geneid | 9397 |
---|---|
ensemblid | ENSG00000152465.18 |
hgncid | 7858 |
symbol | NMT2 |
name | N-myristoyltransferase 2 |
refseq_nuc | NM_004808.3 |
refseq_prot | NP_004799.1 |
ensembl_nuc | ENST00000378165.9 |
ensembl_prot | ENSP00000367407.3 |
mane_status | MANE Select |
chr | chr10 |
start | 15105770 |
end | 15168693 |
strand | - |
ver | v1.2 |
region | chr10:15105770-15168693 |
region5000 | chr10:15100770-15173693 |
regionname0 | NMT2_chr10_15105770_15168693 |
regionname5000 | NMT2_chr10_15100770_15173693 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1497 | 233 | 60 | 48 | 89 | 12 | 22 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0002 | 0/0 | 1497 | 24 | 23 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0003 | 0/0 | 1497 | 5 | 0 | 0 | 5 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0004 | 0/0 | 1497 | 4 | 3 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0005 | 0/0 | 1497 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0006 | 0/0 | 1497 | 3 | 3 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0007 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0008 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
c0009 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3506 | 120 | 11 | 28 | 62 | 6 | 13 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0002 | 0/0 | 3505 | 17 | 4 | 2 | 10 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0003 | 0/0 | 3506 | 12 | 2 | 4 | 3 | 2 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0004 | 0/0 | 3506 | 11 | 5 | 1 | 3 | 0 | 2 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0005 | 0/0 | 3507 | 10 | 10 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0006 | 0/0 | 3509 | 9 | 8 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0007 | 1/1 | 3507 | 8 | 0 | 3 | 1 | 1 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0008 | 0/0 | 3507 | 7 | 0 | 0 | 7 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0009 | 0/0 | 3505 | 7 | 5 | 2 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0010 | 0/0 | 3503 | 6 | 6 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0011 | 0/0 | 3507 | 6 | 6 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0012 | 0/0 | 3508 | 5 | 2 | 1 | 0 | 2 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0013 | 0/0 | 3508 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0014 | 0/0 | 3508 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0015 | 0/0 | 3507 | 3 | 2 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0016 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0017 | 0/0 | 3508 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0018 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0019 | 0/0 | 3509 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0020 | 0/0 | 3506 | 2 | 0 | 2 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0021 | 0/0 | 3506 | 2 | 0 | 0 | 2 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0022 | 0/0 | 3506 | 2 | 1 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0023 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0024 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0025 | 0/0 | 3506 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0026 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0027 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0028 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0029 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0030 | 0/0 | 3508 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0031 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0032 | 0/0 | 3508 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0033 | 0/0 | 3508 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0034 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0035 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0036 | 0/0 | 3506 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0037 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0038 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0039 | 0/0 | 3506 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0040 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0041 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0042 | 0/0 | 3506 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0043 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0044 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0045 | 0/0 | 3506 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0046 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0047 | 0/0 | 3506 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0048 | 0/0 | 3505 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0049 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0050 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0051 | 0/0 | 3505 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0052 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0053 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0054 | 0/0 | 3493 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
t0055 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1497 | 233 | 60 | 48 | 89 | 12 | 22 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002 | 0/0 | 1497 | 24 | 23 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0003 | 0/0 | 1497 | 5 | 0 | 0 | 5 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0004 | 0/0 | 1497 | 4 | 3 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0005 | 0/0 | 1497 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0006 | 0/0 | 1497 | 3 | 3 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0007 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0009 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0002c0008 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5002 | 118 | 11 | 28 | 60 | 6 | 13 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0002 | 0/0 | 5001 | 14 | 1 | 2 | 10 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0003 | 0/0 | 5002 | 10 | 0 | 4 | 3 | 2 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0004 | 0/0 | 5002 | 11 | 5 | 1 | 3 | 0 | 2 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0005 | 0/0 | 5003 | 8 | 8 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0006 | 0/0 | 5005 | 9 | 8 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0007 | 1/1 | 5003 | 8 | 0 | 3 | 1 | 1 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0008 | 0/0 | 5003 | 4 | 0 | 0 | 4 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0009 | 0/0 | 5001 | 6 | 4 | 2 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0011 | 0/0 | 5003 | 5 | 5 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0012 | 0/0 | 5004 | 4 | 1 | 1 | 0 | 2 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0013 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0017 | 0/0 | 5004 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0020 | 0/0 | 5002 | 2 | 0 | 2 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0021 | 0/0 | 5002 | 2 | 0 | 0 | 2 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0022 | 0/0 | 5002 | 2 | 1 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0023 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0024 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0026 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0028 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0029 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0030 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0033 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0034 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0035 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0036 | 0/0 | 5002 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0037 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0038 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0039 | 0/0 | 5002 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0040 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0041 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0042 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0043 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0044 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0045 | 0/0 | 5002 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0046 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0047 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0049 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0050 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0051 | 0/0 | 5001 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0052 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0053 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0001t0054 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0002 | 0/0 | 5001 | 3 | 3 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0005 | 0/0 | 5003 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0010 | 0/0 | 4999 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0012 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0013 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0014 | 0/0 | 5004 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0015 | 0/0 | 5003 | 3 | 2 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0018 | 0/0 | 5003 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0019 | 0/0 | 5005 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0031 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0002t0032 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0003t0001 | 0/0 | 5002 | 2 | 0 | 0 | 2 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0003t0008 | 0/0 | 5003 | 3 | 0 | 0 | 3 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0004t0013 | 0/0 | 5004 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0004t0025 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0004t0048 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0005t0003 | 0/0 | 5002 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0005t0009 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0005t0010 | 0/0 | 4999 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0006t0016 | 0/0 | 5003 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0006t0027 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0007t0011 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0001c0009t0055 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
a0002c0008t0010 | 0/0 | 4999 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | copy fasta | chr10 | 15100770 | 15173693 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0012g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0017g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0017g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0020g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0020g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0021g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0022g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0022g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0023g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0024g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0028g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0029g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0033g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0034g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0035g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0036g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0037g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0038g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0039g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0040g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0041g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0042g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0043g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0044g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0045g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0046g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0047g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0049g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0050g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0051g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0052g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0053g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0001t0054g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0014g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0015g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0031g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0002t0032g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0003t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0003t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0003t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0004t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0004t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0004t0025g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0004t0048g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0005t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0005t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0005t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0005t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0006t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0006t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0006t0027g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0007t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0001c0009t0055g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
a0002c0008t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00099 | hp2 | a0001 | c0001 | t0007 | g0223 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0077 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00423 | hp2 | a0001 | c0003 | t0008 | g0146 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0092 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00558 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00639 | hp1 | a0001 | c0001 | t0009 | g0168 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0120 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00673 | hp1 | a0001 | c0003 | t0008 | g0248 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00738 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG00741 | hp2 | a0001 | c0001 | t0020 | g0065 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01109 | hp1 | a0001 | c0002 | t0015 | g0123 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01167 | hp2 | a0001 | c0001 | t0020 | g0068 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01175 | hp2 | a0001 | c0001 | t0051 | g0232 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01192 | hp2 | a0001 | c0001 | t0022 | g0080 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0260 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0262 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01261 | hp2 | a0001 | c0001 | t0012 | g0078 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01934 | hp2 | a0001 | c0001 | t0047 | g0197 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01975 | hp2 | a0001 | c0004 | t0025 | g0096 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02027 | hp2 | a0001 | c0001 | t0036 | g0243 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02055 | hp1 | a0001 | c0001 | t0026 | g0100 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02145 | hp1 | a0001 | c0001 | t0028 | g0118 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02145 | hp2 | a0001 | c0002 | t0018 | g0271 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02148 | hp1 | a0001 | c0001 | t0042 | g0225 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02257 | hp2 | a0001 | c0001 | t0009 | g0202 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02258 | hp2 | a0001 | c0002 | t0010 | g0090 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02280 | hp1 | a0001 | c0002 | t0014 | g0089 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0115 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02451 | hp1 | a0001 | c0001 | t0052 | g0067 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02523 | hp1 | a0001 | c0003 | t0008 | g0150 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02523 | hp2 | a0001 | c0001 | t0008 | g0246 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0258 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02572 | hp2 | a0001 | c0004 | t0013 | g0113 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02615 | hp1 | a0001 | c0002 | t0031 | g0270 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02622 | hp1 | a0001 | c0007 | t0011 | g0121 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0143 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02630 | hp2 | a0001 | c0001 | t0035 | g0114 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02647 | hp1 | a0001 | c0002 | t0010 | g0012 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02698 | hp2 | a0001 | c0001 | t0046 | g0154 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0275 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02723 | hp2 | a0001 | c0001 | t0023 | g0001 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02735 | hp2 | a0001 | c0001 | t0038 | g0183 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0255 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02818 | hp2 | a0001 | c0001 | t0017 | g0228 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02886 | hp1 | a0001 | c0002 | t0013 | g0099 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02896 | hp2 | a0001 | c0004 | t0013 | g0112 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02965 | hp1 | a0001 | c0004 | t0048 | g0016 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02970 | hp1 | a0001 | c0006 | t0016 | g0014 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02976 | hp1 | a0001 | c0002 | t0019 | g0131 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0142 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03098 | hp1 | a0001 | c0005 | t0003 | g0129 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03098 | hp2 | a0001 | c0005 | t0009 | g0128 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03130 | hp1 | a0001 | c0002 | t0010 | g0126 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03130 | hp2 | a0001 | c0002 | t0014 | g0073 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03139 | hp1 | a0001 | c0002 | t0014 | g0087 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03139 | hp2 | a0001 | c0001 | t0049 | g0206 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03195 | hp2 | a0001 | c0002 | t0032 | g0101 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0111 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03225 | hp1 | a0001 | c0002 | t0019 | g0130 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03225 | hp2 | a0001 | c0002 | t0010 | g0011 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03453 | hp1 | a0001 | c0005 | t0003 | g0125 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03453 | hp2 | a0001 | c0001 | t0024 | g0074 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03486 | hp1 | a0001 | c0002 | t0012 | g0018 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0257 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03516 | hp2 | a0001 | c0002 | t0018 | g0268 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0122 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03540 | hp2 | a0001 | c0001 | t0050 | g0239 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0249 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03688 | hp1 | a0001 | c0001 | t0053 | g0006 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03927 | hp1 | a0001 | c0001 | t0029 | g0224 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18522 | hp1 | a0001 | c0001 | t0034 | g0098 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18522 | hp2 | a0001 | c0001 | t0043 | g0160 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0097 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18962 | hp2 | a0001 | c0001 | t0045 | g0050 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18972 | hp1 | a0001 | c0001 | t0054 | g0235 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18972 | hp2 | a0001 | c0001 | t0030 | g0082 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0264 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18977 | hp2 | a0001 | c0001 | t0021 | g0263 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18980 | hp2 | a0001 | c0001 | t0037 | g0179 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18982 | hp2 | a0001 | c0001 | t0039 | g0021 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19030 | hp2 | a0001 | c0006 | t0016 | g0010 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19043 | hp1 | a0001 | c0002 | t0014 | g0088 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19043 | hp2 | a0001 | c0006 | t0027 | g0015 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA19240 | hp2 | a0001 | c0002 | t0015 | g0102 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | ASW | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ASW | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20752 | hp1 | a0001 | c0001 | t0012 | g0079 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20752 | hp2 | a0001 | c0001 | t0041 | g0044 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0152 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02109 | hp1 | a0001 | c0001 | t0033 | g0107 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02486 | hp1 | a0001 | c0001 | t0044 | g0116 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02486 | hp2 | a0001 | c0001 | t0022 | g0086 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02559 | hp1 | a0001 | c0002 | t0015 | g0124 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03471 | hp1 | a0001 | c0005 | t0010 | g0045 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
HG06807 | hp2 | a0001 | c0002 | t0005 | g0276 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18955 | hp1 | a0001 | c0001 | t0021 | g0051 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA20300 | hp2 | a0002 | c0008 | t0010 | g0013 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA21309 | hp1 | a0001 | c0009 | t0055 | g0022 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
NA21309 | hp2 | a0001 | c0001 | t0040 | g0062 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0198 | REF | REF | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0178 | REF | REF | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:15119491
|
C | G | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1022G>C | p.Arg341Thr | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/12 | 1103/5003 | 1022/1497 | 341/498 | chr10 | 15119491 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:15112871
|
G | C | 1 | a0001c0007 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1263C>G | p.Ala421Ala | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/12 | 1344/5003 | 1263/1497 | 421/498 | chr10 | 15112871 | ||
chr10:15128427
|
A | G | 1 | a0001c0006 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.922T>C | p.Leu308Leu | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/12 | 1003/5003 | 922/1497 | 308/498 | chr10 | 15128427 | ||
chr10:15130273
|
A | G | 1 | a0001c0003 | 5 | HG00423.hp2 HG00673.hp1 HG02083.hp1 others(2): Show |
synonymous_variant | LOW | c.759T>C | p.His253His | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/12 | 840/5003 | 759/1497 | 253/498 | chr10 | 15130273 | ||
chr10:15133067
|
G | A | 1 | a0001c0004 | 4 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.588C>T | p.Pro196Pro | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 5/12 | 669/5003 | 588/1497 | 196/498 | chr10 | 15133067 | ||
chr10:15135281
|
T | C | 4 | a0001c0002a0001c0005a0001c0009others(1): Show | 30 | HG01109.hp1 HG01891.hp1 HG02145.hp2 others(27): Show |
synonymous_variant | LOW | c.384A>G | p.Pro128Pro | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/12 | 465/5003 | 384/1497 | 128/498 | chr10 | 15135281 | ||
chr10:15135340
|
T | G | 1 | a0001c0009 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.325A>C | p.Arg109Arg | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/12 | 406/5003 | 325/1497 | 109/498 | chr10 | 15135340 | ||
chr10:15141464
|
C | T | 2 | a0001c0004a0001c0005 | 8 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
synonymous_variant | LOW | c.204G>A | p.Ser68Ser | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/12 | 285/5003 | 204/1497 | 68/498 | chr10 | 15141464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:15105818
|
A | G | 2 | a0001c0002t0014a0001c0002t0019 | 6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3377T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3377 | chr10 | 15105818 | |||||
chr10:15105869
|
GTTA | G | 3 | a0001c0002t0010a0001c0005t0010a0002c0008t0010 | 6 | HG02258.hp2 HG02647.hp1 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3323_*3325delTAA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3323 | chr10 | 15105869 | |||||
chr10:15105914
|
T | C | 3 | a0001c0001t0049a0001c0002t0015a0001c0002t0032 | 5 | HG01109.hp1 HG02559.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3281A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3281 | chr10 | 15105914 | |||||
chr10:15105966
|
T | A | 4 | a0001c0001t0006a0001c0001t0028a0001c0001t0033others(1): Show | 12 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3229A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3229 | chr10 | 15105966 | |||||
chr10:15106064
|
G | C | 9 | a0001c0001t0005a0001c0001t0011a0001c0001t0023others(6): Show | 21 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3131C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3131 | chr10 | 15106064 | |||||
chr10:15106080
|
G | A | 2 | a0001c0002t0014a0001c0002t0019 | 6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3115C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3115 | chr10 | 15106080 | |||||
chr10:15106097
|
G | A | 1 | a0001c0001t0026 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3098C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3098 | chr10 | 15106097 | |||||
chr10:15106116
|
C | T | 3 | a0001c0001t0002a0001c0001t0037a0001c0002t0002 | 18 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3079G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3079 | chr10 | 15106116 | |||||
chr10:15106144
|
C | G | 4 | a0001c0001t0006a0001c0001t0028a0001c0001t0033others(1): Show | 12 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3051 | chr10 | 15106144 | |||||
chr10:15106149
|
A | G | 49 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(46): Show | 126 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*3046T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3046 | chr10 | 15106149 | |||||
chr10:15106166
|
G | A | 1 | a0001c0001t0041 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3029C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3029 | chr10 | 15106166 | |||||
chr10:15106224
|
ACCTCAAG others(6): Show |
A | 1 | a0001c0001t0054 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2958_*2970delAGAT others(9): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2958 | chr10 | 15106224 | |||||
chr10:15106239
|
C | T | 2 | a0001c0001t0004a0001c0001t0034 | 12 | HG01243.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2956G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2956 | chr10 | 15106239 | |||||
chr10:15106284
|
C | T | 4 | a0001c0001t0009a0001c0001t0051a0001c0001t0052others(1): Show | 9 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2911G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2911 | chr10 | 15106284 | |||||
chr10:15106327
|
T | C | 1 | a0001c0001t0042 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2868A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2868 | chr10 | 15106327 | |||||
chr10:15106354
|
GA | G | 1 | a0001c0002t0015 | 3 | HG01109.hp1 HG02559.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2840delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2840 | chr10 | 15106354 | |||||
chr10:15106509
|
G | A | 1 | a0001c0004t0048 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2686C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2686 | chr10 | 15106509 | |||||
chr10:15106548
|
G | A | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | 125 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2647C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2647 | chr10 | 15106548 | |||||
chr10:15106580
|
A | T | 15 | a0001c0001t0006a0001c0001t0012a0001c0001t0013others(12): Show | 33 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2615T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2615 | chr10 | 15106580 | |||||
chr10:15106639
|
C | T | 1 | a0001c0001t0039 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2556G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2556 | chr10 | 15106639 | |||||
chr10:15106671
|
T | A | 1 | a0001c0002t0032 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2524A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2524 | chr10 | 15106671 | |||||
chr10:15106673
|
C | T | 1 | a0001c0001t0038 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2522 | chr10 | 15106673 | |||||
chr10:15106903
|
C | A | 9 | a0001c0001t0005a0001c0001t0011a0001c0001t0023others(6): Show | 21 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2292G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2292 | chr10 | 15106903 | |||||
chr10:15106908
|
A | C | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(16): Show | 52 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2287T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2287 | chr10 | 15106908 | |||||
chr10:15106961
|
C | T | 2 | a0001c0002t0018a0001c0004t0048 | 3 | HG02145.hp2 HG02965.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2234G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2234 | chr10 | 15106961 | |||||
chr10:15107009
|
G | A | 1 | a0001c0001t0020 | 2 | HG00741.hp2 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2186C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2186 | chr10 | 15107009 | |||||
chr10:15107081
|
C | T | 1 | a0001c0001t0051 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2114G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2114 | chr10 | 15107081 | |||||
chr10:15107089
|
A | G | 1 | a0001c0001t0045 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2106T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2106 | chr10 | 15107089 | |||||
chr10:15107101
|
C | G | 3 | a0001c0001t0002a0001c0001t0037a0001c0002t0002 | 18 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2094G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2094 | chr10 | 15107101 | |||||
chr10:15107108
|
TA | T | 44 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(41): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2086delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2086 | chr10 | 15107108 | |||||
chr10:15107108
|
TAA | T | 6 | a0001c0001t0002a0001c0001t0009a0001c0001t0051others(3): Show | 26 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2086delTT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2085 | chr10 | 15107108 | |||||
chr10:15107166
|
C | T | 24 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(21): Show | 63 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2029G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2029 | chr10 | 15107166 | |||||
chr10:15107366
|
T | C | 1 | a0001c0001t0044 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1829A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1829 | chr10 | 15107366 | |||||
chr10:15107541
|
C | T | 1 | a0001c0001t0036 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1654G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1654 | chr10 | 15107541 | |||||
chr10:15107607
|
A | G | 4 | a0001c0001t0013a0001c0001t0035a0001c0002t0013others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1588T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1588 | chr10 | 15107607 | |||||
chr10:15107657
|
G | A | 7 | a0001c0001t0005a0001c0001t0011a0001c0001t0023others(4): Show | 19 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1538C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1538 | chr10 | 15107657 | |||||
chr10:15107710
|
C | T | 1 | a0001c0002t0019 | 2 | HG02976.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1485G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1485 | chr10 | 15107710 | |||||
chr10:15107714
|
C | G | 1 | a0001c0001t0034 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1481 | chr10 | 15107714 | |||||
chr10:15107776
|
C | CT | 17 | a0001c0001t0006a0001c0001t0012a0001c0001t0013others(14): Show | 37 | HG00140.hp2 HG00642.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1418dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1418 | chr10 | 15107776 | |||||
chr10:15107978
|
C | A | 3 | a0001c0001t0021a0001c0001t0045a0001c0001t0047 | 4 | HG01934.hp2 NA18955.hp1 NA18962.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1217G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1217 | chr10 | 15107978 | |||||
chr10:15107981
|
C | T | 5 | a0001c0001t0006a0001c0001t0012a0001c0001t0030others(2): Show | 16 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1214G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1214 | chr10 | 15107981 | |||||
chr10:15108185
|
T | G | 2 | a0001c0006t0016a0001c0006t0027 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1010A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1010 | chr10 | 15108185 | |||||
chr10:15108186
|
T | C | 2 | a0001c0006t0016a0001c0006t0027 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1009A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1009 | chr10 | 15108186 | |||||
chr10:15108188
|
C | CT | 16 | a0001c0001t0006a0001c0001t0008a0001c0001t0012others(13): Show | 40 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1006dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1006 | chr10 | 15108188 | |||||
chr10:15108269
|
C | T | 1 | a0001c0001t0029 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*926G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 926 | chr10 | 15108269 | |||||
chr10:15108392
|
G | A | 3 | a0001c0001t0017a0001c0001t0046a0001c0001t0047 | 4 | HG01934.hp2 HG02572.hp1 HG02698.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*803C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 803 | chr10 | 15108392 | |||||
chr10:15108440
|
C | A | 1 | a0001c0004t0048 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 755 | chr10 | 15108440 | |||||
chr10:15108463
|
G | A | 1 | a0001c0001t0049 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 732 | chr10 | 15108463 | |||||
chr10:15108465
|
G | A | 1 | a0001c0001t0050 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 730 | chr10 | 15108465 | |||||
chr10:15108495
|
T | A | 6 | a0001c0001t0009a0001c0001t0022a0001c0001t0028others(3): Show | 12 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*700A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 700 | chr10 | 15108495 | |||||
chr10:15108692
|
G | A | 1 | a0001c0002t0018 | 2 | HG02145.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*503C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 503 | chr10 | 15108692 | |||||
chr10:15108734
|
A | G | 13 | a0001c0001t0005a0001c0001t0013a0001c0001t0017others(10): Show | 25 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*461T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 461 | chr10 | 15108734 | |||||
chr10:15108859
|
G | C | 1 | a0001c0001t0053 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*336C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 336 | chr10 | 15108859 | |||||
chr10:15108940
|
G | A | 1 | a0001c0001t0054 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 255 | chr10 | 15108940 | |||||
chr10:15109036
|
G | A | 1 | a0001c0009t0055 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 159 | chr10 | 15109036 | |||||
chr10:15168666
|
A | T | 1 | a0001c0001t0023 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/12 | 54 | chr10 | 15168666 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:15109227
|
G | A | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1477-12C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109227 | ||||||
chr10:15109229
|
A | G | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1477-14T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109229 | ||||||
chr10:15109230
|
G | A | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1477-15C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109230 | ||||||
chr10:15109349
|
C | A | 9 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(6): Show | 9 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1477-134G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109349 | ||||||
chr10:15109349
|
C | T | 1 | a0001c0001t0033g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1477-134G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109349 | ||||||
chr10:15109536
|
A | C | 15 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1476+166T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109536 | ||||||
chr10:15109574
|
A | T | 2 | a0001c0001t0009g0046a0001c0001t0009g0066 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1476+128T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109574 | ||||||
chr10:15109578
|
T | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(21): Show | 24 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1476+124A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109578 | ||||||
chr10:15109582
|
T | A | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1476+120A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109582 | ||||||
chr10:15109608
|
A | C | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1476+94T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109608 | ||||||
chr10:15109866
|
T | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1339-27A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109866 | ||||||
chr10:15109867
|
T | C | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-28A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109867 | ||||||
chr10:15109868
|
A | T | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-29T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109868 | ||||||
chr10:15109877
|
G | A | 9 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(6): Show | 9 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1339-38C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109877 | ||||||
chr10:15109908
|
T | G | 91 | a0001c0001t0001g0267a0001c0001t0003g0049a0001c0001t0003g0052others(88): Show | 91 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1339-69A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109908 | ||||||
chr10:15110007
|
C | T | 1 | a0001c0003t0008g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1339-168G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110007 | ||||||
chr10:15110141
|
C | G | 37 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0038others(34): Show | 37 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1339-302G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110141 | ||||||
chr10:15110235
|
G | T | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1339-396C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110235 | ||||||
chr10:15110251
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0161a0001c0001t0050g0239 | 3 | HG00639.hp2 HG01099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1339-412G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110251 | ||||||
chr10:15110381
|
A | G | 61 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(58): Show | 61 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1339-542T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110381 | ||||||
chr10:15110496
|
C | T | 5 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-657G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110496 | ||||||
chr10:15110534
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1339-695C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110534 | ||||||
chr10:15110560
|
G | C | 140 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(137): Show | 140 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.1339-721C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110560 | ||||||
chr10:15110606
|
A | C | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-767T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110606 | ||||||
chr10:15110624
|
A | C | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-785T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110624 | ||||||
chr10:15110642
|
C | A | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-803G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110642 | ||||||
chr10:15110643
|
A | C | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-804T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110643 | ||||||
chr10:15110646
|
C | CAAA | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1339-810_1339-808d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110646 | ||||||
chr10:15110662
|
C | A | 2 | a0001c0002t0031g0270a0001c0002t0032g0101 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1339-823G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110662 | ||||||
chr10:15110690
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1339-851G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110690 | ||||||
chr10:15110907
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0164a0001c0001t0001g0254 | 3 | HG00597.hp2 HG01952.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1339-1068G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110907 | ||||||
chr10:15110953
|
G | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(21): Show | 24 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1339-1114C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110953 | ||||||
chr10:15110972
|
T | C | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1339-1133A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110972 | ||||||
chr10:15111279
|
A | G | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1339-1440T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111279 | ||||||
chr10:15111319
|
G | A | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1338+1477C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111319 | ||||||
chr10:15111378
|
G | T | 25 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(22): Show | 25 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1338+1418C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111378 | ||||||
chr10:15111509
|
C | CA | 52 | a0001c0001t0001g0084a0001c0001t0001g0171a0001c0001t0001g0210others(49): Show | 52 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1338+1286dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111509 | ||||||
chr10:15111509
|
CA | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0252a0001c0001t0001g0259others(3): Show | 6 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+1286delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111509 | ||||||
chr10:15111513
|
A | G | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1338+1283T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111513 | ||||||
chr10:15111520
|
A | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(33): Show | 36 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1338+1276T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111520 | ||||||
chr10:15111656
|
G | A | 37 | a0001c0001t0001g0267a0001c0001t0003g0049a0001c0001t0003g0052others(34): Show | 37 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1338+1140C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111656 | ||||||
chr10:15111686
|
G | A | 5 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+1110C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111686 | ||||||
chr10:15111979
|
A | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1338+817T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111979 | ||||||
chr10:15112121
|
A | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1338+675T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112121 | ||||||
chr10:15112174
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1338+622A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
T | TTA | 7 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0135others(4): Show | 7 | HG01074.hp2 HG01433.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1338+620_1338+621d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
T | TTATA | 6 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0195others(3): Show | 6 | HG00140.hp1 HG00597.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+618_1338+621d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
T | TTATATA | 5 | a0001c0001t0001g0040a0001c0001t0001g0157a0001c0001t0001g0190others(2): Show | 5 | HG01517.hp2 HG01934.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+616_1338+621d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0265 | 2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1338+612_1338+621d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1338+610_1338+621d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1338+608_1338+621d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0011g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338+612_1338+621d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112174
|
TTATATAT others(5): Show |
T | 1 | a0001c0007t0011g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1338+610_1338+621d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | ||||||
chr10:15112192
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1338+576_1338+603d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112192 | ||||||
chr10:15112194
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0012g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1338+575_1338+601d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | ||||||
chr10:15112194
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0012g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1338+574_1338+601d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | ||||||
chr10:15112194
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0012g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1338+572_1338+601d others(32): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | ||||||
chr10:15112194
|
ATATATAT others(29): Show |
A | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1338+566_1338+601d others(38): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | ||||||
chr10:15112196
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1338+579_1338+599d others(23): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | ||||||
chr10:15112196
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0085a0001c0001t0001g0169 | 2 | NA18960.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1338+577_1338+599d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | ||||||
chr10:15112196
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1338+574_1338+599d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | ||||||
chr10:15112196
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0006g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1338+572_1338+599d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | ||||||
chr10:15112196
|
ATATATAT others(26): Show |
A | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1338+567_1338+599d others(35): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | ||||||
chr10:15112196
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1338+566_1338+599d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | ||||||
chr10:15112198
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0267 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1338+579_1338+597d others(21): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | ||||||
chr10:15112198
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0029 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1338+577_1338+597d others(23): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | ||||||
chr10:15112198
|
ATATATAT others(21): Show |
A | 6 | a0001c0001t0006g0048a0001c0001t0006g0108a0001c0001t0006g0109others(3): Show | 6 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+570_1338+597d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | ||||||
chr10:15112198
|
ATATATAT others(27): Show |
A | 4 | a0001c0001t0001g0026a0001c0001t0002g0063a0001c0001t0002g0158others(1): Show | 4 | HG01099.hp1 NA18959.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+564_1338+597d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | ||||||
chr10:15112198
|
ATATATAT others(29): Show |
A | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+562_1338+597d others(38): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | ||||||
chr10:15112200
|
ATATATAT others(13): Show |
A | 3 | a0001c0001t0001g0153a0001c0001t0001g0219a0001c0001t0001g0266 | 3 | HG02071.hp2 NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1338+576_1338+595d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1338+574_1338+595d others(24): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0006g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1338+570_1338+595d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(20): Show |
A | 1 | a0001c0002t0012g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1338+569_1338+595d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0006g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1338+568_1338+595d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0005g0205 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338+564_1338+595d others(34): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(26): Show |
A | 3 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0039g0021 | 3 | HG02071.hp1 HG03927.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1338+563_1338+595d others(35): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112200
|
ATATATAT others(27): Show |
A | 6 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0041others(3): Show | 6 | HG01081.hp1 HG02074.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+562_1338+595d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | ||||||
chr10:15112202
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1338+576_1338+593d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112202
|
ATATATAT others(17): Show |
A | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1338+570_1338+593d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112202
|
ATATATAT others(18): Show |
A | 1 | a0001c0004t0013g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1338+569_1338+593d others(27): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112202
|
ATATATAT others(19): Show |
A | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1338+568_1338+593d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112202
|
ATATATAT others(25): Show |
A | 6 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0037others(3): Show | 6 | HG00438.hp1 HG02155.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+562_1338+593d others(34): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112202
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1338+560_1338+593d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112202
|
ATATATAT others(31): Show |
A | 1 | a0001c0001t0024g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1338+556_1338+593d others(40): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | ||||||
chr10:15112204
|
ATATATAT others(6): Show |
A | 1 | a0001c0002t0014g0073 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1338+579_1338+591d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1338+578_1338+591d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0047g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1338+576_1338+591d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0009g0168a0001c0001t0009g0202 | 2 | HG00639.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1338+575_1338+591d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0052g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1338+574_1338+591d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1338+569_1338+591d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(19): Show |
A | 3 | a0001c0001t0013g0111a0001c0002t0013g0099a0001c0004t0013g0112 | 3 | HG02886.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1338+566_1338+591d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0005g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1338+563_1338+591d others(31): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112204
|
ATATATAT others(25): Show |
A | 2 | a0001c0001t0002g0042a0001c0002t0002g0142 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1338+560_1338+591d others(34): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | ||||||
chr10:15112205
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0011g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1338+580_1338+590d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112205 | ||||||
chr10:15112206
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0011g0007a0001c0001t0011g0122 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1338+579_1338+589d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | ||||||
chr10:15112206
|
ATATATAT others(5): Show |
A | 1 | a0001c0002t0014g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1338+578_1338+589d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | ||||||
chr10:15112206
|
ATATATAT others(6): Show |
A | 2 | a0001c0002t0014g0087a0001c0002t0014g0089 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1338+577_1338+589d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | ||||||
chr10:15112206
|
ATATATAT others(10): Show |
A | 4 | a0001c0001t0009g0003a0001c0001t0009g0097a0001c0001t0022g0086others(1): Show | 4 | HG00738.hp1 HG02083.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+573_1338+589d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | ||||||
chr10:15112206
|
ATATATAT others(16): Show |
A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1338+567_1338+589d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | ||||||
chr10:15112206
|
ATATATAT others(19): Show |
A | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1338+564_1338+589d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | ||||||
chr10:15112208
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0011g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+572_1338+587d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112208
|
ATATATAT others(11): Show |
A | 2 | a0001c0001t0009g0066a0001c0001t0022g0080 | 2 | HG01192.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1338+570_1338+587d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112208
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0033g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+566_1338+587d others(24): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112208
|
ATATATAT others(16): Show |
A | 3 | a0001c0002t0010g0011a0001c0002t0010g0012a0002c0008t0010g0013 | 3 | HG02647.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1338+565_1338+587d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112208
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1338+564_1338+587d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112208
|
ATATATAT others(20): Show |
A | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1338+561_1338+587d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112208
|
ATATATAT others(26): Show |
A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1338+555_1338+587d others(35): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | ||||||
chr10:15112210
|
ATATATAT others(1): Show |
A | 6 | a0001c0001t0004g0002a0001c0001t0004g0106a0001c0001t0004g0269others(3): Show | 6 | HG01243.hp1 HG02922.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+578_1338+585d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112210
|
ATATATAT others(2): Show |
A | 6 | a0001c0001t0001g0171a0001c0001t0001g0242a0001c0001t0001g0244others(3): Show | 6 | HG00735.hp2 HG01975.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+577_1338+585d others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112210
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1338+576_1338+585d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112210
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0051g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1338+573_1338+585d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112210
|
ATATATAT others(8): Show |
A | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1338+571_1338+585d others(17): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112210
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0009g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1338+570_1338+585d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112210
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0017g0228a0001c0001t0017g0258 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1338+566_1338+585d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | ||||||
chr10:15112211
|
TATATA | T | 3 | a0001c0001t0001g0165a0001c0001t0003g0071a0001c0001t0004g0119 | 3 | HG00597.hp1 HG00673.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1338+580_1338+584d others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112211 | ||||||
chr10:15112214
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1338+570_1338+581d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112214 | ||||||
chr10:15112214
|
ATATTTTT others(12): Show |
A | 1 | a0001c0001t0005g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1338+563_1338+581d others(21): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112214 | ||||||
chr10:15112216
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0233 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1338+579_1338+580i others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
A | T | 1 | a0001c0001t0011g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338+580T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
AT | A | 14 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0137others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+579delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATT | A | 10 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0134others(7): Show | 10 | HG00621.hp1 HG02027.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+578_1338+579d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATTT | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0035others(9): Show | 12 | HG00558.hp1 HG00738.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1338+577_1338+579d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATTTT | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0139a0001c0001t0001g0191others(4): Show | 7 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1338+576_1338+579d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATTTTT | A | 7 | a0001c0001t0001g0034a0001c0001t0001g0162a0001c0001t0001g0170others(4): Show | 7 | HG00621.hp2 NA18940.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338+575_1338+579d others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATTTTTTT | A | 5 | a0001c0001t0001g0212a0001c0001t0001g0216a0001c0001t0001g0234others(2): Show | 5 | HG01071.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+573_1338+579d others(9): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1338+570_1338+579d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112216
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0004t0025g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1338+566_1338+579d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | ||||||
chr10:15112217
|
T | TA | 10 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0083others(7): Show | 10 | HG00423.hp1 HG00423.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+578_1338+579i others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | ||||||
chr10:15112217
|
T | TATA | 3 | a0001c0001t0001g0194a0001c0001t0001g0226a0001c0001t0036g0243 | 3 | HG01074.hp1 HG02027.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1338+578_1338+579i others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | ||||||
chr10:15112217
|
T | TATATATA | 4 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0008g0147others(1): Show | 4 | HG00558.hp2 HG02129.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+578_1338+579i others(9): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | ||||||
chr10:15112217
|
T | TATATATA others(2): Show |
4 | a0001c0001t0001g0151a0001c0001t0001g0177a0001c0001t0001g0247others(1): Show | 4 | HG01258.hp2 HG02056.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+578_1338+579i others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | ||||||
chr10:15112218
|
T | A | 29 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0033others(26): Show | 29 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1338+578A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112218 | ||||||
chr10:15112219
|
T | A | 30 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0064others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1338+577A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112219 | ||||||
chr10:15112220
|
T | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0039others(24): Show | 27 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1338+576A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112220 | ||||||
chr10:15112221
|
T | A | 21 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0060others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1338+575A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112221 | ||||||
chr10:15112222
|
T | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0059others(11): Show | 14 | HG00597.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+574A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112222 | ||||||
chr10:15112223
|
T | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0075others(6): Show | 9 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338+573A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112223 | ||||||
chr10:15112224
|
T | A | 4 | a0001c0001t0001g0188a0001c0001t0053g0006a0001c0002t0005g0143others(1): Show | 4 | HG02622.hp2 HG02698.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+572A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112224 | ||||||
chr10:15112225
|
T | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0234a0001c0001t0026g0100 | 3 | HG01071.hp1 HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1338+571A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112225 | ||||||
chr10:15112226
|
T | A | 5 | a0001c0002t0005g0143a0001c0002t0005g0276a0001c0006t0016g0010others(2): Show | 5 | HG02622.hp2 HG02970.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+570A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112226 | ||||||
chr10:15112227
|
T | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0236a0001c0001t0005g0237others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+569A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112227 | ||||||
chr10:15112228
|
T | A | 7 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0002t0005g0143others(4): Show | 7 | HG02622.hp2 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338+568A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112228 | ||||||
chr10:15112229
|
T | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0236a0001c0001t0005g0237others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+567A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112229 | ||||||
chr10:15112230
|
T | A | 7 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0002t0005g0143others(4): Show | 7 | HG02622.hp2 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338+566A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112230 | ||||||
chr10:15112231
|
T | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0236a0001c0001t0005g0237others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+565A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112231 | ||||||
chr10:15112232
|
T | A | 8 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0002t0005g0143others(5): Show | 8 | HG01975.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1338+564A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112232 | ||||||
chr10:15112233
|
T | A | 3 | a0001c0001t0005g0207a0001c0001t0005g0236a0001c0001t0005g0237 | 3 | HG02055.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1338+563A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112233 | ||||||
chr10:15112234
|
T | A | 6 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0004t0025g0096others(3): Show | 6 | HG01975.hp2 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+562A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112234 | ||||||
chr10:15112235
|
T | A | 1 | a0001c0001t0005g0236 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1338+561A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112235 | ||||||
chr10:15112236
|
T | A | 1 | a0001c0004t0025g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1338+560A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112236 | ||||||
chr10:15112286
|
G | A | 2 | a0001c0001t0017g0228a0001c0001t0017g0258 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1338+510C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112286 | ||||||
chr10:15112321
|
C | G | 14 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+475G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112321 | ||||||
chr10:15112360
|
C | T | 14 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+436G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112360 | ||||||
chr10:15112398
|
T | G | 3 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238 | 3 | HG01891.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1338+398A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112398 | ||||||
chr10:15112420
|
G | C | 23 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(20): Show | 23 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1338+376C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112420 | ||||||
chr10:15112502
|
T | A | 39 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0038others(36): Show | 39 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1338+294A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112502 | ||||||
chr10:15112973
|
A | G | 1 | a0001c0001t0007g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1171-10T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15112973 | ||||||
chr10:15112975
|
A | G | 270 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(267): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1171-12T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15112975 | ||||||
chr10:15113003
|
C | T | 8 | a0001c0001t0011g0249a0001c0001t0023g0001a0001c0002t0014g0073others(5): Show | 8 | HG02280.hp1 HG02723.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1171-40G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113003 | ||||||
chr10:15113087
|
G | A | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1171-124C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113087 | ||||||
chr10:15113104
|
C | G | 15 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(12): Show | 15 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1171-141G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113104 | ||||||
chr10:15113296
|
C | T | 28 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(25): Show | 28 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1171-333G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113296 | ||||||
chr10:15113338
|
C | G | 22 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(19): Show | 22 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1171-375G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113338 | ||||||
chr10:15113463
|
C | CA | 51 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0058others(48): Show | 51 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1171-501dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAA | 33 | a0001c0001t0003g0071a0001c0001t0003g0233a0001c0001t0004g0274others(30): Show | 33 | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1171-502_1171-501d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAA | 11 | a0001c0001t0009g0066a0001c0001t0009g0097a0001c0001t0009g0202others(8): Show | 11 | HG01192.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1171-503_1171-501d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(6): Show |
1 | a0001c0004t0013g0112 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1171-513_1171-501d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0013g0111a0001c0001t0024g0074a0001c0002t0018g0271 | 3 | HG02145.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1171-514_1171-501d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0028g0118a0001c0002t0018g0268 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1171-516_1171-501d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0005g0005a0001c0001t0005g0205a0001c0001t0005g0257others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171-517_1171-501d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0005g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1171-518_1171-501d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1171-520_1171-501d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
C | CAAAAAAA others(27): Show |
1 | a0001c0004t0013g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1171-501_1171-500i others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
CA | C | 8 | a0001c0001t0001g0038a0001c0001t0001g0184a0001c0001t0001g0192others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.1171-501delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
CAAAAAAA others(1): Show |
C | 23 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(20): Show | 23 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1171-508_1171-501d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113463
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1171-514_1171-501d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | ||||||
chr10:15113486
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1171-524_1171-523i others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113486 | ||||||
chr10:15113486
|
A | G | 1 | a0001c0001t0021g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1171-523T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113486 | ||||||
chr10:15113549
|
G | A | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1171-586C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113549 | ||||||
chr10:15113567
|
G | T | 1 | a0001c0002t0002g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1171-604C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113567 | ||||||
chr10:15113626
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-663T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113626 | ||||||
chr10:15113627
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-664C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113627 | ||||||
chr10:15113630
|
C | G | 1 | a0001c0001t0002g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-667G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113630 | ||||||
chr10:15113632
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-669C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113632 | ||||||
chr10:15113633
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-670G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113633 | ||||||
chr10:15113695
|
T | G | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1171-732A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113695 | ||||||
chr10:15113748
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1171-785G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113748 | ||||||
chr10:15113924
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1171-961A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113924 | ||||||
chr10:15113927
|
C | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG00423.hp1 HG00558.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-964G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113927 | ||||||
chr10:15114360
|
A | G | 35 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(32): Show | 35 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.1171-1397T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114360 | ||||||
chr10:15114395
|
T | C | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1171-1432A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114395 | ||||||
chr10:15114457
|
C | G | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-1494G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114457 | ||||||
chr10:15114475
|
C | A | 71 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(68): Show | 71 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1171-1512G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114475 | ||||||
chr10:15114510
|
C | G | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-1547G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114510 | ||||||
chr10:15114532
|
C | G | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1171-1569G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114532 | ||||||
chr10:15114570
|
A | G | 38 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1171-1607T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114570 | ||||||
chr10:15114575
|
C | T | 38 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1171-1612G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114575 | ||||||
chr10:15114610
|
T | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(21): Show | 24 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1171-1647A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114610 | ||||||
chr10:15114676
|
C | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1171-1713G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114676 | ||||||
chr10:15114740
|
T | C | 70 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(67): Show | 70 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1171-1777A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114740 | ||||||
chr10:15114776
|
G | C | 41 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0038others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1171-1813C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114776 | ||||||
chr10:15114868
|
T | A | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1171-1905A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114868 | ||||||
chr10:15114934
|
G | A | 1 | a0001c0001t0017g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1171-1971C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114934 | ||||||
chr10:15115629
|
A | G | 2 | a0001c0001t0002g0063a0001c0001t0037g0179 | 2 | NA18980.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1171-2666T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115629 | ||||||
chr10:15115660
|
G | C | 1 | a0001c0001t0036g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1171-2697C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115660 | ||||||
chr10:15115726
|
C | G | 37 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(34): Show | 37 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1171-2763G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115726 | ||||||
chr10:15115772
|
A | G | 57 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(54): Show | 57 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.1171-2809T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115772 | ||||||
chr10:15115904
|
G | A | 6 | a0001c0001t0033g0107a0001c0002t0010g0011a0001c0002t0010g0012others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-2941C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115904 | ||||||
chr10:15115925
|
G | A | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1171-2962C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115925 | ||||||
chr10:15115968
|
C | T | 1 | a0001c0001t0044g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1171-3005G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115968 | ||||||
chr10:15116051
|
G | A | 11 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1171-3088C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116051 | ||||||
chr10:15116069
|
A | G | 106 | a0001c0001t0001g0064a0001c0001t0001g0139a0001c0001t0001g0267others(103): Show | 106 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1171-3106T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116069 | ||||||
chr10:15116084
|
G | C | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171-3121C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116084 | ||||||
chr10:15116088
|
T | C | 38 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1171-3125A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116088 | ||||||
chr10:15116123
|
G | T | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-3160C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116123 | ||||||
chr10:15116130
|
C | T | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1171-3167G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116130 | ||||||
chr10:15116243
|
A | T | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+3100T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116243 | ||||||
chr10:15116268
|
T | C | 53 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(50): Show | 53 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1170+3075A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116268 | ||||||
chr10:15116271
|
G | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0038others(1): Show | 4 | NA18940.hp2 NA18960.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+3072C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116271 | ||||||
chr10:15116310
|
A | G | 129 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(126): Show | 129 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1170+3033T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116310 | ||||||
chr10:15116369
|
A | G | 80 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(77): Show | 80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1170+2974T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116369 | ||||||
chr10:15116386
|
C | T | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+2957G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116386 | ||||||
chr10:15116409
|
C | T | 63 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(60): Show | 63 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1170+2934G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116409 | ||||||
chr10:15116444
|
C | T | 28 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(25): Show | 28 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1170+2899G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116444 | ||||||
chr10:15116635
|
C | A | 1 | a0001c0001t0003g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1170+2708G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116635 | ||||||
chr10:15116687
|
C | T | 35 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(32): Show | 35 | HG00140.hp2 HG00642.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1170+2656G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116687 | ||||||
chr10:15116701
|
A | G | 2 | a0001c0001t0009g0046a0001c0001t0009g0066 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1170+2642T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116701 | ||||||
chr10:15116729
|
G | C | 11 | a0001c0001t0026g0100a0001c0002t0010g0011a0001c0002t0010g0012others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+2614C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116729 | ||||||
chr10:15116755
|
G | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0258 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1170+2588C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116755 | ||||||
chr10:15116785
|
G | GAAC | 95 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(92): Show | 95 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1170+2555_1170+255 others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116785 | ||||||
chr10:15116826
|
T | C | 4 | a0001c0004t0025g0096a0001c0006t0016g0010a0001c0006t0016g0014others(1): Show | 4 | HG01975.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+2517A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116826 | ||||||
chr10:15117024
|
T | C | 19 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(16): Show | 19 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1170+2319A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117024 | ||||||
chr10:15117124
|
T | C | 29 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(26): Show | 29 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1170+2219A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117124 | ||||||
chr10:15117219
|
T | C | 20 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(17): Show | 20 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1170+2124A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117219 | ||||||
chr10:15117246
|
G | A | 1 | a0001c0001t0054g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1170+2097C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117246 | ||||||
chr10:15117303
|
T | C | 1 | a0001c0004t0013g0112 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1170+2040A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117303 | ||||||
chr10:15117497
|
A | T | 32 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1170+1846T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117497 | ||||||
chr10:15117635
|
T | C | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+1708A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117635 | ||||||
chr10:15117652
|
C | G | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1170+1691G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117652 | ||||||
chr10:15117699
|
G | C | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+1644C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117699 | ||||||
chr10:15117706
|
AAC | A | 37 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(34): Show | 37 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1170+1635_1170+163 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117706 | ||||||
chr10:15117710
|
C | T | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+1633G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117710 | ||||||
chr10:15117792
|
A | T | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1170+1551T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117792 | ||||||
chr10:15117884
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0245 | 3 | HG02809.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1170+1459G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117884 | ||||||
chr10:15118186
|
A | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+1157T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118186 | ||||||
chr10:15118193
|
A | G | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+1150T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118193 | ||||||
chr10:15118194
|
G | A | 15 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170+1149C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118194 | ||||||
chr10:15118200
|
C | G | 1 | a0001c0001t0012g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1170+1143G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118200 | ||||||
chr10:15118276
|
A | G | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1170+1067T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118276 | ||||||
chr10:15118319
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1170+1024G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118319 | ||||||
chr10:15118367
|
C | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1170+976G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118367 | ||||||
chr10:15118408
|
G | A | 15 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170+935C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118408 | ||||||
chr10:15118412
|
G | A | 5 | a0001c0001t0001g0155a0001c0002t0014g0073a0001c0002t0014g0087others(2): Show | 5 | HG01123.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170+931C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118412 | ||||||
chr10:15118484
|
A | T | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+859T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118484 | ||||||
chr10:15118504
|
A | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+839T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118504 | ||||||
chr10:15118589
|
C | CA | 45 | a0001c0001t0001g0064a0001c0001t0001g0226a0001c0001t0001g0267others(42): Show | 45 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1170+753dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118589 | ||||||
chr10:15118758
|
C | G | 6 | a0001c0001t0012g0077a0001c0001t0012g0078a0001c0001t0012g0079others(3): Show | 6 | HG00140.hp2 HG01261.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+585G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118758 | ||||||
chr10:15118786
|
G | C | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1170+557C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118786 | ||||||
chr10:15118960
|
G | T | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1170+383C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118960 | ||||||
chr10:15119030
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0049g0206 | 2 | HG03139.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1170+313G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119030 | ||||||
chr10:15119063
|
G | C | 10 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+280C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119063 | ||||||
chr10:15119125
|
C | T | 6 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(3): Show | 6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+218G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119125 | ||||||
chr10:15119263
|
T | C | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1170+80A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119263 | ||||||
chr10:15119275
|
A | C | 81 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(78): Show | 81 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1170+68T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119275 | ||||||
chr10:15119335
|
G | T | 22 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(19): Show | 22 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.1170+8C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119335 | ||||||
chr10:15119518
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | splice_region_variant&intron_variant | LOW | c.1000-5A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119518 | ||||||
chr10:15119672
|
G | A | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-159C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119672 | ||||||
chr10:15119697
|
T | G | 7 | a0001c0001t0004g0103a0001c0001t0004g0104a0001c0001t0004g0105others(4): Show | 7 | HG01243.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-184A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119697 | ||||||
chr10:15119855
|
C | T | 14 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-342G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119855 | ||||||
chr10:15119879
|
G | A | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1000-366C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119879 | ||||||
chr10:15119884
|
T | C | 4 | a0001c0001t0013g0111a0001c0002t0013g0099a0001c0004t0013g0112others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-371A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119884 | ||||||
chr10:15119959
|
C | G | 1 | a0001c0001t0006g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1000-446G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119959 | ||||||
chr10:15119964
|
C | T | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1000-451G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119964 | ||||||
chr10:15119965
|
G | A | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-452C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119965 | ||||||
chr10:15120062
|
G | A | 17 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1000-549C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120062 | ||||||
chr10:15120106
|
A | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-593T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120106 | ||||||
chr10:15120127
|
T | C | 9 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(6): Show | 9 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000-614A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120127 | ||||||
chr10:15120230
|
G | A | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1000-717C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120230 | ||||||
chr10:15120273
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1000-760G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120273 | ||||||
chr10:15120294
|
C | T | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000-781G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120294 | ||||||
chr10:15120295
|
G | A | 6 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(3): Show | 6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-782C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120295 | ||||||
chr10:15120306
|
A | G | 1 | a0001c0001t0024g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1000-793T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120306 | ||||||
chr10:15120319
|
G | A | 14 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-806C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120319 | ||||||
chr10:15120384
|
G | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1000-871C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120384 | ||||||
chr10:15120720
|
T | G | 1 | a0001c0002t0012g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1000-1207A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120720 | ||||||
chr10:15120739
|
G | A | 19 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(16): Show | 19 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1000-1226C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120739 | ||||||
chr10:15120756
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1000-1243C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120756 | ||||||
chr10:15120835
|
C | T | 18 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(15): Show | 18 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000-1322G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120835 | ||||||
chr10:15120856
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1000-1343C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120856 | ||||||
chr10:15120928
|
C | T | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-1415G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120928 | ||||||
chr10:15120970
|
A | C | 2 | a0001c0001t0017g0228a0001c0001t0017g0258 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1000-1457T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120970 | ||||||
chr10:15120978
|
G | C | 4 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(1): Show | 4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-1465C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120978 | ||||||
chr10:15121027
|
T | G | 6 | a0001c0001t0013g0111a0001c0001t0024g0074a0001c0001t0028g0118others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-1514A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121027 | ||||||
chr10:15121055
|
C | G | 3 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124 | 3 | HG01109.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1000-1542G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121055 | ||||||
chr10:15121056
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1000-1543T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121056 | ||||||
chr10:15121076
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0220 | 2 | HG01433.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1000-1563G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121076 | ||||||
chr10:15121154
|
T | C | 4 | a0001c0001t0001g0140a0001c0001t0001g0164a0001c0001t0001g0254others(1): Show | 4 | HG00597.hp2 HG01952.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-1641A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121154 | ||||||
chr10:15121199
|
T | A | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1000-1686A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121199 | ||||||
chr10:15121228
|
T | C | 6 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-1715A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121228 | ||||||
chr10:15121292
|
T | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1000-1779A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121292 | ||||||
chr10:15121301
|
G | T | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1788C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121301 | ||||||
chr10:15121363
|
G | C | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1850C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121363 | ||||||
chr10:15121510
|
G | A | 14 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-1997C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121510 | ||||||
chr10:15121613
|
C | T | 6 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(3): Show | 6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-2100G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121613 | ||||||
chr10:15122042
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1000-2529C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122042 | ||||||
chr10:15122080
|
T | A | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-2567A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122080 | ||||||
chr10:15122127
|
A | C | 6 | a0001c0001t0033g0107a0001c0002t0010g0011a0001c0002t0010g0012others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-2614T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122127 | ||||||
chr10:15122134
|
C | T | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1000-2621G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122134 | ||||||
chr10:15122458
|
C | T | 13 | a0001c0001t0001g0075a0001c0001t0001g0141a0001c0001t0001g0171others(10): Show | 13 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000-2945G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122458 | ||||||
chr10:15122464
|
C | T | 1 | a0001c0001t0046g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1000-2951G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122464 | ||||||
chr10:15122493
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000-2980G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122493 | ||||||
chr10:15122511
|
G | A | 2 | a0001c0001t0024g0074a0001c0001t0028g0118 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1000-2998C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122511 | ||||||
chr10:15122678
|
C | T | 5 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-3165G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122678 | ||||||
chr10:15122689
|
G | T | 23 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(20): Show | 23 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1000-3176C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122689 | ||||||
chr10:15122884
|
C | A | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1000-3371G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122884 | ||||||
chr10:15122933
|
T | TAA | 16 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(13): Show | 16 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1000-3422_1000-342 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122933 | ||||||
chr10:15122933
|
TA | T | 6 | a0001c0001t0001g0091a0001c0002t0010g0011a0001c0002t0010g0012others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-3421delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122933 | ||||||
chr10:15123161
|
C | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000-3648G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123161 | ||||||
chr10:15123186
|
A | C | 4 | a0001c0004t0025g0096a0001c0006t0016g0010a0001c0006t0016g0014others(1): Show | 4 | HG01975.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-3673T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123186 | ||||||
chr10:15123473
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1000-3960C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123473 | ||||||
chr10:15123502
|
C | T | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-3989G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123502 | ||||||
chr10:15123514
|
C | T | 4 | a0001c0004t0025g0096a0001c0006t0016g0010a0001c0006t0016g0014others(1): Show | 4 | HG01975.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-4001G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123514 | ||||||
chr10:15123531
|
G | GA | 15 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0084others(12): Show | 15 | HG01261.hp1 HG01361.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1000-4019dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123531 | ||||||
chr10:15123531
|
GA | G | 30 | a0001c0001t0001g0141a0001c0001t0003g0049a0001c0001t0003g0072others(27): Show | 30 | HG00140.hp2 HG00621.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000-4019delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123531 | ||||||
chr10:15123531
|
GAA | G | 33 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0052others(30): Show | 33 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1000-4020_1000-401 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123531 | ||||||
chr10:15123616
|
C | G | 134 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(131): Show | 134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1000-4103G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123616 | ||||||
chr10:15123705
|
T | C | 51 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1000-4192A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123705 | ||||||
chr10:15123800
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1000-4287A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123800 | ||||||
chr10:15123850
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0240 | 2 | NA18952.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1000-4337A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123850 | ||||||
chr10:15124034
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.999+4316T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124034 | ||||||
chr10:15124177
|
C | A | 10 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.999+4173G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124177 | ||||||
chr10:15124179
|
C | A | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.999+4171G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124179 | ||||||
chr10:15124556
|
C | T | 106 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(103): Show | 106 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.999+3794G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124556 | ||||||
chr10:15124564
|
A | G | 7 | a0001c0001t0005g0205a0001c0001t0005g0207a0001c0001t0005g0236others(4): Show | 7 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+3786T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124564 | ||||||
chr10:15124568
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.999+3782C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124568 | ||||||
chr10:15124635
|
C | T | 1 | a0001c0002t0010g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.999+3715G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124635 | ||||||
chr10:15124722
|
C | A | 4 | a0001c0001t0009g0003a0001c0001t0009g0168a0001c0001t0009g0202others(1): Show | 4 | HG00639.hp1 HG00738.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+3628G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124722 | ||||||
chr10:15124726
|
G | A | 104 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(101): Show | 104 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.999+3624C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124726 | ||||||
chr10:15124906
|
A | G | 132 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0043others(129): Show | 132 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.999+3444T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124906 | ||||||
chr10:15124923
|
A | G | 11 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0108others(8): Show | 11 | HG00642.hp1 HG01109.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.999+3427T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124923 | ||||||
chr10:15125001
|
TG | T | 4 | a0001c0001t0004g0119a0001c0002t0013g0099a0001c0004t0013g0112others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+3348delC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125001 | ||||||
chr10:15125107
|
C | T | 10 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+3243G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125107 | ||||||
chr10:15125278
|
G | C | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.999+3072C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125278 | ||||||
chr10:15125294
|
A | G | 5 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3056T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125294 | ||||||
chr10:15125308
|
A | C | 41 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0003g0049others(38): Show | 41 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.999+3042T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125308 | ||||||
chr10:15125452
|
A | G | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.999+2898T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125452 | ||||||
chr10:15125512
|
G | C | 6 | a0001c0001t0049g0206a0001c0002t0010g0011a0001c0002t0010g0012others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+2838C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125512 | ||||||
chr10:15125628
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.999+2722A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125628 | ||||||
chr10:15125628
|
T | TTGTA | 7 | a0001c0001t0001g0141a0001c0001t0001g0171a0001c0001t0001g0242others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+2718_999+2721d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125628 | ||||||
chr10:15125658
|
GTATTTAG others(5): Show |
G | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.999+2680_999+2691d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125658 | ||||||
chr10:15125698
|
C | T | 6 | a0001c0002t0005g0276a0001c0002t0014g0073a0001c0002t0014g0087others(3): Show | 6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+2652G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125698 | ||||||
chr10:15125801
|
G | A | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.999+2549C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125801 | ||||||
chr10:15125911
|
C | T | 3 | a0001c0001t0049g0206a0001c0002t0031g0270a0001c0002t0032g0101 | 3 | HG02615.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.999+2439G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125911 | ||||||
chr10:15125916
|
T | C | 11 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.999+2434A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125916 | ||||||
chr10:15125944
|
T | C | 92 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(89): Show | 92 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.999+2406A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125944 | ||||||
chr10:15125955
|
G | A | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.999+2395C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125955 | ||||||
chr10:15125955
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.999+2395C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125955 | ||||||
chr10:15125960
|
T | C | 1 | a0001c0002t0019g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.999+2390A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125960 | ||||||
chr10:15125964
|
C | T | 1 | a0001c0002t0018g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.999+2386G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125964 | ||||||
chr10:15126008
|
A | G | 2 | a0001c0002t0010g0090a0001c0002t0018g0271 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.999+2342T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126008 | ||||||
chr10:15126024
|
A | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(14): Show | 17 | HG00438.hp1 HG00609.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.999+2326T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126024 | ||||||
chr10:15126041
|
GC | G | 7 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0002t0010g0090others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+2308delG | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126041 | ||||||
chr10:15126154
|
C | T | 1 | a0001c0001t0009g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.999+2196G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126154 | ||||||
chr10:15126155
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0151 | 2 | HG01258.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.999+2195C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126155 | ||||||
chr10:15126244
|
T | C | 29 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+2106A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126244 | ||||||
chr10:15126325
|
A | G | 2 | a0001c0001t0009g0003a0001c0001t0009g0168 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.999+2025T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126325 | ||||||
chr10:15126338
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.999+2012T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126338 | ||||||
chr10:15126428
|
T | TA | 53 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0031others(50): Show | 53 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+1921dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126428 | ||||||
chr10:15126428
|
TA | T | 20 | a0001c0001t0001g0025a0001c0001t0001g0149a0001c0001t0001g0191others(17): Show | 20 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+1921delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126428 | ||||||
chr10:15126460
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0138 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.999+1890C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126460 | ||||||
chr10:15126494
|
G | C | 2 | a0001c0002t0002g0017a0001c0002t0012g0018 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.999+1856C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126494 | ||||||
chr10:15126560
|
T | C | 94 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(91): Show | 94 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.999+1790A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126560 | ||||||
chr10:15126711
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.999+1639A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126711 | ||||||
chr10:15126821
|
A | G | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.999+1529T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126821 | ||||||
chr10:15126957
|
G | A | 29 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(26): Show | 29 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.999+1393C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126957 | ||||||
chr10:15127007
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0171a0001c0001t0001g0242others(1): Show | 4 | HG00735.hp2 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+1343G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127007 | ||||||
chr10:15127048
|
T | C | 63 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(60): Show | 63 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.999+1302A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127048 | ||||||
chr10:15127164
|
G | A | 5 | a0001c0002t0013g0099a0001c0004t0013g0112a0001c0004t0013g0113others(2): Show | 5 | HG01975.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+1186C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127164 | ||||||
chr10:15127241
|
T | A | 4 | a0001c0001t0012g0077a0001c0001t0012g0078a0001c0001t0012g0079others(1): Show | 4 | HG00140.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+1109A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127241 | ||||||
chr10:15127246
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.999+1104T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127246 | ||||||
chr10:15127249
|
T | TA | 6 | a0001c0001t0001g0020a0001c0002t0010g0011a0001c0002t0010g0012others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+1100dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127249 | ||||||
chr10:15127314
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999+1036C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127314 | ||||||
chr10:15127375
|
G | A | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.999+975C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127375 | ||||||
chr10:15127416
|
G | A | 1 | a0001c0001t0004g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.999+934C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127416 | ||||||
chr10:15127427
|
G | C | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.999+923C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127427 | ||||||
chr10:15127482
|
G | A | 28 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(25): Show | 28 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.999+868C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127482 | ||||||
chr10:15127493
|
G | A | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+857C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127493 | ||||||
chr10:15127502
|
C | A | 20 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(17): Show | 20 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+848G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127502 | ||||||
chr10:15127502
|
C | G | 44 | a0001c0001t0004g0119a0001c0001t0009g0003a0001c0001t0009g0046others(41): Show | 44 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.999+848G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127502 | ||||||
chr10:15127503
|
C | T | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.999+847G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127503 | ||||||
chr10:15127508
|
C | A | 20 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(17): Show | 20 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+842G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127508 | ||||||
chr10:15127525
|
C | T | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+825G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127525 | ||||||
chr10:15127530
|
G | C | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+820C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127530 | ||||||
chr10:15127533
|
T | C | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+817A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127533 | ||||||
chr10:15127538
|
C | T | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+812G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127538 | ||||||
chr10:15127542
|
G | A | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+808C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127542 | ||||||
chr10:15127546
|
C | CA | 55 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0032others(52): Show | 55 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.999+803dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127546 | ||||||
chr10:15127546
|
C | CAA | 13 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0093others(10): Show | 13 | HG00673.hp2 HG00735.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.999+802_999+803dup others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127546 | ||||||
chr10:15127548
|
A | G | 1 | a0001c0003t0008g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.999+802T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127548 | ||||||
chr10:15127556
|
A | T | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+794T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127556 | ||||||
chr10:15127557
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.999+779_999+792del others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127557 | ||||||
chr10:15127557
|
AAAAAAAA others(23): Show |
A | 65 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+763_999+792del others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127557 | ||||||
chr10:15127560
|
A | AT | 29 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+789_999+790ins others(1): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127560 | ||||||
chr10:15127562
|
A | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 6 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+788T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127562 | ||||||
chr10:15127563
|
A | AAT | 7 | a0001c0001t0006g0108a0001c0001t0006g0110a0001c0001t0006g0115others(4): Show | 7 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+786_999+787ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127563 | ||||||
chr10:15127563
|
A | T | 2 | a0001c0001t0001g0058a0001c0001t0007g0156 | 2 | HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.999+787T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127563 | ||||||
chr10:15127565
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.999+785T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127565 | ||||||
chr10:15127567
|
A | T | 1 | a0001c0001t0007g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.999+783T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127567 | ||||||
chr10:15127570
|
A | T | 2 | a0001c0001t0001g0193a0001c0001t0006g0109 | 2 | HG02083.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.999+780T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127570 | ||||||
chr10:15127570
|
AT | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0140a0001c0001t0001g0184others(3): Show | 6 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+779delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127570 | ||||||
chr10:15127571
|
T | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0030others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.999+779A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127571 | ||||||
chr10:15127575
|
T | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0032others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.999+775A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127575 | ||||||
chr10:15127578
|
A | AAAAAATA others(4): Show |
4 | a0001c0001t0005g0203a0001c0001t0011g0007a0001c0001t0011g0009others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+771_999+772ins others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | ||||||
chr10:15127578
|
A | AAT | 8 | a0001c0001t0006g0048a0001c0001t0006g0081a0001c0001t0006g0109others(5): Show | 8 | HG01975.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+771_999+772ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | ||||||
chr10:15127578
|
A | AATAAAAT | 7 | a0001c0001t0006g0108a0001c0001t0006g0110a0001c0001t0006g0115others(4): Show | 7 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+771_999+772ins others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | ||||||
chr10:15127578
|
A | T | 3 | a0001c0001t0011g0122a0001c0001t0011g0249a0001c0001t0044g0116 | 3 | HG02486.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.999+772T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | ||||||
chr10:15127579
|
T | A | 50 | a0001c0001t0001g0033a0001c0001t0001g0141a0001c0001t0001g0144others(47): Show | 50 | HG00642.hp1 HG00735.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.999+771A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127579 | ||||||
chr10:15127582
|
A | T | 6 | a0001c0001t0005g0204a0001c0001t0005g0205a0001c0001t0005g0236others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+768T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127582 | ||||||
chr10:15127582
|
AT | A | 29 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+767delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127582 | ||||||
chr10:15127583
|
T | A | 7 | a0001c0001t0005g0204a0001c0001t0005g0205a0001c0001t0005g0236others(4): Show | 7 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+767A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127583 | ||||||
chr10:15127586
|
A | AAT | 20 | a0001c0001t0005g0203a0001c0001t0006g0048a0001c0001t0006g0081others(17): Show | 20 | HG00642.hp1 HG01975.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+763_999+764ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127586 | ||||||
chr10:15127586
|
A | AATAAAAT others(5): Show |
8 | a0001c0001t0005g0005a0001c0001t0005g0207a0001c0001t0005g0257others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+763_999+764ins others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127586 | ||||||
chr10:15127586
|
A | T | 29 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+764T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127586 | ||||||
chr10:15127587
|
T | A | 57 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(54): Show | 57 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.999+763A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127587 | ||||||
chr10:15127587
|
T | TAAAATAA others(4): Show |
6 | a0001c0001t0005g0204a0001c0001t0005g0205a0001c0001t0005g0236others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+762_999+763ins others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127587 | ||||||
chr10:15127591
|
T | TA | 3 | a0001c0001t0001g0140a0001c0001t0001g0164a0001c0001t0001g0254 | 3 | HG00597.hp2 HG01952.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.999+758dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127591 | ||||||
chr10:15127760
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999+590C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127760 | ||||||
chr10:15127788
|
AGCTACTT others(22): Show |
A | 1 | a0001c0001t0035g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.999+533_999+561del others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127788 | ||||||
chr10:15127794
|
T | A | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.999+556A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127794 | ||||||
chr10:15127867
|
C | T | 5 | a0001c0002t0013g0099a0001c0004t0013g0112a0001c0004t0013g0113others(2): Show | 5 | HG01975.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+483G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127867 | ||||||
chr10:15127896
|
TC | T | 53 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(50): Show | 53 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.999+453delG | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127896 | ||||||
chr10:15127898
|
CA | C | 44 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(41): Show | 44 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.999+451delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127898 | ||||||
chr10:15127898
|
CAA | C | 6 | a0001c0002t0005g0143a0001c0002t0015g0102a0001c0002t0015g0123others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.999+450_999+451del others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127898 | ||||||
chr10:15127899
|
A | T | 53 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(50): Show | 53 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.999+451T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127899 | ||||||
chr10:15128162
|
G | A | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+188C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128162 | ||||||
chr10:15128163
|
G | A | 6 | a0001c0002t0005g0143a0001c0002t0015g0102a0001c0002t0015g0123others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.999+187C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128163 | ||||||
chr10:15128209
|
G | A | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+141C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128209 | ||||||
chr10:15128243
|
T | C | 5 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+107A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128243 | ||||||
chr10:15129059
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.891-601C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129059 | ||||||
chr10:15129154
|
C | A | 2 | a0001c0001t0024g0074a0001c0001t0028g0118 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.891-696G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129154 | ||||||
chr10:15129269
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.891-811C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129269 | ||||||
chr10:15129721
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0155 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.890+421G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129721 | ||||||
chr10:15129841
|
G | A | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.890+301C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129841 | ||||||
chr10:15129894
|
T | C | 41 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.890+248A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129894 | ||||||
chr10:15129907
|
C | CA | 64 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0031others(61): Show | 64 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.890+234dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129907 | ||||||
chr10:15129907
|
C | CAA | 9 | a0001c0001t0001g0029a0001c0001t0005g0205a0001c0001t0005g0207others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.890+233_890+234dup others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129907 | ||||||
chr10:15129907
|
CA | C | 15 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0221others(12): Show | 15 | HG00673.hp1 HG01081.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.890+234delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129907 | ||||||
chr10:15129908
|
A | T | 1 | a0001c0001t0001g0153 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.890+234T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129908 | ||||||
chr10:15129933
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.890+209A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129933 | ||||||
chr10:15130094
|
A | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0053others(5): Show | 8 | HG00423.hp1 HG00558.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.890+48T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15130094 | ||||||
chr10:15130445
|
G | A | 42 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(39): Show | 42 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.720-133C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130445 | ||||||
chr10:15130549
|
C | CAG | 66 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(63): Show | 66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.720-238_720-237ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130549 | ||||||
chr10:15130679
|
G | C | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.720-367C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130679 | ||||||
chr10:15130703
|
C | CA | 67 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0069others(64): Show | 67 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.720-392dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | ||||||
chr10:15130703
|
C | CAA | 24 | a0001c0001t0001g0026a0001c0001t0002g0023a0001c0001t0002g0027others(21): Show | 24 | HG01099.hp1 HG01192.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.720-393_720-392dup others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | ||||||
chr10:15130703
|
C | CAAA | 13 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0031others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.720-394_720-392dup others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | ||||||
chr10:15130703
|
CA | C | 9 | a0001c0001t0008g0092a0001c0001t0012g0077a0001c0001t0012g0079others(6): Show | 9 | HG00140.hp2 HG00438.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.720-392delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | ||||||
chr10:15130756
|
A | G | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.720-444T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130756 | ||||||
chr10:15130786
|
C | CT | 19 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0059others(16): Show | 19 | HG01074.hp2 HG02027.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.720-475dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130786 | ||||||
chr10:15130786
|
CT | C | 13 | a0001c0001t0009g0168a0001c0001t0022g0080a0001c0001t0035g0114others(10): Show | 13 | HG00639.hp1 HG01192.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.720-475delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130786 | ||||||
chr10:15130786
|
CTT | C | 7 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(4): Show | 7 | HG00738.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.720-476_720-475del others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130786 | ||||||
chr10:15130790
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.720-478A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130790 | ||||||
chr10:15130876
|
T | G | 66 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(63): Show | 66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.720-564A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130876 | ||||||
chr10:15130879
|
T | C | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720-567A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130879 | ||||||
chr10:15130892
|
C | T | 2 | a0001c0001t0020g0065a0001c0001t0020g0068 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.720-580G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130892 | ||||||
chr10:15130983
|
T | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0138 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.720-671A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130983 | ||||||
chr10:15131000
|
C | T | 5 | a0001c0001t0012g0077a0001c0001t0012g0078a0001c0001t0012g0079others(2): Show | 5 | HG00140.hp2 HG01261.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.720-688G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131000 | ||||||
chr10:15131009
|
C | T | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.720-697G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131009 | ||||||
chr10:15131067
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0069 | 3 | HG00099.hp1 HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.720-755G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131067 | ||||||
chr10:15131157
|
A | C | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.720-845T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131157 | ||||||
chr10:15131209
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0245others(1): Show | 4 | HG01175.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-897G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131209 | ||||||
chr10:15131257
|
A | G | 36 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(33): Show | 36 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.720-945T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131257 | ||||||
chr10:15131287
|
A | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0245others(1): Show | 4 | HG01175.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-975T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131287 | ||||||
chr10:15131312
|
C | CT | 6 | a0001c0001t0001g0135a0001c0001t0001g0153a0001c0001t0001g0175others(3): Show | 6 | HG01109.hp2 HG02970.hp1 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.720-1001dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131312 | ||||||
chr10:15131348
|
G | A | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720-1036C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131348 | ||||||
chr10:15131440
|
C | T | 2 | a0001c0001t0017g0228a0001c0001t0017g0258 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.720-1128G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131440 | ||||||
chr10:15131450
|
G | A | 1 | a0001c0002t0014g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.720-1138C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131450 | ||||||
chr10:15131506
|
G | C | 2 | a0001c0001t0017g0228a0001c0001t0017g0258 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.720-1194C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131506 | ||||||
chr10:15131560
|
C | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0038g0183 | 3 | HG01123.hp1 HG02735.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.720-1248G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131560 | ||||||
chr10:15131742
|
G | T | 7 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238others(4): Show | 7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.719+1075C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131742 | ||||||
chr10:15131832
|
G | A | 3 | a0001c0005t0003g0125a0001c0005t0003g0129a0001c0005t0009g0128 | 3 | HG03098.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.719+985C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131832 | ||||||
chr10:15131876
|
T | G | 2 | a0001c0001t0011g0249a0001c0001t0044g0116 | 2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.719+941A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131876 | ||||||
chr10:15131976
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.719+841C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131976 | ||||||
chr10:15132170
|
G | T | 27 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(24): Show | 27 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.719+647C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132170 | ||||||
chr10:15132231
|
A | G | 1 | a0001c0001t0005g0237 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.719+586T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132231 | ||||||
chr10:15132276
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.719+541C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132276 | ||||||
chr10:15132276
|
GT | G | 21 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.719+540delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132276 | ||||||
chr10:15132489
|
G | A | 27 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.719+328C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132489 | ||||||
chr10:15132633
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.719+184C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132633 | ||||||
chr10:15132720
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.719+97C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132720 | ||||||
chr10:15132780
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.719+37T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132780 | ||||||
chr10:15132793
|
G | A | 2 | a0001c0001t0009g0097a0001c0001t0052g0067 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.719+24C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132793 | ||||||
chr10:15132810
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0033g0107 | 2 | HG00642.hp1 HG02109.hp1 |
splice_region_variant&intron_variant | LOW | c.719+7G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132810 | ||||||
chr10:15133008
|
A | G | 1 | a0001c0001t0041g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.602+45T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 5/11 | chr10 | 15133008 | ||||||
chr10:15133013
|
G | A | 7 | a0001c0002t0005g0143a0001c0002t0013g0099a0001c0002t0015g0102others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.602+40C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 5/11 | chr10 | 15133013 | ||||||
chr10:15133206
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.510+39T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 4/11 | chr10 | 15133206 | ||||||
chr10:15133435
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.392-72A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133435 | ||||||
chr10:15133459
|
A | C | 7 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238others(4): Show | 7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-96T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133459 | ||||||
chr10:15133579
|
A | G | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.392-216T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133579 | ||||||
chr10:15133609
|
C | T | 23 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(20): Show | 23 | HG00642.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.392-246G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133609 | ||||||
chr10:15133622
|
T | G | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0200others(3): Show | 6 | HG01943.hp1 HG01952.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-259A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133622 | ||||||
chr10:15133627
|
C | T | 5 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-264G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133627 | ||||||
chr10:15133671
|
T | C | 66 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(63): Show | 66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.392-308A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133671 | ||||||
chr10:15133782
|
C | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0241a0001c0001t0036g0243 | 3 | HG02027.hp2 HG02135.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.392-419G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133782 | ||||||
chr10:15133837
|
C | G | 4 | a0001c0001t0012g0077a0001c0001t0012g0078a0001c0001t0012g0079others(1): Show | 4 | HG00140.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-474G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133837 | ||||||
chr10:15133857
|
G | C | 7 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238others(4): Show | 7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-494C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133857 | ||||||
chr10:15134158
|
A | G | 128 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(125): Show | 128 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.392-795T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134158 | ||||||
chr10:15134297
|
C | T | 6 | a0001c0002t0005g0143a0001c0002t0015g0102a0001c0002t0015g0123others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-934G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134297 | ||||||
chr10:15134324
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.391+950G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134324 | ||||||
chr10:15134354
|
G | A | 1 | a0001c0001t0006g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.391+920C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134354 | ||||||
chr10:15134442
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.391+832C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134442 | ||||||
chr10:15134454
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0219a0001c0001t0001g0266 | 3 | HG02071.hp2 NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.391+820G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134454 | ||||||
chr10:15134564
|
A | T | 3 | a0001c0002t0005g0143a0001c0002t0031g0270a0001c0002t0032g0101 | 3 | HG02615.hp1 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.391+710T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134564 | ||||||
chr10:15134572
|
C | T | 14 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+702G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134572 | ||||||
chr10:15134599
|
C | T | 3 | a0001c0004t0013g0112a0001c0004t0013g0113a0001c0004t0025g0096 | 3 | HG01975.hp2 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.391+675G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134599 | ||||||
chr10:15134791
|
A | G | 66 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(63): Show | 66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.391+483T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134791 | ||||||
chr10:15134814
|
T | C | 66 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(63): Show | 66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.391+460A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134814 | ||||||
chr10:15134947
|
C | T | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.391+327G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134947 | ||||||
chr10:15135049
|
G | A | 10 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.391+225C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135049 | ||||||
chr10:15135125
|
G | C | 7 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+149C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135125 | ||||||
chr10:15135190
|
G | GGT | 4 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(1): Show | 4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+83_391+84insAC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135190 | ||||||
chr10:15135190
|
GT | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.391+83delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135190 | ||||||
chr10:15135192
|
T | G | 41 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(38): Show | 41 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.391+82A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135192 | ||||||
chr10:15135192
|
T | TTTG | 34 | a0001c0001t0001g0064a0001c0001t0001g0171a0001c0001t0001g0200others(31): Show | 34 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.391+79_391+81dupCA others(1): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135192 | ||||||
chr10:15135200
|
T | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.391+74A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135200 | ||||||
chr10:15135238
|
T | C | 36 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.391+36A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135238 | ||||||
chr10:15135542
|
C | T | 1 | a0001c0001t0009g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.247-124G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135542 | ||||||
chr10:15135731
|
G | A | 53 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(50): Show | 53 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.247-313C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135731 | ||||||
chr10:15135775
|
T | TG | 24 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.247-358dupC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135775 | ||||||
chr10:15135779
|
T | G | 50 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(47): Show | 50 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.247-361A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135779 | ||||||
chr10:15135780
|
G | A | 13 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238others(10): Show | 13 | HG01109.hp1 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.247-362C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135780 | ||||||
chr10:15135780
|
G | T | 1 | a0001c0002t0010g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247-362C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135780 | ||||||
chr10:15135828
|
A | G | 67 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(64): Show | 67 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.247-410T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135828 | ||||||
chr10:15135908
|
CAAAG | C | 3 | a0001c0001t0001g0267a0001c0001t0004g0002a0001c0001t0004g0095 | 3 | HG02615.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.247-494_247-491del others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135908 | ||||||
chr10:15135969
|
A | AT | 3 | a0001c0002t0005g0143a0001c0002t0031g0270a0001c0002t0032g0101 | 3 | HG02615.hp1 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.247-552dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135969 | ||||||
chr10:15135997
|
T | C | 95 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(92): Show | 95 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.247-579A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135997 | ||||||
chr10:15136046
|
G | A | 11 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(8): Show | 11 | HG01975.hp2 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-628C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136046 | ||||||
chr10:15136175
|
C | T | 2 | a0001c0001t0009g0046a0001c0001t0009g0066 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.247-757G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136175 | ||||||
chr10:15136176
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247-758C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136176 | ||||||
chr10:15136177
|
C | T | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.247-759G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136177 | ||||||
chr10:15136212
|
ACT | A | 3 | a0001c0001t0009g0003a0001c0001t0009g0168a0001c0001t0009g0202 | 3 | HG00639.hp1 HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.247-796_247-795del others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136212 | ||||||
chr10:15136223
|
A | AAAGGGAA others(20): Show |
5 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-832_247-806dup others(27): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136223 | ||||||
chr10:15136232
|
G | A | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.247-814C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136232 | ||||||
chr10:15136253
|
G | A | 1 | a0001c0001t0005g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.247-835C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136253 | ||||||
chr10:15136395
|
AG | A | 5 | a0001c0002t0005g0143a0001c0002t0019g0130a0001c0002t0019g0131others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-978delC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136395 | ||||||
chr10:15136397
|
G | C | 1 | a0001c0001t0001g0226 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.247-979C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136397 | ||||||
chr10:15136398
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.247-980C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136398 | ||||||
chr10:15136400
|
G | A | 37 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0002g0047others(34): Show | 37 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.247-982C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136400 | ||||||
chr10:15136460
|
G | C | 35 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0155others(32): Show | 35 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.247-1042C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136460 | ||||||
chr10:15136677
|
C | G | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-1259G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136677 | ||||||
chr10:15136679
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.247-1261C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136679 | ||||||
chr10:15136694
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.247-1276C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136694 | ||||||
chr10:15136727
|
T | C | 49 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(46): Show | 49 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.247-1309A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136727 | ||||||
chr10:15136743
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.247-1325A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136743 | ||||||
chr10:15136827
|
CT | C | 110 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.247-1410delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136827 | ||||||
chr10:15136827
|
CTTT | C | 10 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-1412_247-1410d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136827 | ||||||
chr10:15136903
|
C | T | 32 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(29): Show | 32 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.247-1485G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136903 | ||||||
chr10:15136962
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.247-1544A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136962 | ||||||
chr10:15137082
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.247-1664T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137082 | ||||||
chr10:15137096
|
G | A | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.247-1678C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137096 | ||||||
chr10:15137191
|
G | T | 128 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(125): Show | 128 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.247-1773C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137191 | ||||||
chr10:15137378
|
A | T | 69 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0093others(66): Show | 69 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.247-1960T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137378 | ||||||
chr10:15137736
|
C | A | 32 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0093others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.247-2318G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137736 | ||||||
chr10:15137740
|
G | T | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247-2322C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137740 | ||||||
chr10:15138004
|
C | CT | 54 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0031others(51): Show | 54 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2587dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138004 | ||||||
chr10:15138004
|
C | CTT | 5 | a0001c0001t0001g0029a0001c0001t0007g0198a0001c0001t0009g0046others(2): Show | 5 | HG01884.hp2 HG02630.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-2588_247-2587d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138004 | ||||||
chr10:15138109
|
C | A | 34 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0085others(31): Show | 34 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.247-2691G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138109 | ||||||
chr10:15138257
|
C | T | 8 | a0001c0004t0013g0112a0001c0004t0013g0113a0001c0004t0025g0096others(5): Show | 8 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.247-2839G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138257 | ||||||
chr10:15138358
|
A | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0008g0092 | 3 | HG00438.hp2 HG02074.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.247-2940T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138358 | ||||||
chr10:15138452
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0252 | 2 | HG00621.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.246+2970C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138452 | ||||||
chr10:15138504
|
C | T | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.246+2918G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138504 | ||||||
chr10:15138554
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.246+2868T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138554 | ||||||
chr10:15138647
|
A | C | 1 | a0001c0001t0022g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.246+2775T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138647 | ||||||
chr10:15138709
|
A | G | 1 | a0001c0001t0041g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.246+2713T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138709 | ||||||
chr10:15138731
|
T | C | 2 | a0001c0004t0013g0112a0001c0004t0025g0096 | 2 | HG01975.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.246+2691A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138731 | ||||||
chr10:15138994
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.246+2428G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138994 | ||||||
chr10:15139130
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0069 | 3 | HG00099.hp1 HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.246+2292C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139130 | ||||||
chr10:15139250
|
C | CTCTA | 62 | a0001c0001t0001g0019a0001c0001t0001g0136a0001c0001t0001g0138others(59): Show | 62 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.246+2168_246+2171d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | ||||||
chr10:15139250
|
CTCTA | C | 61 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0001g0059others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.246+2168_246+2171d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | ||||||
chr10:15139250
|
CTCTATCT others(1): Show |
C | 7 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG00423.hp1 HG00558.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+2164_246+2171d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | ||||||
chr10:15139250
|
CTCTATCT others(5): Show |
C | 1 | a0001c0001t0001g0157 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.246+2160_246+2171d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | ||||||
chr10:15139277
|
TATCTATC others(13): Show |
T | 4 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(1): Show | 4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+2125_246+2144d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139277 | ||||||
chr10:15139293
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0028g0118 | 2 | HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.246+2129A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | ||||||
chr10:15139293
|
T | TATCC | 3 | a0001c0001t0009g0202a0001c0006t0016g0010a0001c0006t0027g0015 | 3 | HG02257.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.246+2125_246+2128d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | ||||||
chr10:15139293
|
T | TATCTATC others(1): Show |
22 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(19): Show | 22 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.246+2128_246+2129i others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | ||||||
chr10:15139293
|
T | TATCTATC others(5): Show |
1 | a0001c0001t0002g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+2128_246+2129i others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | ||||||
chr10:15139398
|
C | T | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.246+2024G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139398 | ||||||
chr10:15139510
|
G | A | 1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246+1912C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139510 | ||||||
chr10:15139570
|
T | G | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1852A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139570 | ||||||
chr10:15139606
|
G | C | 1 | a0001c0001t0011g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.246+1816C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139606 | ||||||
chr10:15139737
|
C | G | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+1685G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139737 | ||||||
chr10:15139863
|
C | CCATATA | 5 | a0001c0004t0013g0112a0001c0004t0013g0113a0001c0004t0025g0096others(2): Show | 5 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1558_246+1559i others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
C | CTA | 10 | a0001c0001t0001g0139a0001c0001t0001g0174a0001c0001t0001g0196others(7): Show | 10 | HG00423.hp2 HG00735.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.246+1557_246+1558d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
C | CTATA | 7 | a0001c0001t0001g0004a0001c0001t0001g0141a0001c0001t0001g0181others(4): Show | 7 | HG00140.hp1 HG01071.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+1555_246+1558d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
C | CTATATA | 9 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0057others(6): Show | 9 | HG00280.hp1 HG01109.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+1553_246+1558d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
C | CTATATAT others(1): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0009g0097 | 3 | HG02155.hp1 NA18906.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.246+1551_246+1558d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0242 | 2 | HG01975.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.246+1549_246+1558d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTA | C | 48 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0034others(45): Show | 48 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.246+1557_246+1558d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATA | C | 63 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.246+1555_246+1558d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATA | C | 13 | a0001c0001t0001g0136a0001c0001t0001g0144a0001c0001t0001g0151others(10): Show | 13 | HG01099.hp2 HG01243.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.246+1553_246+1558d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(1): Show |
C | 6 | a0001c0001t0001g0253a0001c0001t0012g0077a0001c0001t0024g0074others(3): Show | 6 | HG00140.hp2 HG01109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+1551_246+1558d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(3): Show |
C | 2 | a0001c0001t0001g0194a0001c0002t0010g0126 | 2 | HG01074.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.246+1549_246+1558d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(5): Show |
C | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.246+1547_246+1558d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(7): Show |
C | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246+1545_246+1558d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(11): Show |
C | 4 | a0001c0001t0003g0052a0001c0001t0003g0070a0001c0001t0021g0263others(1): Show | 4 | HG00642.hp2 HG01081.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1541_246+1558d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(13): Show |
C | 25 | a0001c0001t0001g0064a0001c0001t0001g0091a0001c0001t0001g0093others(22): Show | 25 | HG00438.hp2 HG00735.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.246+1539_246+1558d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(15): Show |
C | 50 | a0001c0001t0001g0035a0001c0001t0001g0140a0001c0001t0001g0155others(47): Show | 50 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.246+1537_246+1558d others(24): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(17): Show |
C | 2 | a0001c0001t0001g0075a0001c0002t0010g0090 | 2 | HG00738.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.246+1535_246+1558d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139863
|
CTATATAT others(21): Show |
C | 4 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(1): Show | 4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1531_246+1558d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | ||||||
chr10:15139864
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0007g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.246+1545_246+1557d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139864 | ||||||
chr10:15139866
|
T | C | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.246+1556A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139866 | ||||||
chr10:15139868
|
T | C | 1 | a0001c0005t0003g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246+1554A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139868 | ||||||
chr10:15139870
|
T | C | 1 | a0001c0005t0003g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.246+1552A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139870 | ||||||
chr10:15139872
|
T | C | 3 | a0001c0002t0015g0102a0001c0002t0015g0123a0001c0002t0015g0124 | 3 | HG01109.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.246+1550A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139872 | ||||||
chr10:15139874
|
T | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.246+1548A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139874 | ||||||
chr10:15139878
|
T | C | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246+1544A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139878 | ||||||
chr10:15139882
|
T | C | 3 | a0001c0001t0003g0052a0001c0001t0003g0070a0001c0001t0042g0225 | 3 | HG00642.hp2 HG01081.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.246+1540A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139882 | ||||||
chr10:15139883
|
A | T | 1 | a0001c0004t0013g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.246+1539T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139883 | ||||||
chr10:15139884
|
T | C | 24 | a0001c0001t0001g0064a0001c0001t0001g0093a0001c0001t0001g0094others(21): Show | 24 | HG00438.hp2 HG00735.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.246+1538A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139884 | ||||||
chr10:15139886
|
T | C | 47 | a0001c0001t0001g0035a0001c0001t0001g0155a0001c0001t0001g0267others(44): Show | 47 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.246+1536A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139886 | ||||||
chr10:15139888
|
T | C | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+1534A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139888 | ||||||
chr10:15140014
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.246+1408C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140014 | ||||||
chr10:15140103
|
C | T | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.246+1319G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140103 | ||||||
chr10:15140130
|
T | C | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.246+1292A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140130 | ||||||
chr10:15140183
|
C | T | 3 | a0001c0001t0006g0108a0001c0001t0006g0110a0001c0001t0006g0115 | 3 | HG02280.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.246+1239G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140183 | ||||||
chr10:15140277
|
C | T | 2 | a0001c0001t0009g0003a0001c0001t0009g0168 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.246+1145G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140277 | ||||||
chr10:15140299
|
T | A | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+1123A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140299 | ||||||
chr10:15140525
|
T | C | 4 | a0001c0004t0013g0112a0001c0004t0013g0113a0001c0004t0025g0096others(1): Show | 4 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+897A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140525 | ||||||
chr10:15140573
|
A | G | 1 | a0001c0001t0004g0269 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.246+849T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140573 | ||||||
chr10:15140591
|
C | T | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.246+831G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140591 | ||||||
chr10:15140619
|
T | G | 81 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0064others(78): Show | 81 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.246+803A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140619 | ||||||
chr10:15140632
|
C | A | 15 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(12): Show | 15 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+790G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140632 | ||||||
chr10:15140894
|
A | G | 4 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(1): Show | 4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+528T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140894 | ||||||
chr10:15141160
|
G | A | 32 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(29): Show | 32 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.246+262C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15141160 | ||||||
chr10:15141354
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246+68C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15141354 | ||||||
chr10:15141364
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.246+58C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15141364 | ||||||
chr10:15141748
|
GC | G | 7 | a0001c0001t0004g0103a0001c0001t0004g0104a0001c0001t0004g0105others(4): Show | 7 | HG01243.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-192delG | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141748 | ||||||
chr10:15141771
|
G | A | 2 | a0001c0005t0003g0125a0001c0005t0003g0129 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.111-214C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141771 | ||||||
chr10:15141859
|
T | A | 71 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0064others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.111-302A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141859 | ||||||
chr10:15141927
|
T | C | 3 | a0001c0005t0003g0125a0001c0005t0003g0129a0001c0005t0009g0128 | 3 | HG03098.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.111-370A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141927 | ||||||
chr10:15141969
|
T | G | 4 | a0001c0002t0014g0073a0001c0002t0014g0087a0001c0002t0014g0088others(1): Show | 4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-412A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141969 | ||||||
chr10:15141998
|
A | G | 5 | a0001c0001t0001g0019a0001c0002t0002g0017a0001c0002t0002g0142others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-441T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141998 | ||||||
chr10:15142051
|
G | A | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-494C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142051 | ||||||
chr10:15142273
|
C | T | 1 | a0001c0001t0006g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.111-716G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142273 | ||||||
chr10:15142401
|
GA | G | 32 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(29): Show | 32 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.111-845delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142401 | ||||||
chr10:15142421
|
G | C | 9 | a0001c0001t0009g0003a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-864C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142421 | ||||||
chr10:15142506
|
G | A | 71 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0064others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.111-949C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142506 | ||||||
chr10:15142519
|
G | A | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-962C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142519 | ||||||
chr10:15142528
|
C | T | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-971G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142528 | ||||||
chr10:15142585
|
T | C | 2 | a0001c0002t0018g0268a0001c0002t0018g0271 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.111-1028A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142585 | ||||||
chr10:15142625
|
T | C | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.111-1068A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142625 | ||||||
chr10:15142744
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.111-1187G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142744 | ||||||
chr10:15142881
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111-1324T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142881 | ||||||
chr10:15143033
|
G | T | 4 | a0001c0002t0002g0017a0001c0002t0002g0142a0001c0002t0002g0238others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-1476C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143033 | ||||||
chr10:15143110
|
T | C | 5 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-1553A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143110 | ||||||
chr10:15143213
|
A | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0031others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.111-1656T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143213 | ||||||
chr10:15143295
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.111-1738G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143295 | ||||||
chr10:15143331
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.111-1774G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143331 | ||||||
chr10:15143502
|
G | C | 9 | a0001c0001t0009g0097a0001c0001t0011g0007a0001c0001t0011g0008others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-1945C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143502 | ||||||
chr10:15143504
|
C | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0026others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.111-1947G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143504 | ||||||
chr10:15143542
|
T | C | 25 | a0001c0001t0001g0091a0001c0001t0001g0231a0001c0001t0006g0081others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.111-1985A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143542 | ||||||
chr10:15143581
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.111-2024C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143581 | ||||||
chr10:15143582
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.111-2025G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143582 | ||||||
chr10:15143588
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.111-2031C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143588 | ||||||
chr10:15143602
|
A | C | 1 | a0001c0001t0036g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.111-2045T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143602 | ||||||
chr10:15143636
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.111-2079G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143636 | ||||||
chr10:15143747
|
G | A | 22 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0245others(19): Show | 22 | HG01109.hp1 HG01175.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.111-2190C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143747 | ||||||
chr10:15143842
|
G | T | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-2285C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143842 | ||||||
chr10:15143978
|
A | G | 5 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(2): Show | 5 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-2421T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143978 | ||||||
chr10:15144041
|
CA | C | 16 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-2485delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144041 | ||||||
chr10:15144209
|
T | C | 1 | a0001c0001t0008g0189 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.111-2652A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144209 | ||||||
chr10:15144263
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.111-2706G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144263 | ||||||
chr10:15144372
|
C | T | 2 | a0001c0001t0033g0107a0001c0001t0045g0050 | 2 | HG02109.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.111-2815G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144372 | ||||||
chr10:15144405
|
C | T | 8 | a0001c0001t0009g0046a0001c0001t0009g0066a0001c0001t0022g0080others(5): Show | 8 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-2848G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144405 | ||||||
chr10:15144457
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.111-2900A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144457 | ||||||
chr10:15144478
|
T | C | 8 | a0001c0001t0001g0019a0001c0004t0013g0112a0001c0004t0025g0096others(5): Show | 8 | HG01975.hp2 HG02896.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-2921A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144478 | ||||||
chr10:15144526
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.111-2969A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144526 | ||||||
chr10:15144527
|
C | G | 6 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(3): Show | 6 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-2970G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144527 | ||||||
chr10:15144594
|
G | A | 17 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(14): Show | 17 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.111-3037C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144594 | ||||||
chr10:15144598
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(3): Show | 6 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-3041C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144598 | ||||||
chr10:15144678
|
C | T | 104 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(101): Show | 104 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.111-3121G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144678 | ||||||
chr10:15144679
|
C | G | 104 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(101): Show | 104 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.111-3122G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144679 | ||||||
chr10:15144706
|
G | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(106): Show | 109 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.111-3149C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144706 | ||||||
chr10:15144718
|
G | A | 5 | a0001c0001t0012g0077a0001c0001t0012g0078a0001c0001t0012g0079others(2): Show | 5 | HG00140.hp2 HG01261.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-3161C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144718 | ||||||
chr10:15144725
|
C | T | 8 | a0001c0001t0006g0048a0001c0001t0009g0046a0001c0001t0009g0066others(5): Show | 8 | HG01192.hp2 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-3168G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144725 | ||||||
chr10:15144821
|
G | T | 112 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(109): Show | 112 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.111-3264C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144821 | ||||||
chr10:15145337
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.111-3780G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145337 | ||||||
chr10:15145382
|
T | C | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.111-3825A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145382 | ||||||
chr10:15145582
|
G | A | 1 | a0001c0001t0009g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111-4025C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145582 | ||||||
chr10:15145722
|
T | G | 9 | a0001c0001t0006g0048a0001c0001t0009g0046a0001c0001t0009g0066others(6): Show | 9 | HG01192.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-4165A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145722 | ||||||
chr10:15145757
|
A | T | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.111-4200T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145757 | ||||||
chr10:15145799
|
C | T | 16 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-4242G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145799 | ||||||
chr10:15145834
|
G | T | 16 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-4277C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145834 | ||||||
chr10:15145839
|
C | T | 33 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(30): Show | 33 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.111-4282G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145839 | ||||||
chr10:15145840
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.111-4283C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145840 | ||||||
chr10:15145907
|
G | A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111-4350C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145907 | ||||||
chr10:15145929
|
C | T | 2 | a0001c0001t0003g0152a0001c0001t0003g0233 | 2 | HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-4372G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145929 | ||||||
chr10:15145951
|
G | T | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(104): Show | 107 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.111-4394C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145951 | ||||||
chr10:15146596
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.111-5039T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146596 | ||||||
chr10:15146612
|
G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-5055C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146612 | ||||||
chr10:15146627
|
G | A | 5 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(2): Show | 5 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-5070C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146627 | ||||||
chr10:15146738
|
C | T | 6 | a0001c0002t0010g0126a0001c0002t0015g0102a0001c0002t0015g0123others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-5181G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146738 | ||||||
chr10:15146756
|
G | C | 17 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(14): Show | 17 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.111-5199C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146756 | ||||||
chr10:15146785
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.111-5228T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146785 | ||||||
chr10:15146830
|
C | T | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111-5273G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146830 | ||||||
chr10:15147069
|
G | A | 1 | a0001c0001t0008g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.111-5512C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147069 | ||||||
chr10:15147095
|
C | CA | 36 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0059others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.111-5539dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-5550_111-5539d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.111-5551_111-5539d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CA | C | 30 | a0001c0001t0001g0032a0001c0001t0001g0136a0001c0001t0001g0151others(27): Show | 30 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.111-5539delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111-5548_111-5539d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.111-5549_111-5539d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0002t0010g0011a0001c0002t0010g0012a0002c0008t0010g0013 | 3 | HG02647.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.111-5550_111-5539d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0002g0063a0001c0001t0003g0061a0001c0001t0003g0072others(2): Show | 5 | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-5551_111-5539d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(7): Show |
C | 12 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(9): Show | 12 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-5552_111-5539d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0035g0114a0001c0004t0013g0113a0001c0004t0025g0096others(4): Show | 7 | HG01975.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-5554_111-5539d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(10): Show |
C | 15 | a0001c0001t0001g0019a0001c0001t0001g0091a0001c0001t0006g0108others(12): Show | 15 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.111-5555_111-5539d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(11): Show |
C | 29 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(26): Show | 29 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.111-5556_111-5539d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0002g0027a0001c0001t0004g0273a0001c0004t0048g0016 | 3 | HG02965.hp1 NA18984.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.111-5557_111-5539d others(21): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(13): Show |
C | 20 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(17): Show | 20 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-5558_111-5539d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(16): Show |
C | 9 | a0001c0001t0004g0269a0001c0002t0010g0126a0001c0002t0015g0102others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-5561_111-5539d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147095
|
CAAAAAAA others(20): Show |
C | 1 | a0001c0003t0008g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.111-5565_111-5539d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | ||||||
chr10:15147411
|
A | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0151a0001c0001t0001g0174others(3): Show | 6 | HG01109.hp2 HG01258.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-5854T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147411 | ||||||
chr10:15147436
|
G | A | 9 | a0001c0001t0004g0269a0001c0002t0010g0126a0001c0002t0015g0102others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-5879C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147436 | ||||||
chr10:15147519
|
T | C | 1 | a0001c0004t0025g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.111-5962A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147519 | ||||||
chr10:15147625
|
C | T | 1 | a0001c0001t0013g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.111-6068G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147625 | ||||||
chr10:15147635
|
G | GA | 13 | a0001c0001t0001g0019a0001c0001t0002g0024a0001c0001t0004g0095others(10): Show | 13 | HG02258.hp2 HG02647.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-6079dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147635 | ||||||
chr10:15147697
|
T | G | 28 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(25): Show | 28 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.111-6140A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147697 | ||||||
chr10:15147850
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.111-6293G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147850 | ||||||
chr10:15148103
|
C | T | 1 | a0001c0001t0009g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111-6546G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148103 | ||||||
chr10:15148320
|
A | G | 7 | a0001c0001t0001g0134a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-6763T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148320 | ||||||
chr10:15148580
|
G | A | 24 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(21): Show | 24 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.111-7023C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148580 | ||||||
chr10:15148600
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.111-7043T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148600 | ||||||
chr10:15148604
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111-7047C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148604 | ||||||
chr10:15148612
|
C | T | 16 | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0002g0047others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-7055G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148612 | ||||||
chr10:15148683
|
C | T | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7126G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148683 | ||||||
chr10:15148808
|
A | AC | 18 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(15): Show | 18 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-7252_111-7251i others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148808 | ||||||
chr10:15148877
|
A | C | 18 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(15): Show | 18 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-7320T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148877 | ||||||
chr10:15148888
|
A | T | 62 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(59): Show | 62 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.111-7331T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148888 | ||||||
chr10:15148931
|
C | A | 1 | a0001c0001t0005g0237 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.111-7374G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148931 | ||||||
chr10:15149133
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.111-7576C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149133 | ||||||
chr10:15149148
|
C | T | 116 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(113): Show | 116 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.111-7591G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149148 | ||||||
chr10:15149149
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.111-7592C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149149 | ||||||
chr10:15149192
|
C | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-7635G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149192 | ||||||
chr10:15149198
|
TCAC | T | 7 | a0001c0001t0001g0133a0001c0001t0001g0148a0001c0001t0008g0147others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-7644_111-7642d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149198 | ||||||
chr10:15149314
|
CCAT | C | 4 | a0001c0001t0013g0111a0001c0004t0013g0112a0001c0004t0013g0113others(1): Show | 4 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7760_111-7758d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149314 | ||||||
chr10:15149442
|
C | CCACCATC others(539): Show |
6 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(3): Show | 6 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(548): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
3 | a0001c0001t0004g0269a0001c0002t0018g0268a0001c0002t0018g0271 | 3 | HG01243.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(539): Show |
4 | a0001c0002t0010g0126a0001c0002t0015g0102a0001c0002t0015g0123others(1): Show | 4 | HG01109.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(548): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(533): Show |
4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(542): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(521): Show |
1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(530): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(526): Show |
2 | a0001c0001t0009g0003a0001c0001t0009g0168 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(535): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(512): Show |
1 | a0001c0001t0007g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(521): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(518): Show |
1 | a0001c0001t0001g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0138 | 2 | HG00140.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
1 | a0001c0001t0001g0215 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
1 | a0001c0001t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(530): Show |
149 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0032others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
1 | a0001c0001t0007g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(527): Show |
3 | a0001c0001t0022g0080a0001c0001t0041g0044a0001c0001t0049g0206 | 3 | HG01192.hp2 HG03139.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(518): Show |
5 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(530): Show |
2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(518): Show |
4 | a0001c0001t0009g0097a0001c0001t0024g0074a0001c0001t0052g0067others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(530): Show |
63 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(530): Show |
1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(512): Show |
15 | a0001c0001t0001g0064a0001c0001t0002g0047a0001c0001t0002g0063others(12): Show | 15 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(521): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149442
|
C | CCACCATC others(518): Show |
1 | a0001c0001t0006g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | ||||||
chr10:15149446
|
C | CATCACAT others(530): Show |
1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-7890_111-7889i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149446 | ||||||
chr10:15149466
|
T | C | 3 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009 | 3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.111-7909A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149466 | ||||||
chr10:15149562
|
ACATCATC others(5): Show |
A | 17 | a0001c0001t0001g0019a0001c0001t0001g0134a0001c0001t0002g0063others(14): Show | 17 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.111-8017_111-8006d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149562 | ||||||
chr10:15149604
|
T | A | 98 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(95): Show | 98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.111-8047A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149604 | ||||||
chr10:15149817
|
CAG | C | 13 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(10): Show | 13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-8262_111-8261d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149817 | ||||||
chr10:15149820
|
G | C | 13 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(10): Show | 13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-8263C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149820 | ||||||
chr10:15149822
|
C | T | 13 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(10): Show | 13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-8265G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149822 | ||||||
chr10:15149958
|
T | G | 1 | a0001c0001t0021g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.111-8401A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149958 | ||||||
chr10:15150229
|
C | T | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.111-8672G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150229 | ||||||
chr10:15150538
|
G | A | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-8981C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150538 | ||||||
chr10:15150609
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0250 | 2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.111-9052A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150609 | ||||||
chr10:15150765
|
C | T | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111-9208G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150765 | ||||||
chr10:15150786
|
G | A | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111-9229C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150786 | ||||||
chr10:15150828
|
A | C | 13 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(10): Show | 13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-9271T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150828 | ||||||
chr10:15150852
|
A | G | 12 | a0001c0001t0009g0097a0001c0001t0011g0007a0001c0001t0011g0008others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.111-9295T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150852 | ||||||
chr10:15150884
|
C | A | 1 | a0001c0001t0005g0236 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111-9327G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150884 | ||||||
chr10:15151059
|
C | CTTTTTT | 11 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(8): Show | 11 | HG00140.hp2 HG01109.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.111-9508_111-9503d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151059 | ||||||
chr10:15151059
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-9503_111-9502i others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151059 | ||||||
chr10:15151061
|
T | C | 2 | a0001c0002t0002g0017a0001c0002t0012g0018 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.111-9504A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151061 | ||||||
chr10:15151075
|
G | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-9518C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151075 | ||||||
chr10:15151127
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.111-9570G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151127 | ||||||
chr10:15151128
|
G | A | 4 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0002t0010g0090others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-9571C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151128 | ||||||
chr10:15151243
|
G | A | 1 | a0001c0001t0051g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.111-9686C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151243 | ||||||
chr10:15151245
|
C | T | 1 | a0001c0001t0022g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.111-9688G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151245 | ||||||
chr10:15151290
|
C | T | 26 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(23): Show | 26 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.111-9733G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151290 | ||||||
chr10:15151425
|
G | A | 24 | a0001c0001t0001g0064a0001c0001t0002g0047a0001c0001t0002g0063others(21): Show | 24 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.111-9868C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151425 | ||||||
chr10:15151471
|
C | T | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111-9914G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151471 | ||||||
chr10:15151479
|
C | T | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111-9922G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151479 | ||||||
chr10:15151490
|
A | C | 3 | a0001c0001t0006g0048a0001c0001t0009g0046a0001c0001t0009g0066 | 3 | HG01884.hp2 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.111-9933T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151490 | ||||||
chr10:15151514
|
T | C | 5 | a0001c0001t0004g0103a0001c0001t0004g0104a0001c0001t0004g0105others(2): Show | 5 | HG02723.hp1 HG02922.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-9957A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151514 | ||||||
chr10:15151842
|
T | C | 4 | a0001c0001t0001g0134a0001c0001t0012g0077a0001c0001t0012g0078others(1): Show | 4 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-10285A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151842 | ||||||
chr10:15151898
|
C | T | 26 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(23): Show | 26 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.111-10341G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151898 | ||||||
chr10:15152032
|
A | C | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-10475T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152032 | ||||||
chr10:15152049
|
G | A | 14 | a0001c0001t0001g0134a0001c0001t0004g0269a0001c0001t0012g0077others(11): Show | 14 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-10492C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152049 | ||||||
chr10:15152058
|
A | C | 10 | a0001c0001t0001g0019a0001c0001t0013g0111a0001c0004t0013g0112others(7): Show | 10 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-10501T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152058 | ||||||
chr10:15152268
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.111-10711T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152268 | ||||||
chr10:15152295
|
C | A | 33 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(30): Show | 33 | HG00438.hp2 HG00642.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.111-10738G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152295 | ||||||
chr10:15152362
|
A | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG00280.hp2 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-10805T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152362 | ||||||
chr10:15152577
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.111-11020C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152577 | ||||||
chr10:15152845
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.111-11288C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152845 | ||||||
chr10:15153004
|
T | C | 10 | a0001c0001t0006g0108a0001c0001t0006g0109a0001c0001t0006g0110others(7): Show | 10 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-11447A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153004 | ||||||
chr10:15153009
|
C | T | 1 | a0001c0001t0040g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111-11452G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153009 | ||||||
chr10:15153028
|
T | C | 3 | a0001c0002t0010g0011a0001c0002t0010g0012a0002c0008t0010g0013 | 3 | HG02647.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.111-11471A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153028 | ||||||
chr10:15153089
|
T | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0134others(9): Show | 12 | HG00140.hp2 HG01243.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-11532A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153089 | ||||||
chr10:15153104
|
C | T | 1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.111-11547G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153104 | ||||||
chr10:15153121
|
C | A | 2 | a0001c0001t0009g0003a0001c0001t0009g0168 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.111-11564G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153121 | ||||||
chr10:15153333
|
G | A | 3 | a0001c0001t0009g0097a0001c0001t0052g0067a0001c0005t0003g0125 | 3 | HG02451.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.111-11776C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153333 | ||||||
chr10:15153373
|
T | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0076a0001c0001t0001g0134others(8): Show | 11 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.111-11816A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153373 | ||||||
chr10:15153406
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.111-11849A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153406 | ||||||
chr10:15153432
|
C | T | 2 | a0001c0002t0002g0142a0001c0002t0002g0238 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.111-11875G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153432 | ||||||
chr10:15153657
|
T | A | 2 | a0001c0001t0024g0074a0001c0002t0014g0073 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.111-12100A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153657 | ||||||
chr10:15153658
|
A | T | 18 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0091others(15): Show | 18 | HG00597.hp1 HG00621.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-12101T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153658 | ||||||
chr10:15153663
|
T | A | 1 | a0001c0001t0049g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.111-12106A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153663 | ||||||
chr10:15153670
|
A | T | 1 | a0001c0001t0040g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111-12113T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153670 | ||||||
chr10:15153806
|
C | T | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111-12249G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153806 | ||||||
chr10:15153810
|
C | T | 1 | a0001c0001t0041g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111-12253G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153810 | ||||||
chr10:15153816
|
A | AT | 6 | a0001c0001t0001g0155a0001c0001t0007g0156a0001c0001t0011g0007others(3): Show | 6 | HG01123.hp2 HG01167.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-12260dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153816 | ||||||
chr10:15153843
|
C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0134a0001c0001t0012g0077others(6): Show | 9 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-12286G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153843 | ||||||
chr10:15153864
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.111-12307T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153864 | ||||||
chr10:15153899
|
C | T | 1 | a0001c0001t0003g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.111-12342G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153899 | ||||||
chr10:15153900
|
G | A | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-12343C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153900 | ||||||
chr10:15153910
|
C | A | 5 | a0001c0001t0001g0091a0001c0002t0005g0276a0001c0002t0010g0126others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-12353G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153910 | ||||||
chr10:15154070
|
T | C | 1 | a0001c0002t0032g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.111-12513A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154070 | ||||||
chr10:15154232
|
G | C | 31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(28): Show | 31 | HG00438.hp1 HG00609.hp2 HG01975.hp2 others(28): Show |
intron_variant | MODIFIER | c.111-12675C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154232 | ||||||
chr10:15154346
|
G | T | 25 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(22): Show | 25 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.111-12789C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154346 | ||||||
chr10:15154368
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.111-12811G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154368 | ||||||
chr10:15154373
|
G | A | 5 | a0001c0002t0010g0012a0001c0006t0016g0010a0001c0006t0016g0014others(2): Show | 5 | HG02647.hp1 HG02970.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-12816C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154373 | ||||||
chr10:15154384
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.111-12827C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154384 | ||||||
chr10:15154475
|
G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-12918C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154475 | ||||||
chr10:15154587
|
A | G | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-13030T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154587 | ||||||
chr10:15154631
|
T | C | 27 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(24): Show | 27 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.111-13074A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154631 | ||||||
chr10:15154665
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0034g0098a0001c0002t0002g0017others(1): Show | 4 | HG02809.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-13108T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154665 | ||||||
chr10:15154992
|
G | T | 2 | a0001c0001t0021g0051a0001c0001t0045g0050 | 2 | NA18955.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.111-13435C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154992 | ||||||
chr10:15155077
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.110+13426T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155077 | ||||||
chr10:15155462
|
G | A | 1 | a0001c0001t0052g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110+13041C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155462 | ||||||
chr10:15155472
|
G | A | 9 | a0001c0001t0001g0076a0001c0001t0001g0134a0001c0001t0012g0077others(6): Show | 9 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.110+13031C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155472 | ||||||
chr10:15155529
|
G | A | 1 | a0001c0001t0050g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110+12974C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155529 | ||||||
chr10:15155535
|
G | GT | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0049others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+12967dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | ||||||
chr10:15155535
|
GT | G | 137 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0035others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.110+12967delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | ||||||
chr10:15155535
|
GTT | G | 66 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(63): Show | 66 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.110+12966_110+1296 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | ||||||
chr10:15155535
|
GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0034 | 3 | NA18940.hp2 NA19012.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.110+12956_110+1296 others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | ||||||
chr10:15155535
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+12955_110+1296 others(17): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | ||||||
chr10:15155535
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0002t0002g0017a0001c0002t0012g0018 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.110+12954_110+1296 others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | ||||||
chr10:15155634
|
T | C | 61 | a0001c0001t0001g0019a0001c0001t0001g0091a0001c0001t0001g0093others(58): Show | 61 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.110+12869A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155634 | ||||||
chr10:15155635
|
G | A | 1 | a0001c0001t0035g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.110+12868C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155635 | ||||||
chr10:15155668
|
C | T | 43 | a0001c0001t0001g0019a0001c0001t0001g0091a0001c0001t0001g0093others(40): Show | 43 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+12835G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155668 | ||||||
chr10:15155677
|
C | T | 17 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0064others(14): Show | 17 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.110+12826G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155677 | ||||||
chr10:15155715
|
ATCT | A | 3 | a0001c0006t0016g0010a0001c0006t0016g0014a0001c0006t0027g0015 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.110+12785_110+1278 others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155715 | ||||||
chr10:15155740
|
C | T | 2 | a0001c0002t0002g0017a0001c0002t0012g0018 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.110+12763G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155740 | ||||||
chr10:15155777
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+12726T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155777 | ||||||
chr10:15155819
|
G | A | 1 | a0001c0001t0009g0168 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.110+12684C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155819 | ||||||
chr10:15156061
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.110+12442C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156061 | ||||||
chr10:15156124
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.110+12379C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156124 | ||||||
chr10:15156250
|
G | T | 10 | a0001c0001t0001g0144a0001c0001t0001g0171a0001c0001t0001g0172others(7): Show | 10 | HG01934.hp1 NA18940.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+12253C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156250 | ||||||
chr10:15156414
|
A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.110+12089T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156414 | ||||||
chr10:15156442
|
G | A | 6 | a0001c0001t0001g0091a0001c0002t0005g0276a0001c0002t0010g0126others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+12061C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156442 | ||||||
chr10:15156470
|
G | A | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+12033C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156470 | ||||||
chr10:15156577
|
G | C | 4 | a0001c0001t0004g0269a0001c0002t0018g0268a0001c0002t0018g0271others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+11926C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156577 | ||||||
chr10:15156585
|
T | C | 29 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0064others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+11918A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156585 | ||||||
chr10:15156625
|
G | A | 6 | a0001c0001t0001g0091a0001c0002t0005g0276a0001c0002t0010g0126others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+11878C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156625 | ||||||
chr10:15156626
|
C | T | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.110+11877G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156626 | ||||||
chr10:15156636
|
C | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+11867G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156636 | ||||||
chr10:15156783
|
C | A | 3 | a0001c0001t0005g0207a0001c0001t0005g0236a0001c0001t0005g0237 | 3 | HG02055.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.110+11720G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156783 | ||||||
chr10:15156844
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0043 | 2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.110+11659G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156844 | ||||||
chr10:15156901
|
A | C | 4 | a0001c0001t0004g0269a0001c0002t0018g0268a0001c0002t0018g0271others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+11602T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156901 | ||||||
chr10:15157082
|
T | C | 10 | a0001c0001t0009g0097a0001c0001t0011g0007a0001c0001t0011g0008others(7): Show | 10 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+11421A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157082 | ||||||
chr10:15157164
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.110+11339G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157164 | ||||||
chr10:15157223
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.110+11280G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157223 | ||||||
chr10:15157348
|
C | A | 18 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0064others(15): Show | 18 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.110+11155G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157348 | ||||||
chr10:15157433
|
C | T | 2 | a0001c0002t0010g0090a0001c0005t0009g0128 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+11070G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157433 | ||||||
chr10:15157569
|
A | G | 5 | a0001c0001t0004g0269a0001c0001t0034g0098a0001c0002t0018g0268others(2): Show | 5 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+10934T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157569 | ||||||
chr10:15157686
|
A | G | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+10817T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157686 | ||||||
chr10:15157718
|
T | A | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0200others(4): Show | 7 | HG01943.hp1 HG01952.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+10785A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157718 | ||||||
chr10:15157739
|
T | C | 1 | a0001c0001t0009g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.110+10764A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157739 | ||||||
chr10:15157754
|
T | C | 26 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054others(23): Show | 26 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+10749A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157754 | ||||||
chr10:15157778
|
T | C | 2 | a0001c0002t0002g0142a0001c0002t0002g0238 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.110+10725A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157778 | ||||||
chr10:15157823
|
C | G | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.110+10680G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157823 | ||||||
chr10:15157827
|
T | C | 5 | a0001c0001t0004g0269a0001c0001t0034g0098a0001c0002t0018g0268others(2): Show | 5 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+10676A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157827 | ||||||
chr10:15158133
|
T | C | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+10370A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158133 | ||||||
chr10:15158152
|
C | T | 1 | a0001c0001t0009g0168 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.110+10351G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158152 | ||||||
chr10:15158173
|
G | A | 10 | a0001c0001t0005g0005a0001c0001t0005g0203a0001c0001t0005g0204others(7): Show | 10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+10330C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158173 | ||||||
chr10:15158315
|
CA | C | 40 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0064others(37): Show | 40 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.110+10187delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158315 | ||||||
chr10:15158438
|
C | G | 22 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0064others(19): Show | 22 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.110+10065G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158438 | ||||||
chr10:15158561
|
A | G | 29 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+9942T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158561 | ||||||
chr10:15158608
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.110+9895A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158608 | ||||||
chr10:15158783
|
C | T | 29 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+9720G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158783 | ||||||
chr10:15158885
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | NA18999.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.110+9618G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158885 | ||||||
chr10:15159396
|
A | ATATT | 14 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0135others(11): Show | 14 | HG00597.hp2 HG00673.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+9103_110+9106d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
A | ATATTTAT others(1): Show |
21 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0064others(18): Show | 21 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.110+9099_110+9106d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
A | ATATTTAT others(5): Show |
10 | a0001c0001t0001g0040a0001c0001t0002g0041a0001c0001t0002g0047others(7): Show | 10 | HG00735.hp1 HG01081.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+9095_110+9106d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
A | ATATTTAT others(9): Show |
7 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0032others(4): Show | 7 | HG02258.hp2 HG03098.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+9091_110+9106d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
A | ATATTTAT others(13): Show |
16 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0031others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.110+9087_110+9106d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
A | ATATTTAT others(17): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0247a0001c0001t0002g0036 | 3 | HG00558.hp1 HG02155.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.110+9083_110+9106d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
ATATTTAT others(1): Show |
A | 17 | a0001c0001t0001g0076a0001c0001t0001g0134a0001c0001t0006g0081others(14): Show | 17 | HG00140.hp2 HG01192.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.110+9099_110+9106d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159396
|
ATATTTAT others(5): Show |
A | 33 | a0001c0001t0001g0019a0001c0001t0001g0093a0001c0001t0001g0094others(30): Show | 33 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+9095_110+9106d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | ||||||
chr10:15159429
|
G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+9074C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159429 | ||||||
chr10:15159553
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110+8950C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159553 | ||||||
chr10:15159639
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.110+8864C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159639 | ||||||
chr10:15159852
|
G | A | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+8651C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159852 | ||||||
chr10:15159875
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.110+8628G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159875 | ||||||
chr10:15159887
|
T | G | 31 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(28): Show | 31 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.110+8616A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159887 | ||||||
chr10:15159925
|
G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+8578C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159925 | ||||||
chr10:15159994
|
C | T | 26 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+8509G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159994 | ||||||
chr10:15160215
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.110+8288G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160215 | ||||||
chr10:15160254
|
T | C | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8249A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160254 | ||||||
chr10:15160338
|
A | T | 29 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+8165T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160338 | ||||||
chr10:15160448
|
A | ACATG | 4 | a0001c0001t0004g0269a0001c0002t0018g0268a0001c0002t0018g0271others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+8051_110+8054d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160448 | ||||||
chr10:15160507
|
G | C | 2 | a0001c0002t0010g0090a0001c0005t0009g0128 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+7996C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160507 | ||||||
chr10:15160534
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0134others(3): Show | 6 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7969C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160534 | ||||||
chr10:15160554
|
T | G | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+7949A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160554 | ||||||
chr10:15160573
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.110+7930C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160573 | ||||||
chr10:15160582
|
C | T | 28 | a0001c0001t0001g0019a0001c0001t0001g0093a0001c0001t0001g0094others(25): Show | 28 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+7921G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160582 | ||||||
chr10:15160583
|
G | A | 10 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0134others(7): Show | 10 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+7920C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160583 | ||||||
chr10:15160727
|
T | A | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.110+7776A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160727 | ||||||
chr10:15160817
|
G | C | 1 | a0001c0001t0050g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110+7686C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160817 | ||||||
chr10:15160874
|
C | T | 2 | a0001c0001t0034g0098a0001c0002t0014g0073 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.110+7629G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160874 | ||||||
chr10:15161061
|
C | G | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.110+7442G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161061 | ||||||
chr10:15161081
|
C | CA | 78 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(75): Show | 78 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.110+7421dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | ||||||
chr10:15161081
|
C | CAA | 25 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(22): Show | 25 | HG00140.hp2 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.110+7420_110+7421d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | ||||||
chr10:15161081
|
CA | C | 33 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0093others(30): Show | 33 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.110+7421delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | ||||||
chr10:15161081
|
CAA | C | 21 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.110+7420_110+7421d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | ||||||
chr10:15161102
|
A | C | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7401T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161102 | ||||||
chr10:15161276
|
C | T | 85 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.110+7227G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161276 | ||||||
chr10:15161311
|
A | C | 28 | a0001c0001t0001g0019a0001c0001t0001g0093a0001c0001t0001g0094others(25): Show | 28 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+7192T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161311 | ||||||
chr10:15161391
|
G | A | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7112C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161391 | ||||||
chr10:15161548
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.110+6955A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161548 | ||||||
chr10:15161602
|
C | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+6901G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161602 | ||||||
chr10:15161683
|
C | T | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.110+6820G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161683 | ||||||
chr10:15161948
|
A | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0002g0158others(4): Show | 7 | HG01099.hp1 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+6555T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161948 | ||||||
chr10:15162251
|
C | CA | 13 | a0001c0001t0001g0069a0001c0001t0001g0240a0001c0001t0001g0241others(10): Show | 13 | HG00673.hp1 HG00735.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.110+6251dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162251 | ||||||
chr10:15162251
|
CA | C | 18 | a0001c0001t0001g0033a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 18 | HG00140.hp2 HG00738.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.110+6251delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162251 | ||||||
chr10:15162251
|
CAA | C | 26 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+6250_110+6251d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162251 | ||||||
chr10:15162370
|
G | T | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+6133C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162370 | ||||||
chr10:15162437
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.110+6066C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162437 | ||||||
chr10:15162464
|
A | T | 29 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+6039T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162464 | ||||||
chr10:15162567
|
C | A | 1 | a0001c0001t0006g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.110+5936G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162567 | ||||||
chr10:15162569
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.110+5934G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162569 | ||||||
chr10:15162653
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.110+5850T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162653 | ||||||
chr10:15162747
|
G | GAT | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0134others(10): Show | 13 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+5754_110+5755d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162747 | ||||||
chr10:15162928
|
G | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+5575C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162928 | ||||||
chr10:15162930
|
T | G | 1 | a0001c0001t0008g0246 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.110+5573A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162930 | ||||||
chr10:15162973
|
C | T | 1 | a0001c0001t0030g0082 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.110+5530G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162973 | ||||||
chr10:15163058
|
C | T | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+5445G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163058 | ||||||
chr10:15163096
|
C | T | 33 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0267others(30): Show | 33 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.110+5407G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163096 | ||||||
chr10:15163322
|
A | T | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0008g0147others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+5181T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163322 | ||||||
chr10:15163353
|
G | A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110+5150C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163353 | ||||||
chr10:15163473
|
C | T | 54 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(51): Show | 54 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+5030G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163473 | ||||||
chr10:15163478
|
G | C | 2 | a0001c0002t0010g0090a0001c0005t0009g0128 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+5025C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163478 | ||||||
chr10:15163656
|
A | G | 29 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+4847T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163656 | ||||||
chr10:15163721
|
T | G | 132 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(129): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.110+4782A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163721 | ||||||
chr10:15163724
|
G | A | 72 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(69): Show | 72 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.110+4779C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163724 | ||||||
chr10:15163743
|
T | C | 62 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(59): Show | 62 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.110+4760A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163743 | ||||||
chr10:15163772
|
A | T | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+4731T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163772 | ||||||
chr10:15163773
|
C | A | 4 | a0001c0001t0004g0269a0001c0002t0018g0268a0001c0002t0018g0271others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+4730G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163773 | ||||||
chr10:15163813
|
T | C | 2 | a0001c0001t0003g0071a0001c0001t0003g0072 | 2 | HG00597.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.110+4690A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163813 | ||||||
chr10:15163824
|
T | C | 1 | a0001c0002t0032g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.110+4679A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163824 | ||||||
chr10:15163826
|
C | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0134others(7): Show | 10 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+4677G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163826 | ||||||
chr10:15163827
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.110+4676G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163827 | ||||||
chr10:15163909
|
G | A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110+4594C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163909 | ||||||
chr10:15163950
|
C | T | 5 | a0001c0001t0004g0269a0001c0001t0034g0098a0001c0002t0018g0268others(2): Show | 5 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+4553G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163950 | ||||||
chr10:15163975
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.110+4528C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163975 | ||||||
chr10:15163995
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+4508A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163995 | ||||||
chr10:15163996
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+4507C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163996 | ||||||
chr10:15164003
|
C | A | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+4500G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164003 | ||||||
chr10:15164049
|
G | A | 35 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.110+4454C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164049 | ||||||
chr10:15164132
|
G | A | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110+4371C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164132 | ||||||
chr10:15164182
|
C | CA | 21 | a0001c0001t0001g0004a0001c0001t0001g0132a0001c0001t0001g0135others(18): Show | 21 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.110+4320dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164182 | ||||||
chr10:15164182
|
CA | C | 54 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(51): Show | 54 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+4320delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164182 | ||||||
chr10:15164182
|
CAA | C | 70 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.110+4319_110+4320d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164182 | ||||||
chr10:15164269
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.110+4234T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164269 | ||||||
chr10:15164271
|
A | G | 1 | a0001c0001t0004g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110+4232T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164271 | ||||||
chr10:15164461
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.110+4042G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164461 | ||||||
chr10:15164516
|
G | A | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3987C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164516 | ||||||
chr10:15164518
|
T | A | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3985A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164518 | ||||||
chr10:15164726
|
G | A | 24 | a0001c0001t0001g0019a0001c0001t0001g0075a0001c0001t0001g0076others(21): Show | 24 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.110+3777C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164726 | ||||||
chr10:15164760
|
G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+3743C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164760 | ||||||
chr10:15164804
|
A | G | 108 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.110+3699T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164804 | ||||||
chr10:15164849
|
T | C | 7 | a0001c0001t0001g0091a0001c0001t0006g0127a0001c0002t0005g0276others(4): Show | 7 | HG01109.hp1 HG01975.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+3654A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164849 | ||||||
chr10:15164865
|
C | CTACTAAA others(4): Show |
30 | a0001c0001t0001g0019a0001c0001t0001g0075a0001c0001t0001g0076others(27): Show | 30 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.110+3627_110+3637d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164865 | ||||||
chr10:15164903
|
C | T | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+3600G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164903 | ||||||
chr10:15164992
|
T | C | 132 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(129): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.110+3511A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164992 | ||||||
chr10:15165024
|
G | A | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3479C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165024 | ||||||
chr10:15165035
|
C | T | 57 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(54): Show | 57 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.110+3468G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165035 | ||||||
chr10:15165094
|
T | C | 66 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(63): Show | 66 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.110+3409A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165094 | ||||||
chr10:15165098
|
G | A | 2 | a0001c0002t0010g0090a0001c0005t0009g0128 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+3405C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165098 | ||||||
chr10:15165109
|
G | A | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3394C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165109 | ||||||
chr10:15165163
|
C | CA | 33 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0091others(30): Show | 33 | HG00140.hp2 HG01192.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+3339dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165163 | ||||||
chr10:15165163
|
CA | C | 59 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(56): Show | 59 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.110+3339delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165163 | ||||||
chr10:15165178
|
A | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+3325T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165178 | ||||||
chr10:15165197
|
T | TC | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3305_110+3306i others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165197 | ||||||
chr10:15165370
|
G | T | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3133C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165370 | ||||||
chr10:15165395
|
G | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3108C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165395 | ||||||
chr10:15165435
|
A | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3068T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165435 | ||||||
chr10:15165455
|
A | G | 1 | a0001c0002t0015g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.110+3048T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165455 | ||||||
chr10:15165875
|
C | CA | 13 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0091others(10): Show | 13 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+2627dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | ||||||
chr10:15165875
|
C | CAA | 75 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(72): Show | 75 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.110+2626_110+2627d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | ||||||
chr10:15165875
|
CA | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0135a0001c0001t0006g0081others(7): Show | 10 | HG01192.hp2 HG01884.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+2627delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | ||||||
chr10:15165875
|
CAA | C | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2626_110+2627d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | ||||||
chr10:15166012
|
A | G | 43 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+2491T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166012 | ||||||
chr10:15166025
|
C | T | 28 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(25): Show | 28 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+2478G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166025 | ||||||
chr10:15166079
|
TA | T | 4 | a0001c0001t0001g0019a0001c0002t0002g0017a0001c0002t0012g0018others(1): Show | 4 | HG02809.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+2423delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166079 | ||||||
chr10:15166132
|
A | G | 9 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00438.hp2 HG01975.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+2371T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166132 | ||||||
chr10:15166232
|
T | A | 48 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(45): Show | 48 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.110+2271A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166232 | ||||||
chr10:15166284
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.110+2219G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166284 | ||||||
chr10:15166395
|
G | C | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.110+2108C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166395 | ||||||
chr10:15166442
|
C | CTACT | 6 | a0001c0002t0010g0011a0001c0002t0010g0012a0001c0006t0016g0010others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2057_110+2060d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166442 | ||||||
chr10:15166471
|
C | T | 1 | a0001c0001t0004g0002 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110+2032G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166471 | ||||||
chr10:15166473
|
A | G | 3 | a0001c0001t0011g0007a0001c0001t0011g0008a0001c0001t0011g0009 | 3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110+2030T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166473 | ||||||
chr10:15166617
|
T | C | 1 | a0001c0005t0003g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.110+1886A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166617 | ||||||
chr10:15166637
|
T | C | 2 | a0001c0002t0019g0130a0001c0002t0019g0131 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+1866A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166637 | ||||||
chr10:15167181
|
TAA | T | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(124): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.110+1320_110+1321d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167181 | ||||||
chr10:15167431
|
C | T | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(124): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.110+1072G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167431 | ||||||
chr10:15167571
|
A | C | 1 | a0001c0001t0053g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.110+932T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167571 | ||||||
chr10:15167959
|
C | G | 1 | a0001c0001t0005g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.110+544G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167959 | ||||||
chr10:15167991
|
G | A | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.110+512C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167991 | ||||||
chr10:15168101
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0009g0003 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.110+402G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15168101 | ||||||
chr10:15168244
|
G | T | 1 | a0001c0001t0004g0002 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110+259C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15168244 |