602 | ||||||
chr17:45092602
|
C | T | 6 | a0001c0003t0011g0148a0001c0003t0011g0149a0001c0003t0011g0150others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1083C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092602 | ||||||
chr17:45092707
|
CA | C | 217 | a0001c0001t0001g0111a0001c0001t0004g0003a0001c0001t0004g0004others(214): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.386-964delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092707 | |||||
chr17:45092716
|
AAAAAAG | A | 94 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(91): Show | 97 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.386-964_386-959del others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092716 | |||||
chr17:45093054
|
G | A | 86 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(83): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.386-631G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093054 | ||||||
chr17:45093099
|
A | G | 354 | a0001c0001t0001g0111a0001c0001t0002g0020a0001c0001t0002g0129others(351): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.386-586A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093099 | ||||||
chr17:45093301
|
G | A | 1 | a0001c0004t0053g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.386-384G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093301 | ||||||
chr17:45093539
|
C | T | 323 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(320): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.386-146C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093539 | ||||||
chr17:45093673
|
C | G | 1 | a0001c0004t0003g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.386-12C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093673 | ||||||
chr17:45093866
|
G | C | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+63G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45093866 | ||||||
chr17:45093881
|
C | T | 2 | a0001c0004t0003g0245a0001c0004t0003g0246 | 2 | NA18940.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.504+78C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45093881 | ||||||
chr17:45093936
|
G | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504+133G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45093936 | ||||||
chr17:45094153
|
C | G | 93 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(90): Show | 96 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.504+350C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094153 | ||||||
chr17:45094270
|
G | A | 1 | a0001c0004t0003g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.504+467G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094270 | ||||||
chr17:45094366
|
C | T | 93 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(90): Show | 96 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.504+563C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094366 | ||||||
chr17:45094466
|
C | G | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+663C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094466 | ||||||
chr17:45094494
|
C | CA | 6 | a0001c0001t0010g0315a0001c0001t0021g0299a0001c0001t0037g0313others(3): Show | 6 | HG00735.hp1 HG01099.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+705dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45094494 | |||||
chr17:45094518
|
A | AT | 9 | a0001c0001t0005g0276a0001c0001t0010g0018a0001c0001t0010g0315others(6): Show | 9 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+729dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45094518 | |||||
chr17:45094518
|
A | T | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+715A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094518 | ||||||
chr17:45094814
|
C | CT | 109 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(106): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.504+1027dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45094814 | |||||
chr17:45094839
|
G | A | 1 | a0001c0001t0006g0324 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.504+1036G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094839 | ||||||
chr17:45094999
|
G | T | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.505-1195G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094999 | ||||||
chr17:45095110
|
CT | C | 107 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(104): Show | 111 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.505-1070delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45095110 | |||||
chr17:45095110
|
CTT | C | 135 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(132): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.505-1071_505-1070d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45095110 | |||||
chr17:45095263
|
C | T | 1 | a0001c0001t0005g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-931C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095263 | ||||||
chr17:45095393
|
C | A | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-801C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095393 | ||||||
chr17:45095481
|
T | C | 150 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(147): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.505-713T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095481 | ||||||
chr17:45095512
|
A | G | 1 | a0001c0001t0004g0116 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.505-682A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095512 | ||||||
chr17:45095538
|
A | G | 49 | a0001c0003t0002g0002a0001c0003t0002g0022a0001c0003t0002g0023others(46): Show | 52 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.505-656A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095538 | ||||||
chr17:45095566
|
A | G | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-628A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095566 | ||||||
chr17:45095763
|
C | G | 149 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(146): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.505-431C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095763 | ||||||
chr17:45095849
|
C | T | 1 | a0001c0001t0021g0299 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.505-345C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095849 | ||||||
chr17:45095850
|
G | A | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-344G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095850 | ||||||
chr17:45095905
|
T | C | 124 | a0001c0001t0005g0005a0001c0001t0005g0185a0001c0001t0005g0234others(121): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.505-289T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095905 | ||||||
chr17:45096148
|
A | G | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-46A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45096148 | ||||||
chr17:45096154
|
T | C | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.505-40T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45096154 | ||||||
chr17:45096182
|
A | C | 1 | a0001c0002t0004g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.505-12A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45096182 | ||||||
chr17:45096459
|
C | T | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.596+174C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096459 | ||||||
chr17:45096534
|
TCTGGTGA | T | 5 | a0001c0001t0010g0018a0001c0001t0010g0315a0001c0001t0037g0313others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+252_596+258del others(7): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 45096534 | |||||
chr17:45096673
|
C | T | 1 | a0001c0003t0011g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.596+388C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096673 | ||||||
chr17:45096705
|
C | G | 1 | a0001c0002t0001g0077 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.596+420C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096705 | ||||||
chr17:45096739
|
G | A | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.597-389G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096739 | ||||||
chr17:45096848
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.597-280G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096848 | ||||||
chr17:45096853
|
A | C | 7 | a0001c0003t0010g0026a0001c0003t0010g0094a0001c0003t0010g0186others(4): Show | 7 | HG01109.hp2 HG02886.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.597-275A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096853 | ||||||
chr17:45097436
|
C | A | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.713+192C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097436 | ||||||
chr17:45097567
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.713+323G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097567 | ||||||
chr17:45097687
|
C | T | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.713+443C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097687 | ||||||
chr17:45097733
|
C | G | 1 | a0001c0002t0001g0174 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.713+489C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097733 | ||||||
chr17:45097794
|
G | A | 86 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(83): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.713+550G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097794 | ||||||
chr17:45097796
|
C | T | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.713+552C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097796 | ||||||
chr17:45098301
|
G | A | 1 | a0001c0003t0019g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714-81G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45098301 | ||||||
chr17:45098954
|
T | C | 2 | a0001c0001t0016g0258a0001c0001t0016g0292 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.884+402T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45098954 | ||||||
chr17:45098955
|
C | G | 3 | a0001c0001t0008g0287a0001c0001t0029g0255a0001c0001t0029g0256 | 3 | HG03209.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.884+403C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45098955 | ||||||
chr17:45099040
|
G | A | 1 | a0001c0003t0002g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.885-365G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099040 | ||||||
chr17:45099160
|
C | T | 5 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(2): Show | 5 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.885-245C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099160 | ||||||
chr17:45099241
|
C | T | 1 | a0001c0003t0002g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.885-164C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099241 | ||||||
chr17:45099254
|
G | A | 52 | a0001c0004t0003g0001a0001c0004t0003g0010a0001c0004t0003g0011others(49): Show | 64 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.885-151G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099254 | ||||||
chr17:45099264
|
A | C | 89 | a0001c0001t0006g0193a0001c0001t0006g0317a0001c0001t0006g0324others(86): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.885-141A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099264 | ||||||
chr17:45099288
|
C | T | 1 | a0001c0001t0008g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.885-117C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099288 | ||||||
chr17:45099385
|
G | A | 1 | a0001c0002t0001g0226 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.885-20G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099385 | ||||||
chr17:45099894
|
C | T | 2 | a0001c0002t0001g0202a0001c0002t0018g0212 | 2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.993+381C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45099894 | ||||||
chr17:45099945
|
C | T | 1 | a0001c0001t0006g0336 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.993+432C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45099945 | ||||||
chr17:45100110
|
A | G | 1 | a0001c0004t0003g0248 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.993+597A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100110 | ||||||
chr17:45100352
|
A | G | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.993+839A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100352 | ||||||
chr17:45100527
|
C | T | 1 | a0001c0004t0003g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.993+1014C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100527 | ||||||
chr17:45100583
|
T | C | 241 | a0001c0001t0002g0020a0001c0001t0002g0129a0001c0001t0002g0227others(238): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.993+1070T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100583 | ||||||
chr17:45100626
|
C | T | 51 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(48): Show | 54 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.993+1113C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100626 | ||||||
chr17:45100659
|
A | C | 1 | a0001c0002t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.993+1146A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100659 | ||||||
chr17:45100678
|
G | A | 2 | a0001c0003t0002g0225a0001c0003t0002g0352 | 2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.993+1165G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100678 | ||||||
chr17:45100721
|
C | T | 1 | a0001c0004t0032g0014 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.993+1208C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100721 | ||||||
chr17:45100862
|
C | CA | 36 | a0001c0001t0004g0003a0001c0001t0004g0072a0001c0001t0004g0074others(33): Show | 38 | HG00544.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.993+1383dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
C | CAA | 30 | a0001c0001t0004g0065a0001c0001t0004g0073a0001c0001t0004g0107others(27): Show | 33 | HG00408.hp1 HG01070.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.993+1382_993+1383d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
C | CAAA | 16 | a0001c0001t0004g0071a0001c0003t0002g0022a0001c0003t0002g0023others(13): Show | 16 | HG00438.hp2 HG00597.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.993+1381_993+1383d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
C | CAAAA | 10 | a0001c0003t0002g0030a0001c0003t0002g0031a0001c0003t0002g0036others(7): Show | 10 | HG00423.hp2 HG00609.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.993+1380_993+1383d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CA | C | 39 | a0001c0001t0001g0111a0001c0001t0004g0119a0001c0001t0009g0131others(36): Show | 40 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.993+1383delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAA | C | 10 | a0001c0002t0001g0085a0001c0002t0001g0091a0001c0002t0001g0215others(7): Show | 10 | HG01243.hp2 HG01943.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.993+1382_993+1383d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAA | C | 15 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(12): Show | 15 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.993+1380_993+1383d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAA | C | 15 | a0001c0001t0005g0236a0001c0001t0005g0266a0001c0001t0005g0275others(12): Show | 16 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.993+1379_993+1383d others(7): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAA | C | 31 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(28): Show | 33 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.993+1378_993+1383d others(8): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA | C | 9 | a0001c0001t0005g0263a0001c0001t0007g0006a0001c0001t0007g0007others(6): Show | 12 | HG00558.hp1 HG01255.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.993+1377_993+1383d others(9): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0006g0333a0001c0001t0006g0340a0001c0001t0007g0316others(6): Show | 9 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.993+1376_993+1383d others(10): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(2): Show |
C | 72 | a0001c0001t0006g0317a0001c0001t0006g0324a0001c0001t0006g0325others(69): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.993+1375_993+1383d others(11): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0006g0193a0001c0001t0051g0328a0001c0004t0003g0011others(4): Show | 9 | HG00280.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.993+1374_993+1383d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0019g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.993+1373_993+1383d others(13): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0028g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.993+1372_993+1383d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0028g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.993+1371_993+1383d others(15): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(7): Show |
C | 6 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(3): Show | 6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+1370_993+1383d others(16): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(8): Show |
C | 8 | a0001c0001t0004g0004a0001c0001t0004g0069a0001c0001t0004g0106others(5): Show | 10 | HG01109.hp1 HG01928.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.993+1369_993+1383d others(17): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0009g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.993+1368_993+1383d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100862
|
CAAAAAAA others(15): Show |
C | 4 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(1): Show | 4 | HG01074.hp1 HG01106.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+1362_993+1383d others(24): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | |||||
chr17:45100896
|
A | G | 1 | a0001c0001t0004g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993+1383A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100896 | ||||||
chr17:45100897
|
G | A | 1 | a0001c0001t0004g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993+1384G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100897 | ||||||
chr17:45100899
|
A | G | 1 | a0001c0001t0004g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993+1386A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100899 | ||||||
chr17:45101041
|
G | A | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.993+1528G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101041 | ||||||
chr17:45101076
|
C | T | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.993+1563C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101076 | ||||||
chr17:45101109
|
G | A | 2 | a0001c0001t0028g0187a0001c0001t0028g0188 | 2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.993+1596G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101109 | ||||||
chr17:45101140
|
C | A | 1 | a0001c0003t0010g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.993+1627C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101140 | ||||||
chr17:45101216
|
G | A | 1 | a0001c0001t0050g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.993+1703G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101216 | ||||||
chr17:45101226
|
C | T | 1 | a0001c0004t0014g0250 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.993+1713C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101226 | ||||||
chr17:45101298
|
A | G | 16 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(13): Show | 19 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.994-1653A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101298 | ||||||
chr17:45101341
|
T | C | 2 | a0001c0001t0008g0291a0001c0001t0008g0297 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.994-1610T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101341 | ||||||
chr17:45101362
|
C | T | 1 | a0001c0003t0002g0024 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.994-1589C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101362 | ||||||
chr17:45101363
|
G | T | 1 | a0001c0003t0002g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.994-1588G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101363 | ||||||
chr17:45101461
|
A | G | 6 | a0001c0002t0001g0079a0001c0002t0001g0162a0001c0002t0001g0169others(3): Show | 6 | HG02083.hp1 HG02155.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-1490A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101461 | ||||||
chr17:45101496
|
G | A | 7 | a0001c0003t0010g0026a0001c0003t0010g0094a0001c0003t0010g0186others(4): Show | 7 | HG01109.hp2 HG02886.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-1455G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101496 | ||||||
chr17:45101547
|
A | AG | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.994-1402dupG | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101547 | |||||
chr17:45101563
|
G | A | 1 | a0001c0003t0002g0024 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.994-1388G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101563 | ||||||
chr17:45101574
|
G | A | 1 | a0001c0003t0002g0352 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-1377G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101574 | ||||||
chr17:45101617
|
C | CA | 85 | a0001c0001t0002g0304a0001c0001t0002g0306a0001c0001t0002g0307others(82): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.994-1312dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101617 | |||||
chr17:45101617
|
C | CAA | 12 | a0001c0001t0002g0020a0001c0001t0002g0305a0001c0001t0002g0309others(9): Show | 12 | HG00423.hp1 HG01361.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.994-1313_994-1312d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101617 | |||||
chr17:45101617
|
CA | C | 72 | a0001c0002t0001g0008a0001c0002t0001g0049a0001c0002t0001g0067others(69): Show | 73 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.994-1312delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101617 | |||||
chr17:45101678
|
C | A | 1 | a0001c0003t0041g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.994-1273C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101678 | ||||||
chr17:45101687
|
A | G | 2 | a0001c0001t0010g0315a0001c0001t0037g0313 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.994-1264A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101687 | ||||||
chr17:45101700
|
G | A | 1 | a0001c0001t0005g0263 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.994-1251G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101700 | ||||||
chr17:45101938
|
G | T | 10 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0316others(7): Show | 13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.994-1013G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101938 | ||||||
chr17:45102149
|
C | T | 1 | a0001c0003t0002g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.994-802C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102149 | ||||||
chr17:45102166
|
A | G | 1 | a0001c0001t0005g0234 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.994-785A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102166 | ||||||
chr17:45102294
|
G | A | 10 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.994-657G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102294 | ||||||
chr17:45102306
|
A | G | 75 | a0001c0001t0002g0020a0001c0001t0008g0017a0001c0001t0008g0257others(72): Show | 79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.994-645A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102306 | ||||||
chr17:45102816
|
G | C | 1 | a0001c0001t0005g0273 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.994-135G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102816 | ||||||
chr17:45102834
|
G | A | 1 | a0001c0001t0030g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.994-117G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102834 | ||||||
chr17:45103203
|
A | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+82A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103203 | ||||||
chr17:45103249
|
C | T | 55 | a0001c0004t0003g0001a0001c0004t0003g0010a0001c0004t0003g0011others(52): Show | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1164+128C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103249 | ||||||
chr17:45103479
|
G | A | 4 | a0001c0001t0002g0310a0001c0005t0002g0021a0001c0005t0002g0282others(1): Show | 4 | HG02145.hp1 NA18941.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-230G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103479 | ||||||
chr17:45103610
|
G | T | 3 | a0001c0002t0004g0231a0001c0002t0004g0232a0001c0002t0004g0233 | 3 | HG00140.hp2 HG01361.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1165-99G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103610 | ||||||
chr17:45103890
|
G | A | 1 | a0001c0001t0016g0295 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1332+14G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103890 | ||||||
chr17:45103895
|
G | T | 16 | a0001c0001t0002g0129a0001c0001t0002g0227a0001c0001t0002g0228others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332+19G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103895 | ||||||
chr17:45103919
|
A | G | 355 | a0001c0001t0001g0111a0001c0001t0002g0020a0001c0001t0002g0129others(352): Show | 382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.1332+43A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103919 | ||||||
chr17:45103957
|
A | G | 38 | a0001c0001t0005g0005a0001c0001t0005g0147a0001c0001t0005g0185others(35): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1332+81A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103957 | ||||||
chr17:45104256
|
C | T | 2 | a0001c0003t0002g0033a0001c0003t0002g0064 | 2 | NA18960.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1332+380C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104256 | ||||||
chr17:45104264
|
G | A | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1332+388G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104264 | ||||||
chr17:45104569
|
TAG | T | 34 | a0001c0001t0001g0111a0001c0001t0004g0003a0001c0001t0004g0004others(31): Show | 38 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1333-287_1333-286d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 45104569 | |||||
chr17:45104634
|
G | A | 1 | a0001c0001t0009g0131 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1333-225G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104634 | ||||||
chr17:45104650
|
A | C | 1 | a0001c0004t0003g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1333-209A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104650 | ||||||
chr17:45104697
|
C | A | 1 | a0001c0001t0002g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1333-162C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104697 | ||||||
chr17:45104747
|
C | A | 5 | a0001c0001t0010g0018a0001c0001t0010g0315a0001c0001t0037g0313others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-112C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104747 | ||||||
chr17:45105112
|
T | C | 1 | a0001c0001t0037g0313 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1470+116T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105112 | ||||||
chr17:45105238
|
A | C | 1 | a0001c0004t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1470+242A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105238 | ||||||
chr17:45105261
|
G | A | 1 | a0001c0001t0004g0114 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1470+265G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105261 | ||||||
chr17:45105442
|
T | G | 75 | a0001c0001t0002g0020a0001c0001t0008g0287a0001c0001t0029g0255others(72): Show | 78 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1471-177T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105442 | ||||||
chr17:45105524
|
G | A | 13 | a0001c0001t0008g0017a0001c0001t0008g0257a0001c0001t0008g0288others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1471-95G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105524 |