geneid | 64802 |
---|---|
ensemblid | ENSG00000173614.14 |
hgncid | 17877 |
symbol | NMNAT1 |
name | nicotinamide nucleotide adenylyltransferase 1 |
refseq_nuc | NM_022787.4 |
refseq_prot | NP_073624.2 |
ensembl_nuc | ENST00000377205.6 |
ensembl_prot | ENSP00000366410.1 |
mane_status | MANE Select |
chr | chr1 |
start | 9943475 |
end | 9985498 |
strand | + |
ver | v1.2 |
region | chr1:9943475-9985498 |
region5000 | chr1:9938475-9990498 |
regionname0 | NMNAT1_chr1_9943475_9985498 |
regionname5000 | NMNAT1_chr1_9938475_9990498 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 279 | 308 | 87 | 52 | 117 | 6 | 44 | 90 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0002 | 0/0 | 279 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0003 | 0/0 | 279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0004 | 0/0 | 279 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 840 | 308 | 87 | 52 | 117 | 6 | 44 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
c0002 | 0/0 | 840 | 4 | 0 | 0 | 4 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
c0003 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
c0004 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2895 | 74 | 5 | 20 | 27 | 4 | 17 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0002 | 0/0 | 2896 | 74 | 22 | 7 | 27 | 1 | 17 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0003 | 0/0 | 2895 | 56 | 8 | 10 | 34 | 0 | 4 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0004 | 1/0 | 2895 | 26 | 22 | 2 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0005 | 0/0 | 2895 | 20 | 0 | 1 | 19 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0006 | 0/0 | 2894 | 17 | 0 | 6 | 10 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0007 | 0/0 | 2895 | 7 | 6 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0008 | 0/0 | 2895 | 6 | 6 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0009 | 0/0 | 2896 | 5 | 5 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0010 | 0/0 | 2895 | 5 | 1 | 3 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0011 | 0/0 | 2895 | 3 | 0 | 0 | 0 | 0 | 3 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0012 | 0/0 | 2896 | 3 | 3 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0013 | 0/0 | 2895 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0014 | 0/0 | 2896 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0015 | 0/0 | 2895 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0016 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0017 | 0/0 | 2896 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0018 | 0/0 | 2896 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0019 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0020 | 0/0 | 2896 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0021 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0022 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0023 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0024 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0025 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0026 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
t0027 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 2 | 1 | 2 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 840 | 308 | 87 | 52 | 117 | 6 | 44 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0002c0002 | 0/0 | 840 | 4 | 0 | 0 | 4 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0003c0003 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0004c0004 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3734 | 73 | 5 | 20 | 26 | 4 | 17 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0002 | 0/0 | 3735 | 74 | 22 | 7 | 27 | 1 | 17 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0003 | 0/0 | 3734 | 52 | 8 | 10 | 30 | 0 | 4 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0004 | 1/0 | 3734 | 26 | 22 | 2 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0005 | 0/0 | 3734 | 20 | 0 | 1 | 19 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0006 | 0/0 | 3733 | 17 | 0 | 6 | 10 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0007 | 0/0 | 3734 | 7 | 6 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0008 | 0/0 | 3734 | 6 | 6 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0009 | 0/0 | 3735 | 5 | 5 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0010 | 0/0 | 3734 | 5 | 1 | 3 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0011 | 0/0 | 3734 | 3 | 0 | 0 | 0 | 0 | 3 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0012 | 0/0 | 3735 | 3 | 3 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0013 | 0/0 | 3734 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0014 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0015 | 0/0 | 3734 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0016 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0017 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0018 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0019 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0020 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0022 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0023 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0024 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0025 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0026 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0001c0001t0027 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0002c0002t0003 | 0/0 | 3734 | 4 | 0 | 0 | 4 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0003c0003t0021 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
a0004c0004t0001 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | copy fasta | chr1 | 9938475 | 9990498 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0001 | 0/0 | 6 | 2 | 1 | 2 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0010g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0010g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0011g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0013g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0015g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0016g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0017g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0019g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0020g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0022g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0026g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0001c0001t0027g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0003c0003t0021g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0010 | g0021 | EUR | GBR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | FIN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0280 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00558 | hp1 | a0004 | c0004 | t0001 | g0239 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0281 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0085 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01256 | hp1 | a0001 | c0001 | t0010 | g0169 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01258 | hp1 | a0001 | c0001 | t0010 | g0170 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01361 | hp2 | a0001 | c0001 | t0025 | g0201 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0288 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01433 | hp2 | a0001 | c0001 | t0020 | g0026 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0083 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0275 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0250 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0276 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0284 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02004 | hp1 | a0001 | c0001 | t0010 | g0171 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0086 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0273 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0277 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | CDX | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0287 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02451 | hp2 | a0001 | c0001 | t0027 | g0015 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02572 | hp1 | a0001 | c0001 | t0024 | g0088 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0082 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02723 | hp2 | a0001 | c0001 | t0022 | g0064 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03017 | hp1 | a0001 | c0001 | t0011 | g0226 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0174 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0018 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0016 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03225 | hp2 | a0001 | c0001 | t0019 | g0291 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03491 | hp2 | a0001 | c0001 | t0011 | g0227 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03492 | hp2 | a0001 | c0001 | t0011 | g0228 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0289 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04184 | hp2 | a0001 | c0001 | t0017 | g0215 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04228 | hp1 | a0001 | c0001 | t0016 | g0243 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0278 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18906 | hp2 | a0001 | c0001 | t0026 | g0027 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18946 | hp1 | a0001 | c0001 | t0006 | g0286 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18951 | hp1 | a0001 | c0001 | t0023 | g0002 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18967 | hp2 | a0001 | c0001 | t0013 | g0045 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18972 | hp2 | a0001 | c0001 | t0018 | g0069 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18983 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18989 | hp2 | a0002 | c0002 | t0003 | g0035 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19005 | hp1 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19012 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19057 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19067 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19068 | hp1 | a0001 | c0001 | t0013 | g0042 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19072 | hp1 | a0001 | c0001 | t0006 | g0274 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ASW | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | TSI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | GIH | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | GIH | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02109 | hp1 | a0003 | c0003 | t0021 | g0014 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA20300 | hp2 | a0001 | c0001 | t0010 | g0172 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0194 | REF | REF | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0146 | REF | REF | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9972091
|
G | T | 1 | a0004 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.18G>T | p.Lys6Asn | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/5 | 115/3734 | 18/840 | 6/279 | chr1 | 9972091 | ||
chr1:9972096
|
A | C | 1 | a0003 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.23A>C | p.Glu8Ala | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/5 | 120/3734 | 23/840 | 8/279 | chr1 | 9972096 | ||
chr1:9982625
|
G | A | 1 | a0002 | 4 | NA18983.hp2 NA18989.hp2 NA18992.hp2 others(1): Show |
missense_variant | MODERATE | c.764G>A | p.Ser255Asn | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 861/3734 | 764/840 | 255/279 | chr1 | 9982625 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9943481
|
C | T | 1 | a0001c0001t0027 | 1 | HG02451.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/5 | chr1 | 9943481 | ||||||
chr1:9982717
|
A | G | 1 | a0001c0001t0026 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 16 | chr1 | 9982717 | |||||
chr1:9982846
|
G | A | 1 | a0001c0001t0013 | 2 | NA18967.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*145G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 145 | chr1 | 9982846 | |||||
chr1:9982903
|
C | T | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 202 | chr1 | 9982903 | |||||
chr1:9983053
|
C | T | 2 | a0001c0001t0007a0001c0001t0024 | 8 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 352 | chr1 | 9983053 | |||||
chr1:9983084
|
G | A | 8 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(5): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*383G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 383 | chr1 | 9983084 | |||||
chr1:9983104
|
C | CA | 5 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(2): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*418dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 419 | INFO_REALIGN_3_PRIME | chr1 | 9983104 | ||||
chr1:9983104
|
CA | C | 2 | a0001c0001t0006a0001c0001t0008 | 23 | HG00408.hp1 HG00558.hp2 HG01433.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*418delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 418 | INFO_REALIGN_3_PRIME | chr1 | 9983104 | ||||
chr1:9983226
|
A | G | 1 | a0001c0001t0009 | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 525 | chr1 | 9983226 | |||||
chr1:9983246
|
T | G | 1 | a0001c0001t0016 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 545 | chr1 | 9983246 | |||||
chr1:9983308
|
T | G | 1 | a0001c0001t0015 | 2 | HG01884.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*607T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 607 | chr1 | 9983308 | |||||
chr1:9983358
|
G | A | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(19): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*657G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 657 | chr1 | 9983358 | |||||
chr1:9983400
|
A | G | 9 | a0001c0001t0003a0001c0001t0013a0001c0001t0018others(6): Show | 64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*699A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 699 | chr1 | 9983400 | |||||
chr1:9983635
|
G | A | 1 | a0001c0001t0024 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*934G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 934 | chr1 | 9983635 | |||||
chr1:9983655
|
C | CA | 3 | a0001c0001t0008a0001c0001t0017a0001c0001t0020 | 8 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*968dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 969 | INFO_REALIGN_3_PRIME | chr1 | 9983655 | ||||
chr1:9983764
|
G | C | 1 | a0001c0001t0010 | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1063 | chr1 | 9983764 | |||||
chr1:9983764
|
G | T | 1 | a0001c0001t0005 | 20 | HG00597.hp1 HG00597.hp2 HG01943.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1063 | chr1 | 9983764 | |||||
chr1:9983782
|
G | T | 2 | a0001c0001t0010a0001c0001t0019 | 6 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1081G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1081 | chr1 | 9983782 | |||||
chr1:9983847
|
C | T | 1 | a0001c0001t0019 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1146C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1146 | chr1 | 9983847 | |||||
chr1:9984204
|
T | C | 1 | a0001c0001t0014 | 2 | HG03225.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1503T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1503 | chr1 | 9984204 | |||||
chr1:9984390
|
A | AAGAACAA others(11): Show |
1 | a0001c0001t0027 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1701_*1718dupTGTA others(14): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1719 | INFO_REALIGN_3_PRIME | chr1 | 9984390 | ||||
chr1:9985094
|
C | G | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(19): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2393C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2393 | chr1 | 9985094 | |||||
chr1:9985160
|
C | T | 1 | a0001c0001t0023 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2459 | chr1 | 9985160 | |||||
chr1:9985223
|
A | T | 1 | a0001c0001t0022 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2522 | chr1 | 9985223 | |||||
chr1:9985232
|
G | A | 1 | a0001c0001t0011 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2531G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2531 | chr1 | 9985232 | |||||
chr1:9985240
|
A | T | 1 | a0003c0003t0021 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2539A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2539 | chr1 | 9985240 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:9943750
|
C | A | 2 | a0001c0001t0027g0015a0003c0003t0021g0014 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-57+235C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9943750 | ||||||
chr1:9943897
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-57+382C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9943897 | ||||||
chr1:9944014
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+499G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944014 | ||||||
chr1:9944026
|
A | G | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+511A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944026 | ||||||
chr1:9944030
|
G | A | 1 | a0001c0001t0010g0021 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-57+515G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944030 | ||||||
chr1:9944247
|
C | T | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+732C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944247 | ||||||
chr1:9944285
|
C | T | 1 | a0001c0001t0004g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+770C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944285 | ||||||
chr1:9944289
|
C | T | 17 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(14): Show | 17 | HG00408.hp1 HG00558.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+774C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944289 | ||||||
chr1:9944292
|
G | A | 57 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(54): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+777G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944292 | ||||||
chr1:9944293
|
G | T | 1 | a0001c0001t0002g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-57+778G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944293 | ||||||
chr1:9944550
|
G | A | 57 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(54): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+1035G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944550 | ||||||
chr1:9944816
|
C | CAGAGTTA others(9): Show |
1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+1302_-57+1317d others(18): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9944816 | |||||
chr1:9944824
|
C | T | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-57+1309C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944824 | ||||||
chr1:9944979
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+1464A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944979 | ||||||
chr1:9945048
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-57+1533A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945048 | ||||||
chr1:9945238
|
AC | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+1724delC | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945238 | ||||||
chr1:9945817
|
G | A | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+2302G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945817 | ||||||
chr1:9945936
|
T | C | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+2421T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945936 | ||||||
chr1:9946013
|
C | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+2498C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946013 | ||||||
chr1:9946320
|
C | T | 1 | a0001c0001t0004g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+2805C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946320 | ||||||
chr1:9946342
|
T | G | 1 | a0001c0001t0006g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57+2827T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946342 | ||||||
chr1:9946434
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+2919A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946434 | ||||||
chr1:9946435
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+2920G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946435 | ||||||
chr1:9946514
|
T | A | 1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+2999T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946514 | ||||||
chr1:9946705
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+3190A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946705 | ||||||
chr1:9946724
|
A | T | 2 | a0001c0001t0005g0270a0001c0001t0005g0271 | 2 | NA18974.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-57+3209A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946724 | ||||||
chr1:9947291
|
G | A | 16 | a0001c0001t0004g0006a0001c0001t0004g0079a0001c0001t0004g0080others(13): Show | 17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+3776G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947291 | ||||||
chr1:9947376
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-57+3861C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947376 | ||||||
chr1:9947470
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+3955A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947470 | ||||||
chr1:9947638
|
T | G | 4 | a0001c0001t0007g0075a0001c0001t0007g0076a0001c0001t0007g0077others(1): Show | 4 | HG02717.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4123T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947638 | ||||||
chr1:9947704
|
C | T | 1 | a0001c0001t0006g0289 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-57+4189C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947704 | ||||||
chr1:9947765
|
T | G | 2 | a0001c0001t0010g0169a0001c0001t0010g0170 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-57+4250T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947765 | ||||||
chr1:9947789
|
G | T | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | NA18970.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-57+4274G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947789 | ||||||
chr1:9947955
|
G | T | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4440G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947955 | ||||||
chr1:9948098
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+4583A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948098 | ||||||
chr1:9948133
|
G | A | 57 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(54): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+4618G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948133 | ||||||
chr1:9948163
|
G | A | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-57+4648G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948163 | ||||||
chr1:9948242
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-57+4727C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948242 | ||||||
chr1:9948307
|
G | T | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4792G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948307 | ||||||
chr1:9948372
|
C | T | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-57+4857C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948372 | ||||||
chr1:9948468
|
T | C | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4953T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948468 | ||||||
chr1:9948505
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+4990C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948505 | ||||||
chr1:9948560
|
C | T | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+5045C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948560 | ||||||
chr1:9948605
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-57+5090T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948605 | ||||||
chr1:9948651
|
A | AT | 18 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0003g0003others(15): Show | 23 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+5151dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9948651 | |||||
chr1:9948710
|
C | G | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+5195C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948710 | ||||||
chr1:9948710
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-57+5195C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948710 | ||||||
chr1:9948802
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-57+5287A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948802 | ||||||
chr1:9948868
|
G | A | 6 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+5353G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948868 | ||||||
chr1:9948947
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | NA18977.hp1 NA18989.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-57+5432C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948947 | ||||||
chr1:9949056
|
C | T | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-57+5541C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949056 | ||||||
chr1:9949080
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-57+5565A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949080 | ||||||
chr1:9949150
|
A | G | 1 | a0001c0001t0004g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57+5635A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949150 | ||||||
chr1:9949160
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-57+5645C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949160 | ||||||
chr1:9949161
|
G | A | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+5646G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949161 | ||||||
chr1:9949294
|
C | T | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57+5779C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949294 | ||||||
chr1:9949349
|
A | G | 3 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0059 | 3 | HG00408.hp2 HG02165.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-57+5834A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949349 | ||||||
chr1:9949410
|
C | CT | 40 | a0001c0001t0002g0159a0001c0001t0002g0165a0001c0001t0003g0002others(37): Show | 42 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+5912dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949410 | |||||
chr1:9949410
|
C | CTTT | 112 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(109): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-57+5910_-57+5912d others(5): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949410 | |||||
chr1:9949410
|
C | CTTTT | 8 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0005g0258others(5): Show | 8 | HG00597.hp1 HG00597.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+5909_-57+5912d others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949410 | |||||
chr1:9949534
|
C | T | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+6019C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949534 | ||||||
chr1:9949535
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-57+6020G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949535 | ||||||
chr1:9949580
|
T | TTG | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-57+6073_-57+6074d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949580 | |||||
chr1:9949588
|
G | GTA | 57 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(54): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+6085_-57+6086d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949588 | |||||
chr1:9949804
|
A | G | 2 | a0001c0001t0005g0257a0001c0001t0005g0263 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+6289A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949804 | ||||||
chr1:9949867
|
T | C | 55 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(52): Show | 63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-57+6352T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949867 | ||||||
chr1:9949956
|
A | G | 1 | a0001c0001t0002g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-57+6441A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949956 | ||||||
chr1:9950286
|
T | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(84): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-57+6771T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950286 | ||||||
chr1:9950338
|
G | A | 1 | a0001c0001t0004g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57+6823G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950338 | ||||||
chr1:9950554
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57+7039A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950554 | ||||||
chr1:9950784
|
C | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7269C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950784 | ||||||
chr1:9950827
|
A | G | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-57+7312A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950827 | ||||||
chr1:9950897
|
T | G | 28 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0036others(25): Show | 30 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+7382T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950897 | ||||||
chr1:9950920
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+7405C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950920 | ||||||
chr1:9951013
|
C | A | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-57+7498C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951013 | ||||||
chr1:9951047
|
C | T | 8 | a0001c0001t0007g0075a0001c0001t0007g0076a0001c0001t0007g0077others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+7532C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951047 | ||||||
chr1:9951054
|
A | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(84): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-57+7539A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951054 | ||||||
chr1:9951088
|
CA | C | 19 | a0001c0001t0001g0178a0001c0001t0001g0251a0001c0001t0001g0252others(16): Show | 19 | HG01884.hp2 HG02165.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.-57+7589delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9951088 | |||||
chr1:9951107
|
G | A | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG02895.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-57+7592G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951107 | ||||||
chr1:9951108
|
G | A | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG02895.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-57+7593G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951108 | ||||||
chr1:9951462
|
T | G | 73 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(70): Show | 83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-57+7947T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951462 | ||||||
chr1:9951465
|
G | T | 29 | a0001c0001t0002g0010a0001c0001t0002g0091a0001c0001t0002g0092others(26): Show | 30 | HG01167.hp2 HG01943.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+7950G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951465 | ||||||
chr1:9951476
|
T | C | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | NA18970.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-57+7961T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951476 | ||||||
chr1:9951477
|
G | GTTGT | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-57+7973_-57+7976d others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9951477 | |||||
chr1:9951621
|
C | T | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+8106C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951621 | ||||||
chr1:9951713
|
G | T | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+8198G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951713 | ||||||
chr1:9951912
|
A | G | 1 | a0001c0001t0004g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+8397A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951912 | ||||||
chr1:9952088
|
G | A | 57 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(54): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+8573G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952088 | ||||||
chr1:9952134
|
T | TA | 29 | a0001c0001t0002g0074a0001c0001t0003g0002a0001c0001t0003g0022others(26): Show | 31 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+8628dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9952134 | |||||
chr1:9952149
|
A | T | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+8634A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952149 | ||||||
chr1:9952207
|
C | T | 2 | a0001c0001t0005g0257a0001c0001t0005g0263 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+8692C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952207 | ||||||
chr1:9952253
|
G | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+8738G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952253 | ||||||
chr1:9952582
|
G | T | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+9067G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952582 | ||||||
chr1:9952819
|
G | A | 1 | a0001c0001t0005g0246 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-57+9304G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952819 | ||||||
chr1:9952834
|
C | T | 7 | a0001c0001t0002g0009a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 8 | HG02698.hp2 HG03490.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+9319C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952834 | ||||||
chr1:9952860
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+9345C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952860 | ||||||
chr1:9952956
|
A | C | 68 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(65): Show | 76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-57+9441A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952956 | ||||||
chr1:9953003
|
C | T | 2 | a0001c0001t0015g0082a0001c0001t0015g0083 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-57+9488C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953003 | ||||||
chr1:9953020
|
G | A | 2 | a0001c0001t0010g0169a0001c0001t0010g0170 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-57+9505G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953020 | ||||||
chr1:9953137
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-57+9622C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953137 | ||||||
chr1:9953278
|
C | CT | 23 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(20): Show | 23 | HG00423.hp1 HG00597.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+9780dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953278 | |||||
chr1:9953278
|
CT | C | 36 | a0001c0001t0001g0179a0001c0001t0002g0009a0001c0001t0002g0010others(33): Show | 40 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.-57+9780delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953278 | |||||
chr1:9953327
|
A | G | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+9812A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953327 | ||||||
chr1:9953448
|
G | GT | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-57+9944dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953448 | |||||
chr1:9953448
|
G | GTT | 7 | a0001c0001t0005g0271a0001c0001t0006g0284a0001c0001t0008g0173others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+9943_-57+9944d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953448 | |||||
chr1:9953509
|
C | T | 1 | a0004c0004t0001g0239 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-57+9994C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953509 | ||||||
chr1:9953533
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-57+10018C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953533 | ||||||
chr1:9953667
|
G | A | 5 | a0001c0001t0005g0247a0001c0001t0005g0248a0001c0001t0005g0256others(2): Show | 5 | NA18951.hp2 NA18959.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+10152G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953667 | ||||||
chr1:9953797
|
C | CT | 19 | a0001c0001t0002g0074a0001c0001t0002g0090a0001c0001t0002g0102others(16): Show | 19 | HG00438.hp2 HG01981.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57+10308dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | |||||
chr1:9953797
|
CT | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0237a0001c0001t0001g0238others(17): Show | 21 | HG00099.hp1 HG00597.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57+10308delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | |||||
chr1:9953797
|
CTT | C | 156 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0178others(153): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-57+10307_-57+1030 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | |||||
chr1:9953797
|
CTTT | C | 6 | a0001c0001t0001g0180a0001c0001t0003g0036a0001c0001t0003g0054others(3): Show | 6 | HG00423.hp1 HG00558.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+10306_-57+1030 others(7): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | |||||
chr1:9953797
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-57+10299_-57+1030 others(14): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | |||||
chr1:9954009
|
T | G | 1 | a0001c0001t0006g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57+10494T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954009 | ||||||
chr1:9954025
|
T | G | 1 | a0001c0001t0005g0181 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-57+10510T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954025 | ||||||
chr1:9954115
|
C | G | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+10600C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954115 | ||||||
chr1:9954121
|
A | G | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+10606A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954121 | ||||||
chr1:9954283
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-57+10768C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954283 | ||||||
chr1:9954328
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-57+10813A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954328 | ||||||
chr1:9954376
|
ACTT | A | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+10867_-57+1086 others(7): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9954376 | |||||
chr1:9954489
|
A | G | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+10974A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954489 | ||||||
chr1:9954620
|
C | T | 27 | a0001c0001t0002g0009a0001c0001t0002g0094a0001c0001t0002g0095others(24): Show | 30 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+11105C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954620 | ||||||
chr1:9954789
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57+11274C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954789 | ||||||
chr1:9954799
|
C | T | 2 | a0001c0001t0027g0015a0003c0003t0021g0014 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-57+11284C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954799 | ||||||
chr1:9954802
|
G | A | 6 | a0001c0001t0003g0053a0001c0001t0010g0021a0001c0001t0010g0169others(3): Show | 6 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+11287G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954802 | ||||||
chr1:9954929
|
CA | C | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-57+11428delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9954929 | |||||
chr1:9955129
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+11614G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955129 | ||||||
chr1:9955369
|
A | G | 28 | a0001c0001t0003g0002a0001c0001t0003g0022a0001c0001t0003g0036others(25): Show | 30 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+11854A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955369 | ||||||
chr1:9955403
|
C | CA | 6 | a0001c0001t0002g0074a0001c0001t0002g0126a0001c0001t0002g0168others(3): Show | 6 | HG01981.hp2 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+11907dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | |||||
chr1:9955403
|
C | CAA | 71 | a0001c0001t0001g0029a0001c0001t0001g0232a0001c0001t0001g0233others(68): Show | 79 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-57+11906_-57+1190 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | |||||
chr1:9955403
|
C | CAAA | 96 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(93): Show | 98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-57+11905_-57+1190 others(7): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | |||||
chr1:9955403
|
C | CAAAA | 18 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(15): Show | 18 | HG00597.hp2 HG01123.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+11904_-57+1190 others(8): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | |||||
chr1:9955418
|
A | C | 1 | a0001c0001t0004g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57+11903A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955418 | ||||||
chr1:9955474
|
G | A | 8 | a0001c0001t0007g0075a0001c0001t0007g0076a0001c0001t0007g0077others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+11959G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955474 | ||||||
chr1:9955504
|
C | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0032others(13): Show | 21 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-57+11989C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955504 | ||||||
chr1:9955640
|
C | T | 63 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(60): Show | 71 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+12125C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955640 | ||||||
chr1:9955765
|
G | A | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12250G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955765 | ||||||
chr1:9956104
|
A | G | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12589A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956104 | ||||||
chr1:9956170
|
C | CT | 7 | a0001c0001t0003g0050a0001c0001t0005g0245a0001c0001t0008g0173others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+12672dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956170 | |||||
chr1:9956172
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57+12657T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956172 | ||||||
chr1:9956175
|
T | C | 1 | a0001c0001t0004g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57+12660T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956175 | ||||||
chr1:9956232
|
C | T | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+12717C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956232 | ||||||
chr1:9956236
|
C | G | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12721C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956236 | ||||||
chr1:9956277
|
C | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0179a0001c0001t0001g0182others(11): Show | 15 | HG00099.hp2 HG00639.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57+12762C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956277 | ||||||
chr1:9956420
|
C | CT | 60 | a0001c0001t0001g0029a0001c0001t0001g0182a0001c0001t0001g0235others(57): Show | 68 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-57+12924dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956420 | |||||
chr1:9956420
|
CT | C | 90 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0199others(87): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-57+12924delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956420 | |||||
chr1:9956510
|
C | T | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57+12995C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956510 | ||||||
chr1:9956707
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-57+13192G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956707 | ||||||
chr1:9956731
|
C | CT | 15 | a0001c0001t0001g0179a0001c0001t0001g0196a0001c0001t0001g0197others(12): Show | 17 | HG00099.hp2 HG00597.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+13234dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956731 | |||||
chr1:9956731
|
C | CTT | 6 | a0001c0001t0001g0189a0001c0001t0010g0021a0001c0001t0010g0169others(3): Show | 6 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+13233_-57+1323 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956731 | |||||
chr1:9956835
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-57+13320G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956835 | ||||||
chr1:9956845
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-57+13330C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956845 | ||||||
chr1:9956871
|
G | A | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-57+13356G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956871 | ||||||
chr1:9956928
|
C | T | 1 | a0001c0001t0005g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57+13413C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956928 | ||||||
chr1:9956976
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-57+13461C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956976 | ||||||
chr1:9957028
|
C | T | 2 | a0001c0001t0015g0082a0001c0001t0015g0083 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-57+13513C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957028 | ||||||
chr1:9957059
|
C | T | 1 | a0001c0001t0005g0231 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-57+13544C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957059 | ||||||
chr1:9957161
|
C | A | 1 | a0001c0001t0008g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57+13646C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957161 | ||||||
chr1:9957217
|
C | T | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+13702C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957217 | ||||||
chr1:9957359
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57+13844C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957359 | ||||||
chr1:9957469
|
G | A | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+13954G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957469 | ||||||
chr1:9957591
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57+14076C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957591 | ||||||
chr1:9957828
|
C | G | 1 | a0001c0001t0002g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-14190C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957828 | ||||||
chr1:9957836
|
G | A | 1 | a0001c0001t0004g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-56-14182G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957836 | ||||||
chr1:9957933
|
C | T | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-14085C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957933 | ||||||
chr1:9958144
|
A | G | 5 | a0001c0001t0008g0173a0001c0001t0008g0174a0001c0001t0008g0175others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-13874A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958144 | ||||||
chr1:9958443
|
G | GT | 7 | a0001c0001t0001g0230a0001c0001t0003g0036a0001c0001t0003g0038others(4): Show | 7 | HG00544.hp1 HG01192.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-13561dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9958443 | |||||
chr1:9958443
|
GT | G | 8 | a0001c0001t0001g0182a0001c0001t0003g0040a0001c0001t0006g0286others(5): Show | 8 | HG02135.hp1 HG02922.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-13561delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9958443 | |||||
chr1:9958448
|
T | G | 43 | a0001c0001t0001g0203a0001c0001t0002g0001a0001c0001t0002g0074others(40): Show | 48 | HG00423.hp2 HG00741.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-56-13570T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958448 | ||||||
chr1:9958453
|
T | G | 2 | a0001c0001t0002g0115a0001c0001t0019g0291 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-13565T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958453 | ||||||
chr1:9958483
|
A | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(84): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56-13535A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958483 | ||||||
chr1:9958502
|
T | C | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-56-13516T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958502 | ||||||
chr1:9958591
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-56-13427C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958591 | ||||||
chr1:9958655
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-56-13363G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958655 | ||||||
chr1:9958685
|
A | G | 284 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(281): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-56-13333A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958685 | ||||||
chr1:9959071
|
T | C | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-12947T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959071 | ||||||
chr1:9959201
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-56-12817A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959201 | ||||||
chr1:9959296
|
C | T | 3 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-56-12722C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959296 | ||||||
chr1:9959297
|
G | T | 1 | a0001c0001t0002g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-56-12721G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959297 | ||||||
chr1:9959320
|
T | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0091a0001c0001t0002g0092others(6): Show | 10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-12698T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959320 | ||||||
chr1:9959327
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-56-12691G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959327 | ||||||
chr1:9959373
|
GAAAAAA | G | 14 | a0001c0001t0002g0104a0001c0001t0002g0126a0001c0001t0002g0127others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-12625_-56-1262 others(10): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9959373 | |||||
chr1:9959373
|
GAAAAAAA | G | 254 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(251): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-56-12626_-56-1262 others(11): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9959373 | |||||
chr1:9959373
|
GAAAAAAA others(1): Show |
G | 8 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0093others(5): Show | 8 | HG02004.hp2 HG02451.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-12627_-56-1262 others(12): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9959373 | |||||
chr1:9959421
|
G | A | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-56-12597G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959421 | ||||||
chr1:9959534
|
A | T | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-12484A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959534 | ||||||
chr1:9959639
|
C | T | 3 | a0001c0001t0009g0007a0001c0001t0009g0008a0001c0001t0009g0138 | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-12379C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959639 | ||||||
chr1:9959876
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-56-12142T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959876 | ||||||
chr1:9960288
|
AAAAAACA others(5): Show |
A | 55 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(52): Show | 63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-56-11718_-56-1170 others(16): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9960288 | |||||
chr1:9960295
|
AAAAACAA others(4): Show |
A | 1 | a0001c0001t0003g0036 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-56-11718_-56-1170 others(15): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9960295 | |||||
chr1:9960836
|
T | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-11182T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9960836 | ||||||
chr1:9960844
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-56-11174G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9960844 | ||||||
chr1:9960881
|
G | A | 2 | a0001c0001t0004g0084a0001c0001t0004g0089 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-11137G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9960881 | ||||||
chr1:9961083
|
G | C | 1 | a0001c0001t0004g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-56-10935G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961083 | ||||||
chr1:9961332
|
CTT | C | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-10685_-56-1068 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961332 | ||||||
chr1:9961600
|
T | A | 1 | a0001c0001t0004g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-56-10418T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961600 | ||||||
chr1:9961823
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-56-10195G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961823 | ||||||
chr1:9961828
|
A | C | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-56-10190A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961828 | ||||||
chr1:9962020
|
G | C | 1 | a0001c0001t0003g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-9998G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962020 | ||||||
chr1:9962042
|
A | G | 27 | a0001c0001t0002g0009a0001c0001t0002g0094a0001c0001t0002g0095others(24): Show | 30 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-56-9976A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962042 | ||||||
chr1:9962064
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-9954G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962064 | ||||||
chr1:9962225
|
A | G | 1 | a0001c0001t0006g0284 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-56-9793A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962225 | ||||||
chr1:9962238
|
T | C | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-9780T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962238 | ||||||
chr1:9962481
|
GA | G | 34 | a0001c0001t0002g0001a0001c0001t0002g0074a0001c0001t0002g0090others(31): Show | 39 | HG00423.hp2 HG00741.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-9522delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962481 | |||||
chr1:9962497
|
T | A | 1 | a0001c0001t0003g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-56-9521T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962497 | ||||||
chr1:9962552
|
A | G | 1 | a0001c0001t0027g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-56-9466A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962552 | ||||||
chr1:9962677
|
G | GT | 80 | a0001c0001t0001g0013a0001c0001t0001g0178a0001c0001t0001g0179others(77): Show | 81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-56-9319dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962677 | |||||
chr1:9962677
|
G | GTT | 49 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0187others(46): Show | 49 | HG00597.hp1 HG00597.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-56-9320_-56-9319d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962677 | |||||
chr1:9962677
|
GT | G | 81 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 96 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.-56-9319delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962677 | |||||
chr1:9962976
|
T | C | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-9042T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962976 | ||||||
chr1:9963137
|
G | C | 55 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(52): Show | 63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-56-8881G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963137 | ||||||
chr1:9963235
|
T | C | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-56-8783T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963235 | ||||||
chr1:9963333
|
C | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-8685C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963333 | ||||||
chr1:9963643
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0032others(13): Show | 21 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-8375G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963643 | ||||||
chr1:9963694
|
A | C | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-8324A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963694 | ||||||
chr1:9963696
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | NA18943.hp1 NA18950.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-56-8322C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963696 | ||||||
chr1:9963792
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56-8226C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963792 | ||||||
chr1:9963830
|
T | C | 1 | a0001c0001t0006g0289 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-56-8188T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963830 | ||||||
chr1:9964107
|
G | T | 1 | a0001c0001t0002g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-56-7911G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964107 | ||||||
chr1:9964144
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-7874G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964144 | ||||||
chr1:9964196
|
G | A | 1 | a0001c0001t0005g0258 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-56-7822G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964196 | ||||||
chr1:9964206
|
A | G | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-7812A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964206 | ||||||
chr1:9964219
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0003g0037 | 2 | NA18988.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-56-7799G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964219 | ||||||
chr1:9964230
|
C | G | 16 | a0001c0001t0004g0006a0001c0001t0004g0079a0001c0001t0004g0080others(13): Show | 17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-56-7788C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964230 | ||||||
chr1:9964444
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-56-7574C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964444 | ||||||
chr1:9964495
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-7523G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964495 | ||||||
chr1:9964724
|
G | A | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-7294G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964724 | ||||||
chr1:9964821
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-7197A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964821 | ||||||
chr1:9964929
|
C | CA | 57 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0188others(54): Show | 61 | HG00099.hp1 HG00438.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.-56-7069dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9964929 | |||||
chr1:9964929
|
CA | C | 9 | a0001c0001t0001g0179a0001c0001t0003g0047a0001c0001t0004g0089others(6): Show | 9 | HG01070.hp2 HG02559.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-7069delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9964929 | |||||
chr1:9965024
|
T | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(84): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56-6994T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965024 | ||||||
chr1:9965185
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-56-6833C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965185 | ||||||
chr1:9965189
|
G | C | 187 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(184): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-6829G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965189 | ||||||
chr1:9965189
|
G | T | 1 | a0001c0001t0005g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-56-6829G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965189 | ||||||
chr1:9965190
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-56-6828G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965190 | ||||||
chr1:9965206
|
G | A | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-6812G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965206 | ||||||
chr1:9965315
|
C | CA | 21 | a0001c0001t0001g0241a0001c0001t0001g0266a0001c0001t0002g0105others(18): Show | 21 | HG01175.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-6684dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9965315 | |||||
chr1:9965369
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-56-6649G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965369 | ||||||
chr1:9965375
|
T | A | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-56-6643T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965375 | ||||||
chr1:9965517
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0238 | 2 | HG01081.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-56-6501C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965517 | ||||||
chr1:9965553
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0102a0001c0001t0002g0139 | 3 | HG00438.hp2 HG00544.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-56-6465G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965553 | ||||||
chr1:9965730
|
C | T | 27 | a0001c0001t0002g0009a0001c0001t0002g0094a0001c0001t0002g0095others(24): Show | 30 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-56-6288C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965730 | ||||||
chr1:9965816
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-56-6202G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965816 | ||||||
chr1:9965926
|
T | C | 34 | a0001c0001t0002g0001a0001c0001t0002g0074a0001c0001t0002g0090others(31): Show | 39 | HG00423.hp2 HG00741.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-6092T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965926 | ||||||
chr1:9965987
|
CA | C | 6 | a0001c0001t0002g0094a0001c0001t0002g0163a0001c0001t0006g0274others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-6020delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9965987 | |||||
chr1:9965998
|
A | T | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-6020A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965998 | ||||||
chr1:9965999
|
T | A | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-6019T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965999 | ||||||
chr1:9966248
|
G | A | 1 | a0001c0001t0022g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-56-5770G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9966248 | ||||||
chr1:9966339
|
G | A | 8 | a0001c0001t0001g0187a0001c0001t0001g0207a0001c0001t0001g0229others(5): Show | 8 | HG00280.hp2 HG02293.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-5679G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9966339 | ||||||
chr1:9966365
|
C | T | 2 | a0001c0001t0015g0082a0001c0001t0015g0083 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-56-5653C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9966365 | ||||||
chr1:9966612
|
CA | C | 269 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(266): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-56-5396delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9966612 | |||||
chr1:9966612
|
CAA | C | 7 | a0001c0001t0003g0038a0001c0001t0003g0043a0001c0001t0003g0049others(4): Show | 7 | HG00408.hp2 HG00544.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-5397_-56-5396d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9966612 | |||||
chr1:9967006
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-56-5012C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967006 | ||||||
chr1:9967130
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-56-4888A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967130 | ||||||
chr1:9967226
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-56-4792C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967226 | ||||||
chr1:9967230
|
T | A | 3 | a0001c0001t0002g0095a0001c0001t0002g0162a0001c0001t0002g0163 | 3 | HG03704.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-56-4788T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967230 | ||||||
chr1:9967231
|
C | A | 3 | a0001c0001t0002g0095a0001c0001t0002g0162a0001c0001t0002g0163 | 3 | HG03704.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-56-4787C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967231 | ||||||
chr1:9967236
|
C | CA | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-4772dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9967236 | |||||
chr1:9967244
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-56-4774A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967244 | ||||||
chr1:9967281
|
C | G | 1 | a0001c0001t0006g0285 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-56-4737C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967281 | ||||||
chr1:9967482
|
G | A | 116 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(113): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-56-4536G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967482 | ||||||
chr1:9967556
|
T | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0081 | 3 | HG02559.hp1 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-56-4462T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967556 | ||||||
chr1:9967588
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-4430A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967588 | ||||||
chr1:9967959
|
G | C | 1 | a0001c0001t0004g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-56-4059G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967959 | ||||||
chr1:9968021
|
A | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0030 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-3997A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968021 | ||||||
chr1:9968067
|
A | AGTTTTTT others(6): Show |
51 | a0001c0001t0001g0029a0001c0001t0003g0002a0001c0001t0003g0003others(48): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-56-3939_-56-3938i others(15): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968067 | |||||
chr1:9968070
|
T | TTTTTTTT others(4): Show |
6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3939_-56-3938i others(13): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968070 | |||||
chr1:9968080
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0005g0208a0001c0001t0006g0274a0001c0001t0010g0169 | 3 | HG01256.hp1 NA18983.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(12): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | |||||
chr1:9968080
|
G | GTTTTTTT others(4): Show |
97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(13): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | |||||
chr1:9968080
|
G | GTTTTTTT others(5): Show |
21 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0219others(18): Show | 21 | HG00438.hp1 HG01123.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(14): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | |||||
chr1:9968080
|
G | GTTTTTTT others(6): Show |
4 | a0001c0001t0006g0281a0001c0001t0012g0018a0001c0001t0012g0019others(1): Show | 4 | HG00558.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(15): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | |||||
chr1:9968080
|
G | T | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3938G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968080 | ||||||
chr1:9968081
|
T | TTTTTTTT others(4): Show |
2 | a0001c0001t0001g0260a0001c0001t0017g0215 | 2 | HG00741.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(13): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968081 | |||||
chr1:9968134
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-56-3884C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968134 | ||||||
chr1:9968176
|
G | A | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-56-3842G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968176 | ||||||
chr1:9968229
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3789G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968229 | ||||||
chr1:9968293
|
C | T | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3725C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968293 | ||||||
chr1:9968361
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-56-3657C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968361 | ||||||
chr1:9968362
|
G | A | 7 | a0001c0001t0006g0275a0001c0001t0006g0276a0001c0001t0006g0277others(4): Show | 7 | HG01433.hp1 HG01934.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-3656G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968362 | ||||||
chr1:9968364
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0091a0001c0001t0002g0092others(6): Show | 10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-3654G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968364 | ||||||
chr1:9968431
|
A | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(84): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56-3587A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968431 | ||||||
chr1:9968465
|
AT | A | 3 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019 | 3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-3551delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968465 | |||||
chr1:9968512
|
A | G | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3506A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968512 | ||||||
chr1:9968514
|
G | C | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-56-3504G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968514 | ||||||
chr1:9968518
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-56-3500A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968518 | ||||||
chr1:9968533
|
G | A | 1 | a0001c0001t0006g0277 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-56-3485G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968533 | ||||||
chr1:9968551
|
A | AAGGTCAG others(134): Show |
5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3457_-56-3456i others(143): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968551 | |||||
chr1:9968551
|
A | AAGGTCAG others(134): Show |
1 | a0001c0001t0013g0045 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-56-3457_-56-3456i others(143): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968551 | |||||
chr1:9968551
|
A | AAGGTCAG others(133): Show |
182 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(179): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-56-3457_-56-3456i others(142): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968551 | |||||
chr1:9968596
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3422G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968596 | ||||||
chr1:9968632
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3386G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968632 | ||||||
chr1:9968770
|
C | CA | 136 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(133): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-56-3229dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968770 | |||||
chr1:9968939
|
C | CA | 40 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0204others(37): Show | 43 | HG00438.hp2 HG00544.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-56-3062dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968939 | |||||
chr1:9968939
|
C | CAA | 6 | a0001c0001t0003g0065a0001c0001t0012g0017a0001c0001t0012g0018others(3): Show | 6 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-3063_-56-3062d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968939 | |||||
chr1:9968973
|
G | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3045G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968973 | ||||||
chr1:9969336
|
G | T | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-2682G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969336 | ||||||
chr1:9969417
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-56-2601A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969417 | ||||||
chr1:9969423
|
A | G | 5 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(2): Show | 5 | HG01109.hp1 HG01257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-2595A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969423 | ||||||
chr1:9969496
|
G | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-2522G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969496 | ||||||
chr1:9969550
|
G | A | 1 | a0001c0001t0018g0069 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-56-2468G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969550 | ||||||
chr1:9969705
|
C | G | 1 | a0001c0001t0027g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-56-2313C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969705 | ||||||
chr1:9969752
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-2266A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969752 | ||||||
chr1:9969855
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-2163A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969855 | ||||||
chr1:9969955
|
G | A | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-56-2063G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969955 | ||||||
chr1:9969974
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-2044C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969974 | ||||||
chr1:9970153
|
G | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0137 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-56-1865G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970153 | ||||||
chr1:9970249
|
A | G | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-1769A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970249 | ||||||
chr1:9970379
|
C | CTA | 9 | a0001c0001t0002g0010a0001c0001t0002g0091a0001c0001t0002g0092others(6): Show | 10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-1631_-56-1630d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9970379 | |||||
chr1:9970546
|
A | C | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-1472A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970546 | ||||||
chr1:9970572
|
C | G | 1 | a0001c0001t0002g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-56-1446C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970572 | ||||||
chr1:9970685
|
G | A | 3 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019 | 3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-1333G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970685 | ||||||
chr1:9970712
|
A | C | 1 | a0001c0001t0004g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-56-1306A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970712 | ||||||
chr1:9970899
|
A | T | 2 | a0001c0001t0015g0082a0001c0001t0015g0083 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-56-1119A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970899 | ||||||
chr1:9971030
|
TTGGGTTT others(16): Show |
T | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-987_-56-965del others(23): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971030 | ||||||
chr1:9971248
|
G | A | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-56-770G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971248 | ||||||
chr1:9971354
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-56-664G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971354 | ||||||
chr1:9971378
|
G | A | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-56-640G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971378 | ||||||
chr1:9971482
|
T | C | 2 | a0001c0001t0006g0273a0001c0001t0006g0283 | 2 | HG02074.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-56-536T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971482 | ||||||
chr1:9971572
|
A | G | 1 | a0001c0001t0004g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-56-446A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971572 | ||||||
chr1:9971973
|
G | GA | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-36dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9971973 | |||||
chr1:9972233
|
G | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+45G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972233 | ||||||
chr1:9972410
|
C | T | 1 | a0001c0001t0004g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115+222C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972410 | ||||||
chr1:9972420
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.115+232C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972420 | ||||||
chr1:9972486
|
C | T | 1 | a0001c0001t0008g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+298C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972486 | ||||||
chr1:9972494
|
C | CA | 79 | a0001c0001t0001g0029a0001c0001t0001g0193a0001c0001t0001g0225others(76): Show | 88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.115+321dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9972494 | |||||
chr1:9972494
|
C | CAA | 194 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0178others(191): Show | 206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.115+320_115+321dup others(2): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9972494 | |||||
chr1:9972494
|
C | CAAA | 8 | a0001c0001t0002g0097a0001c0001t0002g0105a0001c0001t0002g0168others(5): Show | 8 | HG02083.hp2 HG02132.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+319_115+321dup others(3): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9972494 | |||||
chr1:9972571
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.115+383A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972571 | ||||||
chr1:9972756
|
G | A | 3 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.115+568G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972756 | ||||||
chr1:9972947
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.115+759C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972947 | ||||||
chr1:9973175
|
G | C | 1 | a0001c0001t0003g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.115+987G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973175 | ||||||
chr1:9973307
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+1119G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973307 | ||||||
chr1:9973416
|
C | T | 9 | a0001c0001t0002g0010a0001c0001t0002g0091a0001c0001t0002g0092others(6): Show | 10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+1228C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973416 | ||||||
chr1:9973434
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+1246G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973434 | ||||||
chr1:9973446
|
T | G | 292 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(289): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.115+1258T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973446 | ||||||
chr1:9973707
|
C | CA | 53 | a0001c0001t0001g0182a0001c0001t0001g0202a0001c0001t0001g0219others(50): Show | 55 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.115+1544dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | |||||
chr1:9973707
|
C | CAA | 11 | a0001c0001t0002g0134a0001c0001t0004g0081a0001c0001t0004g0084others(8): Show | 11 | HG00597.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.115+1543_115+1544d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | |||||
chr1:9973707
|
CA | C | 59 | a0001c0001t0001g0198a0001c0001t0001g0225a0001c0001t0002g0009others(56): Show | 69 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.115+1544delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | |||||
chr1:9973707
|
CAAA | C | 6 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0008g0173others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+1542_115+1544d others(5): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | |||||
chr1:9973777
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+1589C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973777 | ||||||
chr1:9973868
|
C | T | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+1680C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973868 | ||||||
chr1:9973884
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.115+1696C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973884 | ||||||
chr1:9973961
|
C | G | 1 | a0001c0001t0004g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-1631C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973961 | ||||||
chr1:9973998
|
C | T | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.116-1594C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973998 | ||||||
chr1:9974217
|
A | AT | 13 | a0001c0001t0001g0266a0001c0001t0002g0130a0001c0001t0002g0161others(10): Show | 13 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-1360dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9974217 | |||||
chr1:9974327
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-1265G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974327 | ||||||
chr1:9974371
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.116-1221A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974371 | ||||||
chr1:9974390
|
A | AT | 267 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.116-1187dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9974390 | |||||
chr1:9974390
|
A | ATT | 9 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0234others(6): Show | 9 | HG00408.hp1 HG01255.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-1188_116-1187d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9974390 | |||||
chr1:9974538
|
G | A | 1 | a0001c0001t0006g0281 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.116-1054G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974538 | ||||||
chr1:9974797
|
A | T | 290 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(287): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.116-795A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974797 | ||||||
chr1:9974825
|
C | T | 2 | a0001c0001t0002g0096a0001c0001t0002g0097 | 2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.116-767C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974825 | ||||||
chr1:9974931
|
A | C | 1 | a0001c0001t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116-661A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974931 | ||||||
chr1:9974992
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116-600G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974992 | ||||||
chr1:9975023
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0224 | 2 | HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.116-569G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975023 | ||||||
chr1:9975374
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116-218G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975374 | ||||||
chr1:9975380
|
A | C | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.116-212A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975380 | ||||||
chr1:9975415
|
T | C | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.116-177T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975415 | ||||||
chr1:9975450
|
G | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0049 | 2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.116-142G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975450 | ||||||
chr1:9975859
|
A | G | 3 | a0001c0001t0004g0143a0001c0001t0004g0153a0001c0001t0004g0154 | 3 | HG03139.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.299+84A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9975859 | ||||||
chr1:9975951
|
G | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(53): Show | 64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.299+176G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9975951 | ||||||
chr1:9976156
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+381G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976156 | ||||||
chr1:9976274
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+499G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976274 | ||||||
chr1:9976286
|
C | CA | 8 | a0001c0001t0001g0178a0001c0001t0001g0229a0001c0001t0001g0267others(5): Show | 8 | HG00280.hp2 HG01433.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.299+530dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9976286 | |||||
chr1:9976286
|
CA | C | 13 | a0001c0001t0001g0192a0001c0001t0002g0074a0001c0001t0002g0112others(10): Show | 13 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.299+530delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9976286 | |||||
chr1:9976307
|
A | T | 1 | a0001c0001t0004g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299+532A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976307 | ||||||
chr1:9976469
|
A | T | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+694A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976469 | ||||||
chr1:9976470
|
G | A | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+695G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976470 | ||||||
chr1:9976471
|
C | A | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+696C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976471 | ||||||
chr1:9976472
|
A | T | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+697A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976472 | ||||||
chr1:9976474
|
C | T | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+699C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976474 | ||||||
chr1:9976475
|
C | A | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+700C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976475 | ||||||
chr1:9976477
|
GTGCT | G | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+703_299+706del others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976477 | ||||||
chr1:9976484
|
T | C | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+709T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976484 | ||||||
chr1:9976487
|
A | T | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+712A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976487 | ||||||
chr1:9976488
|
T | C | 13 | a0001c0001t0002g0124a0001c0001t0005g0246a0001c0001t0005g0247others(10): Show | 13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+713T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976488 | ||||||
chr1:9976681
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299+906G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976681 | ||||||
chr1:9976889
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299+1114C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976889 | ||||||
chr1:9976912
|
C | CT | 64 | a0001c0001t0001g0202a0001c0001t0001g0266a0001c0001t0003g0002others(61): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.299+1148dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9976912 | |||||
chr1:9976929
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.299+1154A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976929 | ||||||
chr1:9977033
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.299+1258A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977033 | ||||||
chr1:9977068
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+1293G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977068 | ||||||
chr1:9977148
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.299+1373C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977148 | ||||||
chr1:9977161
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299+1386G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977161 | ||||||
chr1:9977178
|
G | C | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+1403G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977178 | ||||||
chr1:9977227
|
A | C | 1 | a0001c0001t0001g0194 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.299+1452A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977227 | ||||||
chr1:9977399
|
T | C | 3 | a0001c0001t0002g0074a0001c0001t0002g0106a0001c0001t0002g0125 | 3 | NA18990.hp2 NA19001.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.299+1624T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977399 | ||||||
chr1:9977410
|
A | T | 116 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.299+1635A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977410 | ||||||
chr1:9977588
|
C | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0195 | 2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.299+1813C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977588 | ||||||
chr1:9977589
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.299+1814G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977589 | ||||||
chr1:9977621
|
C | T | 1 | a0001c0001t0019g0291 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299+1846C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977621 | ||||||
chr1:9977640
|
G | A | 2 | a0001c0001t0007g0075a0001c0001t0007g0077 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.299+1865G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977640 | ||||||
chr1:9977868
|
C | A | 1 | a0001c0001t0002g0139 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.299+2093C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977868 | ||||||
chr1:9978081
|
G | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+2306G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978081 | ||||||
chr1:9978312
|
C | T | 1 | a0001c0001t0027g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299+2537C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978312 | ||||||
chr1:9978341
|
G | A | 1 | a0001c0001t0018g0069 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.299+2566G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978341 | ||||||
chr1:9978351
|
G | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+2576G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978351 | ||||||
chr1:9978360
|
A | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0032others(13): Show | 21 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.299+2585A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978360 | ||||||
chr1:9978373
|
G | A | 1 | a0001c0001t0001g0194 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.299+2598G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978373 | ||||||
chr1:9978379
|
C | T | 2 | a0001c0001t0014g0016a0001c0001t0014g0020 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.299+2604C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978379 | ||||||
chr1:9978427
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.300-2604T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978427 | ||||||
chr1:9978459
|
G | A | 1 | a0003c0003t0021g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.300-2572G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978459 | ||||||
chr1:9978597
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.300-2434C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978597 | ||||||
chr1:9978629
|
G | A | 1 | a0001c0001t0005g0258 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.300-2402G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978629 | ||||||
chr1:9978659
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.300-2372C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978659 | ||||||
chr1:9978870
|
C | T | 2 | a0001c0001t0004g0084a0001c0001t0004g0089 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.300-2161C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978870 | ||||||
chr1:9978947
|
C | T | 1 | a0001c0001t0016g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.300-2084C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978947 | ||||||
chr1:9979061
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.300-1970G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979061 | ||||||
chr1:9979089
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.300-1942T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979089 | ||||||
chr1:9979161
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.300-1870C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979161 | ||||||
chr1:9979304
|
C | A | 280 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.300-1727C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979304 | ||||||
chr1:9979533
|
G | T | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.300-1498G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979533 | ||||||
chr1:9979627
|
T | C | 2 | a0001c0001t0004g0144a0001c0001t0004g0152 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.300-1404T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979627 | ||||||
chr1:9979760
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.300-1271C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979760 | ||||||
chr1:9979801
|
C | CA | 15 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0212others(12): Show | 15 | HG00639.hp2 HG01255.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.300-1213dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9979801 | |||||
chr1:9979801
|
CA | C | 7 | a0001c0001t0002g0097a0001c0001t0008g0031a0001c0001t0008g0173others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.300-1213delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9979801 | |||||
chr1:9979933
|
AT | A | 32 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0179others(29): Show | 33 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.300-1088delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9979933 | |||||
chr1:9980152
|
G | A | 5 | a0001c0001t0010g0021a0001c0001t0010g0169a0001c0001t0010g0170others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.300-879G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980152 | ||||||
chr1:9980191
|
C | T | 1 | a0001c0001t0005g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.300-840C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980191 | ||||||
chr1:9980372
|
A | T | 1 | a0001c0001t0003g0023 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.300-659A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980372 | ||||||
chr1:9980451
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.300-580A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980451 | ||||||
chr1:9980464
|
CA | C | 277 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.300-558delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9980464 | |||||
chr1:9980494
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.300-537G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980494 | ||||||
chr1:9980683
|
G | C | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-348G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980683 | ||||||
chr1:9980710
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.300-321G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980710 | ||||||
chr1:9980728
|
C | T | 1 | a0001c0001t0018g0069 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.300-303C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980728 | ||||||
chr1:9981195
|
C | T | 2 | a0001c0001t0004g0084a0001c0001t0004g0089 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.439+25C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981195 | ||||||
chr1:9981238
|
G | C | 1 | a0001c0001t0004g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.439+68G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981238 | ||||||
chr1:9981393
|
C | A | 5 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(2): Show | 5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+223C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981393 | ||||||
chr1:9981527
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+357G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981527 | ||||||
chr1:9981598
|
T | C | 1 | a0001c0001t0005g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.439+428T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981598 | ||||||
chr1:9981695
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.439+525C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981695 | ||||||
chr1:9981762
|
G | A | 1 | a0001c0001t0006g0289 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.440-539G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981762 | ||||||
chr1:9981908
|
G | T | 6 | a0001c0001t0008g0031a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-393G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981908 | ||||||
chr1:9981919
|
G | A | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0029others(117): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.440-382G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981919 | ||||||
chr1:9981956
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.440-345C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981956 | ||||||
chr1:9982006
|
G | C | 1 | a0001c0001t0020g0026 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.440-295G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9982006 | ||||||
chr1:9982075
|
C | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(53): Show | 64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.440-226C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9982075 |