geneid | 27020 |
---|---|
ensemblid | ENSG00000156642.17 |
hgncid | 17867 |
symbol | NPTN |
name | neuroplastin |
refseq_nuc | NM_012428.4 |
refseq_prot | NP_036560.1 |
ensembl_nuc | ENST00000345330.9 |
ensembl_prot | ENSP00000290401.4 |
mane_status | MANE Select |
chr | chr15 |
start | 73560014 |
end | 73633389 |
strand | - |
ver | v1.2 |
region | chr15:73560014-73633389 |
region5000 | chr15:73555014-73638389 |
regionname0 | NPTN_chr15_73560014_73633389 |
regionname5000 | NPTN_chr15_73555014_73638389 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 398 | 342 | 78 | 58 | 162 | 8 | 34 | 132 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1224 | 321 | 76 | 57 | 146 | 6 | 34 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
t0002 | 0/0 | 1224 | 15 | 0 | 0 | 13 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
t0003 | 0/0 | 1224 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
t0004 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
t0005 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
t0006 | 0/0 | 1224 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1197 | 340 | 76 | 58 | 162 | 8 | 34 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0002 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2420 | 319 | 74 | 57 | 146 | 6 | 34 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0001t0002 | 0/0 | 2420 | 15 | 0 | 0 | 13 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0001t0003 | 0/0 | 2420 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0001t0004 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0001t0005 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0001t0006 | 0/0 | 2420 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
a0001c0002t0001 | 0/0 | 2420 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | copy fasta | chr15 | 73555014 | 73638389 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0289 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CDX | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0257 | REF | REF | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0151 | REF | REF | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73570265
|
C | T | 1 | a0001c0002 | 2 | HG02280.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.999G>A | p.Val333Val | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/9 | 1173/2420 | 999/1197 | 333/398 | chr15 | 73570265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73560123
|
C | T | 1 | a0001c0001t0005 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 9/9 | 1787 | chr15 | 73560123 | |||||
chr15:73560367
|
A | G | 1 | a0001c0001t0004 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 9/9 | 1543 | chr15 | 73560367 | |||||
chr15:73560948
|
G | A | 1 | a0001c0001t0002 | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*115C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 9/9 | 962 | chr15 | 73560948 | |||||
chr15:73633294
|
G | C | 1 | a0001c0001t0006 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/9 | 79 | chr15 | 73633294 | |||||
chr15:73633354
|
C | T | 1 | a0001c0001t0003 | 3 | NA18965.hp2 NA18994.hp1 NA19002.hp2 |
5_prime_UTR_variant | MODIFIER | c.-139G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/9 | 139 | chr15 | 73633354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73561145
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.*15-97C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561145 | ||||||
chr15:73561409
|
T | C | 1 | a0001c0001t0002g0227 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.*15-361A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561409 | ||||||
chr15:73561454
|
C | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.*15-406G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561454 | ||||||
chr15:73561455
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.*15-407C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561455 | ||||||
chr15:73561468
|
T | C | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.*15-420A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561468 | ||||||
chr15:73561661
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.*14+235A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561661 | ||||||
chr15:73561740
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*14+156T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561740 | ||||||
chr15:73562191
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1137-221A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562191 | ||||||
chr15:73562249
|
A | C | 1 | a0001c0001t0001g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1137-279T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562249 | ||||||
chr15:73562268
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1137-298G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562268 | ||||||
chr15:73562610
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1136+626A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562610 | ||||||
chr15:73562657
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 18 | HG01496.hp2 HG02055.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136+579C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562657 | ||||||
chr15:73562702
|
T | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0030others(75): Show | 94 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+534A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562702 | ||||||
chr15:73562896
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1136+340C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562896 | ||||||
chr15:73562989
|
G | GA | 33 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 38 | HG00558.hp1 HG00639.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1136+246dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562989 | ||||||
chr15:73563014
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1136+222C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73563014 | ||||||
chr15:73563173
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1136+63T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73563173 | ||||||
chr15:73563297
|
A | G | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1115-40T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563297 | ||||||
chr15:73563706
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1115-449G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563706 | ||||||
chr15:73563735
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1115-478T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563735 | ||||||
chr15:73563748
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1115-491A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563748 | ||||||
chr15:73563844
|
A | G | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1115-587T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563844 | ||||||
chr15:73563962
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1115-705G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563962 | ||||||
chr15:73564104
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1115-847T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564104 | ||||||
chr15:73564501
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1115-1244G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564501 | ||||||
chr15:73564529
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1115-1272A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564529 | ||||||
chr15:73564658
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-1401T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564658 | ||||||
chr15:73564707
|
C | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143others(14): Show | 24 | HG01346.hp1 HG01516.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1115-1450G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564707 | ||||||
chr15:73564739
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1115-1482G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564739 | ||||||
chr15:73564995
|
A | T | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 34 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1115-1738T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564995 | ||||||
chr15:73565065
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1115-1808C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565065 | ||||||
chr15:73565250
|
C | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1115-1993G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565250 | ||||||
chr15:73565822
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115-2565C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565822 | ||||||
chr15:73565885
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143others(14): Show | 24 | HG01346.hp1 HG01516.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1115-2628A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565885 | ||||||
chr15:73565899
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1115-2642G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565899 | ||||||
chr15:73566074
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 122 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1115-2817T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566074 | ||||||
chr15:73566279
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1115-3022C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566279 | ||||||
chr15:73566296
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0285 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1115-3039A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566296 | ||||||
chr15:73566506
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0287a0001c0001t0001g0288 | 4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-3249A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566506 | ||||||
chr15:73566524
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115-3267T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566524 | ||||||
chr15:73566675
|
A | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(88): Show | 108 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1115-3418T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566675 | ||||||
chr15:73566786
|
G | C | 1 | a0001c0001t0001g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1114+3364C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566786 | ||||||
chr15:73566842
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1114+3308C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566842 | ||||||
chr15:73566967
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+3183C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566967 | ||||||
chr15:73567001
|
GCTTTT | G | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+3144_1114+314 others(9): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567001 | ||||||
chr15:73567002
|
C | CT | 5 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0238others(2): Show | 8 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114+3147dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | ||||||
chr15:73567002
|
CT | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 228 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.1114+3147delA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | ||||||
chr15:73567002
|
CTT | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0094others(7): Show | 10 | HG00642.hp1 HG01069.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114+3146_1114+314 others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | ||||||
chr15:73567002
|
CTTTT | C | 45 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(42): Show | 51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1114+3144_1114+314 others(8): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | ||||||
chr15:73567128
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1114+3022A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567128 | ||||||
chr15:73567147
|
T | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 121 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1114+3003A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567147 | ||||||
chr15:73567166
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1114+2984A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567166 | ||||||
chr15:73567221
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+2929A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567221 | ||||||
chr15:73567234
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+2916T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567234 | ||||||
chr15:73567315
|
G | T | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1114+2835C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567315 | ||||||
chr15:73567514
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 218 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(215): Show |
intron_variant | MODIFIER | c.1114+2636C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567514 | ||||||
chr15:73567531
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1114+2619A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567531 | ||||||
chr15:73567628
|
CT | C | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+2521delA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567628 | ||||||
chr15:73567813
|
G | A | 1 | a0001c0001t0001g0012 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1114+2337C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567813 | ||||||
chr15:73567902
|
C | T | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1114+2248G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567902 | ||||||
chr15:73567952
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114+2198C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567952 | ||||||
chr15:73567977
|
A | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(58): Show | 70 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1114+2173T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567977 | ||||||
chr15:73568019
|
C | T | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1114+2131G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568019 | ||||||
chr15:73568141
|
T | TG | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+2008dupC | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568141 | ||||||
chr15:73568148
|
A | G | 50 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(47): Show | 56 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1114+2002T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568148 | ||||||
chr15:73568162
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1114+1988A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568162 | ||||||
chr15:73568163
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1114+1987G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568163 | ||||||
chr15:73568194
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0287a0001c0001t0001g0288 | 4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+1956A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568194 | ||||||
chr15:73568206
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1114+1944C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568206 | ||||||
chr15:73568306
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1114+1844G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568306 | ||||||
chr15:73568699
|
G | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0258a0001c0001t0001g0260others(4): Show | 8 | HG02015.hp2 HG02083.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+1451C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568699 | ||||||
chr15:73569032
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1114+1118A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569032 | ||||||
chr15:73569103
|
C | T | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114+1047G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569103 | ||||||
chr15:73569180
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+970G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569180 | ||||||
chr15:73569217
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1114+933C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569217 | ||||||
chr15:73569299
|
C | G | 1 | a0001c0002t0001g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114+851G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569299 | ||||||
chr15:73569300
|
G | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0259others(1): Show | 6 | NA18969.hp1 NA18984.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+850C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569300 | ||||||
chr15:73569562
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1114+588G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569562 | ||||||
chr15:73569571
|
A | C | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1114+579T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569571 | ||||||
chr15:73569911
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1114+239T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569911 | ||||||
chr15:73569964
|
TAAAATA | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+180_1114+185d others(8): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569964 | ||||||
chr15:73569995
|
C | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 81 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.1114+155G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569995 | ||||||
chr15:73570426
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.841-3C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570426 | ||||||
chr15:73570729
|
TAAGAAAC others(6): Show |
T | 1 | a0001c0001t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.841-319_841-307del others(13): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570729 | ||||||
chr15:73570773
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.841-350G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570773 | ||||||
chr15:73570861
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.841-438C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570861 | ||||||
chr15:73571285
|
G | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 281 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(278): Show |
intron_variant | MODIFIER | c.841-862C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571285 | ||||||
chr15:73571416
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.841-993G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571416 | ||||||
chr15:73571584
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-1161T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571584 | ||||||
chr15:73571659
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.841-1236C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571659 | ||||||
chr15:73572334
|
C | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.840+1328G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572334 | ||||||
chr15:73572335
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0020others(98): Show | 116 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.840+1327C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572335 | ||||||
chr15:73572490
|
C | T | 35 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 41 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.840+1172G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572490 | ||||||
chr15:73572522
|
CCCTTGGG others(73): Show |
C | 2 | a0001c0001t0001g0005a0001c0001t0001g0066 | 4 | NA18960.hp2 NA19007.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1060_840+1139d others(82): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572522 | ||||||
chr15:73572800
|
G | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 7 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+862C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572800 | ||||||
chr15:73572862
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+800C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572862 | ||||||
chr15:73572867
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.840+795T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572867 | ||||||
chr15:73573228
|
C | T | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.840+434G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573228 | ||||||
chr15:73573326
|
TA | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+335delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573326 | ||||||
chr15:73573455
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.840+207C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573455 | ||||||
chr15:73573623
|
A | T | 1 | a0001c0001t0003g0036 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.840+39T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573623 | ||||||
chr15:73573882
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.707-87A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73573882 | ||||||
chr15:73574015
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.707-220C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574015 | ||||||
chr15:73574039
|
A | C | 1 | a0001c0001t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.707-244T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574039 | ||||||
chr15:73574671
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-876G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574671 | ||||||
chr15:73574693
|
G | A | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG02155.hp2 HG04184.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.707-898C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574693 | ||||||
chr15:73574883
|
T | G | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.707-1088A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574883 | ||||||
chr15:73575499
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-1704A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575499 | ||||||
chr15:73575534
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.707-1739G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575534 | ||||||
chr15:73575544
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.707-1749C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575544 | ||||||
chr15:73575685
|
C | G | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.707-1890G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575685 | ||||||
chr15:73575717
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18974.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.707-1922A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575717 | ||||||
chr15:73575755
|
T | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0221 | 2 | HG02015.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.707-1960A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575755 | ||||||
chr15:73575995
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-2200G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575995 | ||||||
chr15:73576002
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.707-2207C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576002 | ||||||
chr15:73576355
|
GTCTC | G | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.707-2564_707-2561d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576355 | ||||||
chr15:73576395
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.707-2600G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576395 | ||||||
chr15:73576475
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.707-2680A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576475 | ||||||
chr15:73576621
|
G | A | 8 | a0001c0001t0001g0047a0001c0001t0001g0207a0001c0001t0001g0209others(5): Show | 8 | HG01261.hp2 HG01975.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.707-2826C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576621 | ||||||
chr15:73576768
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.707-2973G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576768 | ||||||
chr15:73576950
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.707-3155C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576950 | ||||||
chr15:73577213
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.707-3418C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577213 | ||||||
chr15:73577234
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-3439G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577234 | ||||||
chr15:73577426
|
G | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 165 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.707-3631C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577426 | ||||||
chr15:73577567
|
T | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 215 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.707-3772A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577567 | ||||||
chr15:73577621
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.707-3826T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577621 | ||||||
chr15:73577818
|
G | A | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 34 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.707-4023C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577818 | ||||||
chr15:73577831
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-4036C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577831 | ||||||
chr15:73577951
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.707-4156A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577951 | ||||||
chr15:73577953
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0070 | 5 | NA18960.hp2 NA18986.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-4158A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577953 | ||||||
chr15:73577961
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.707-4166G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577961 | ||||||
chr15:73578020
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.707-4225G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578020 | ||||||
chr15:73578105
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0145 | 3 | NA18952.hp1 NA18986.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.707-4310G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578105 | ||||||
chr15:73578212
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.707-4417G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578212 | ||||||
chr15:73578229
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.707-4434T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578229 | ||||||
chr15:73578456
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-4661A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578456 | ||||||
chr15:73578460
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.707-4665A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578460 | ||||||
chr15:73578681
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-4886G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578681 | ||||||
chr15:73578701
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.707-4906C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578701 | ||||||
chr15:73578718
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.707-4923C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578718 | ||||||
chr15:73578899
|
G | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.707-5104C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578899 | ||||||
chr15:73578992
|
C | CA | 34 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(31): Show | 38 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.707-5198dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578992 | ||||||
chr15:73578992
|
C | CAA | 5 | a0001c0001t0001g0035a0001c0001t0001g0254a0001c0001t0001g0280others(2): Show | 6 | HG01243.hp2 HG01255.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-5199_707-5198d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578992 | ||||||
chr15:73578992
|
CA | C | 12 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0075others(9): Show | 12 | HG01109.hp1 HG01169.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.707-5198delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578992 | ||||||
chr15:73579144
|
T | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.707-5349A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579144 | ||||||
chr15:73579171
|
C | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0106others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.707-5376G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579171 | ||||||
chr15:73579172
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0197 | 2 | HG01081.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.707-5377C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579172 | ||||||
chr15:73579233
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.707-5438G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579233 | ||||||
chr15:73579277
|
CA | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 188 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.707-5483delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579277 | ||||||
chr15:73579441
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.707-5646T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579441 | ||||||
chr15:73579500
|
G | T | 1 | a0001c0001t0001g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.707-5705C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579500 | ||||||
chr15:73579660
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.707-5865C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579660 | ||||||
chr15:73579999
|
T | C | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.707-6204A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579999 | ||||||
chr15:73580158
|
C | T | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.707-6363G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580158 | ||||||
chr15:73580181
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.707-6386C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580181 | ||||||
chr15:73580230
|
G | A | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.707-6435C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580230 | ||||||
chr15:73580271
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.707-6476C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580271 | ||||||
chr15:73580400
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0001g0186 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.707-6627_707-6606d others(24): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | ||||||
chr15:73580400
|
TTATATAT others(4): Show |
T | 33 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 39 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.707-6616_707-6606d others(13): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | ||||||
chr15:73580400
|
TTATATAT others(15): Show |
T | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.707-6627_707-6606d others(24): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | ||||||
chr15:73580400
|
TTATATAT others(28): Show |
T | 1 | a0001c0002t0001g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.707-6640_707-6606d others(37): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | ||||||
chr15:73580401
|
T | TATATATA others(24): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0145 | 3 | NA18952.hp1 NA18986.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.707-6637_707-6607d others(33): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580401 | ||||||
chr15:73580410
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.707-6615T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580410 | ||||||
chr15:73580411
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.707-6634_707-6617d others(20): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580411 | ||||||
chr15:73580411
|
A | ATATATAT others(283): Show |
1 | a0001c0002t0001g0283 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.707-6617_707-6616i others(292): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580411 | ||||||
chr15:73580411
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.707-6616T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580411 | ||||||
chr15:73580412
|
TATATATA others(22): Show |
T | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.707-6646_707-6618d others(31): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580412 | ||||||
chr15:73580419
|
ATAATATA others(3): Show |
A | 1 | a0001c0001t0001g0265 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.707-6634_707-6625d others(12): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580419 | ||||||
chr15:73580421
|
A | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.707-6626T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580421 | ||||||
chr15:73580422
|
A | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.707-6627T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580422 | ||||||
chr15:73580430
|
ATAATATA others(1): Show |
A | 3 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0133 | 5 | HG00733.hp2 HG00735.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-6643_707-6636d others(10): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580430 | ||||||
chr15:73580432
|
A | T | 1 | a0001c0001t0001g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.707-6637T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580432 | ||||||
chr15:73580433
|
A | T | 1 | a0001c0001t0001g0265 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.707-6638T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580433 | ||||||
chr15:73580440
|
TA | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0133 | 5 | HG00733.hp2 HG00735.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-6646delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580440 | ||||||
chr15:73580441
|
A | AAT | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(112): Show | 138 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.707-6648_707-6647d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580441 | ||||||
chr15:73580441
|
A | ATAATATA others(13): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-6647_707-6646i others(22): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580441 | ||||||
chr15:73580441
|
A | T | 49 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 55 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.707-6646T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580441 | ||||||
chr15:73580442
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0236others(4): Show | 10 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.707-6647T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580442 | ||||||
chr15:73580450
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0236others(4): Show | 10 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.707-6655C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580450 | ||||||
chr15:73580451
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.707-6656A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580451 | ||||||
chr15:73580451
|
T | TA | 7 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0236others(4): Show | 10 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.707-6657dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580451 | ||||||
chr15:73580459
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6664G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580459 | ||||||
chr15:73580460
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6665T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580460 | ||||||
chr15:73580462
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6667T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580462 | ||||||
chr15:73580469
|
T | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6674A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580469 | ||||||
chr15:73580469
|
TTATATAT others(9): Show |
T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.707-6690_707-6675d others(18): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580469 | ||||||
chr15:73580478
|
C | CAAA | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6684_707-6683i others(5): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580478 | ||||||
chr15:73580482
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6687T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580482 | ||||||
chr15:73580482
|
AAT | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(2): Show | 5 | HG02559.hp1 HG02970.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-6689_707-6688d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580482 | ||||||
chr15:73580485
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(5): Show | 11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6690T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580485 | ||||||
chr15:73580498
|
AATAT | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0145a0001c0001t0003g0036others(2): Show | 6 | NA18952.hp1 NA18965.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-6707_707-6704d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580498 | ||||||
chr15:73580516
|
A | AAT | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.707-6723_707-6722d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580516 | ||||||
chr15:73580516
|
AAT | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 17 | HG01496.hp2 HG02055.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.707-6723_707-6722d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580516 | ||||||
chr15:73580523
|
TTATATAT others(20): Show |
T | 3 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0065 | 4 | NA18942.hp2 NA18952.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.707-6755_707-6729d others(29): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580523 | ||||||
chr15:73580569
|
TTATATAT others(20): Show |
T | 23 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(20): Show | 23 | HG00438.hp1 HG00735.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.707-6801_707-6775d others(29): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580569 | ||||||
chr15:73580572
|
T | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 7 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.707-6777A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580572 | ||||||
chr15:73580588
|
TTATATAT others(1): Show |
T | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-6801_707-6794d others(10): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580588 | ||||||
chr15:73580623
|
G | GTATATAT others(12): Show |
1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.707-6847_707-6829d others(21): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580623 | ||||||
chr15:73580656
|
ATT | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0192 | 4 | HG00597.hp1 HG02071.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-6863_707-6862d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580656 | ||||||
chr15:73580664
|
C | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 122 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.706+6860G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580664 | ||||||
chr15:73580721
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.706+6803A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580721 | ||||||
chr15:73580798
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.706+6726A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580798 | ||||||
chr15:73580828
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.706+6696C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580828 | ||||||
chr15:73580933
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0111 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.706+6591A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580933 | ||||||
chr15:73580952
|
C | CT | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+6571dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580952 | ||||||
chr15:73581067
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01361.hp1 HG01928.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.706+6457C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581067 | ||||||
chr15:73581124
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.706+6400G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581124 | ||||||
chr15:73581502
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.706+6022G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581502 | ||||||
chr15:73581540
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(2): Show | 5 | HG01943.hp2 HG01981.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.706+5984G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581540 | ||||||
chr15:73581605
|
C | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 10 | HG00621.hp2 HG02132.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+5919G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581605 | ||||||
chr15:73581673
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.706+5851A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581673 | ||||||
chr15:73581703
|
C | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.706+5821G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581703 | ||||||
chr15:73581757
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.706+5767A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581757 | ||||||
chr15:73581826
|
A | T | 1 | a0001c0001t0001g0265 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.706+5698T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581826 | ||||||
chr15:73581836
|
C | CT | 6 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0265others(3): Show | 8 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.706+5687dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581836 | ||||||
chr15:73581848
|
C | T | 49 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 55 | HG00438.hp1 HG00558.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.706+5676G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581848 | ||||||
chr15:73581971
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.706+5553T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581971 | ||||||
chr15:73582020
|
G | C | 1 | a0001c0001t0001g0035 | 2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.706+5504C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582020 | ||||||
chr15:73582307
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.706+5217A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582307 | ||||||
chr15:73582400
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.706+5124C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582400 | ||||||
chr15:73582573
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.706+4951G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582573 | ||||||
chr15:73582591
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+4933G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582591 | ||||||
chr15:73582868
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+4656G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582868 | ||||||
chr15:73582888
|
T | C | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.706+4636A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582888 | ||||||
chr15:73582946
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.706+4578G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582946 | ||||||
chr15:73583272
|
G | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.706+4252C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583272 | ||||||
chr15:73583326
|
C | T | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.706+4198G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583326 | ||||||
chr15:73583385
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.706+4139G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583385 | ||||||
chr15:73583487
|
G | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+4037C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583487 | ||||||
chr15:73583881
|
G | A | 50 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(47): Show | 56 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.706+3643C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583881 | ||||||
chr15:73584068
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.706+3456G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584068 | ||||||
chr15:73584081
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.706+3443G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584081 | ||||||
chr15:73584290
|
T | G | 3 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038 | 3 | NA18965.hp2 NA18994.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.706+3234A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584290 | ||||||
chr15:73584660
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 107 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.706+2864G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584660 | ||||||
chr15:73584702
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.706+2822A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584702 | ||||||
chr15:73584764
|
T | TA | 38 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0031others(35): Show | 45 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.706+2759dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584764 | ||||||
chr15:73584764
|
TA | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0090a0001c0001t0001g0100others(7): Show | 10 | HG01069.hp2 HG01169.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+2759delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584764 | ||||||
chr15:73584765
|
A | T | 6 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | NA18969.hp2 NA18975.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.706+2759T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584765 | ||||||
chr15:73584806
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.706+2718G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584806 | ||||||
chr15:73584963
|
T | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 5 | HG02293.hp2 NA18974.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.706+2561A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584963 | ||||||
chr15:73585039
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.706+2485G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585039 | ||||||
chr15:73585149
|
T | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.706+2375A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585149 | ||||||
chr15:73585149
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.706+2375A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585149 | ||||||
chr15:73585419
|
A | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+2105T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585419 | ||||||
chr15:73585435
|
G | A | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.706+2089C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585435 | ||||||
chr15:73585678
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(99): Show | 120 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.706+1846T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585678 | ||||||
chr15:73585768
|
C | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0092 | 2 | HG00544.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.706+1756G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585768 | ||||||
chr15:73585886
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0153 | 2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.706+1638C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585886 | ||||||
chr15:73585888
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.706+1636C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585888 | ||||||
chr15:73585934
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.706+1590T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585934 | ||||||
chr15:73585969
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+1555G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585969 | ||||||
chr15:73585986
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.706+1538C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585986 | ||||||
chr15:73586203
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.706+1321C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586203 | ||||||
chr15:73586229
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 218 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(215): Show |
intron_variant | MODIFIER | c.706+1295T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586229 | ||||||
chr15:73586491
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.706+1033T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586491 | ||||||
chr15:73586802
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.706+722A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586802 | ||||||
chr15:73587151
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.706+373G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587151 | ||||||
chr15:73587155
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.706+369C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587155 | ||||||
chr15:73587251
|
C | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 10 | HG00621.hp2 HG02132.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+273G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587251 | ||||||
chr15:73587299
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.706+225C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587299 | ||||||
chr15:73587692
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-74C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587692 | ||||||
chr15:73587729
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.612-111G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587729 | ||||||
chr15:73587752
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.612-134T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587752 | ||||||
chr15:73587926
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 5 | HG02293.hp2 NA18974.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-308C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587926 | ||||||
chr15:73587977
|
C | G | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-359G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587977 | ||||||
chr15:73587982
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.612-364G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587982 | ||||||
chr15:73588414
|
G | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG02523.hp2 NA18998.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.612-796C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588414 | ||||||
chr15:73588439
|
G | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.612-821C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588439 | ||||||
chr15:73588502
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-884G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588502 | ||||||
chr15:73588503
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-885T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588503 | ||||||
chr15:73588506
|
G | C | 1 | a0001c0001t0001g0270 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-888C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588506 | ||||||
chr15:73588986
|
A | T | 1 | a0001c0001t0001g0019 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.612-1368T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588986 | ||||||
chr15:73589083
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-1465C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589083 | ||||||
chr15:73589254
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.612-1636G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589254 | ||||||
chr15:73589396
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 5 | HG02293.hp2 NA18974.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-1778G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589396 | ||||||
chr15:73589427
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-1809G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589427 | ||||||
chr15:73589504
|
A | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143 | 5 | HG02145.hp1 HG02622.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-1886T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589504 | ||||||
chr15:73589592
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.612-1974C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589592 | ||||||
chr15:73589715
|
G | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-2097C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589715 | ||||||
chr15:73589753
|
T | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 5 | NA18949.hp2 NA18961.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-2135A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589753 | ||||||
chr15:73589817
|
C | CAA | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 330 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(327): Show |
intron_variant | MODIFIER | c.611+2148_611+2149i others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589817 | ||||||
chr15:73590126
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.611+1840A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590126 | ||||||
chr15:73590416
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611+1550T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590416 | ||||||
chr15:73590607
|
C | CA | 69 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0031others(66): Show | 81 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.611+1358dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590607 | ||||||
chr15:73590884
|
T | A | 1 | a0001c0001t0001g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.611+1082A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590884 | ||||||
chr15:73590884
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.611+1082A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590884 | ||||||
chr15:73590923
|
G | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.611+1043C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590923 | ||||||
chr15:73591198
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.611+768C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591198 | ||||||
chr15:73591519
|
C | T | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+447G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591519 | ||||||
chr15:73591582
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+384A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591582 | ||||||
chr15:73591751
|
A | G | 6 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159others(3): Show | 6 | HG01943.hp2 HG01952.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.611+215T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591751 | ||||||
chr15:73591826
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+140C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591826 | ||||||
chr15:73591941
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.611+25G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591941 | ||||||
chr15:73592184
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.440-47G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592184 | ||||||
chr15:73592367
|
C | T | 45 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(42): Show | 51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.440-230G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592367 | ||||||
chr15:73592447
|
C | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0212 | 2 | HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.440-310G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592447 | ||||||
chr15:73592470
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.440-333A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592470 | ||||||
chr15:73592560
|
C | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0145a0001c0001t0003g0036others(2): Show | 6 | NA18952.hp1 NA18965.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-423G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592560 | ||||||
chr15:73592625
|
G | A | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(4): Show | 7 | HG00438.hp1 HG02155.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-488C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592625 | ||||||
chr15:73592627
|
C | A | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440-490G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592627 | ||||||
chr15:73592806
|
C | T | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.440-669G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592806 | ||||||
chr15:73593062
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0006g0289 | 2 | HG01346.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.440-925C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593062 | ||||||
chr15:73593102
|
G | A | 45 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(42): Show | 51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.440-965C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593102 | ||||||
chr15:73593198
|
T | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 122 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.440-1061A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593198 | ||||||
chr15:73593303
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 7 | HG01346.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-1166T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593303 | ||||||
chr15:73593504
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 7 | HG01346.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-1367G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593504 | ||||||
chr15:73593927
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.440-1790C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593927 | ||||||
chr15:73593956
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.440-1819C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593956 | ||||||
chr15:73594085
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.440-1948T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594085 | ||||||
chr15:73594508
|
G | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 107 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.440-2371C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594508 | ||||||
chr15:73594534
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.440-2397G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594534 | ||||||
chr15:73594871
|
C | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG00673.hp2 NA18955.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2151G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594871 | ||||||
chr15:73594951
|
T | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0167others(1): Show | 4 | HG00544.hp1 NA18949.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2071A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594951 | ||||||
chr15:73594951
|
T | TA | 34 | a0001c0001t0001g0007a0001c0001t0001g0122a0001c0001t0001g0132others(31): Show | 39 | HG00438.hp1 HG01109.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.439+2070dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594951 | ||||||
chr15:73594951
|
TA | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG02559.hp1 HG02897.hp2 NA18522.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+2070delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594951 | ||||||
chr15:73595005
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.439+2017T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595005 | ||||||
chr15:73595116
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.439+1906A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595116 | ||||||
chr15:73595143
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+1879G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595143 | ||||||
chr15:73595345
|
T | TA | 13 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0122others(10): Show | 14 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.439+1676dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595345 | ||||||
chr15:73595384
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.439+1638T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595384 | ||||||
chr15:73595564
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.439+1458C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595564 | ||||||
chr15:73595642
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.439+1380T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595642 | ||||||
chr15:73595750
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.439+1272G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595750 | ||||||
chr15:73595824
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.439+1198A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595824 | ||||||
chr15:73595838
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.439+1184A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595838 | ||||||
chr15:73595890
|
CAT | C | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.439+1130_439+1131d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595890 | ||||||
chr15:73595896
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 5 | NA18962.hp1 NA18968.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+1126A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595896 | ||||||
chr15:73595981
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.439+1041C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595981 | ||||||
chr15:73596574
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.439+448G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73596574 | ||||||
chr15:73596748
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+274C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73596748 | ||||||
chr15:73597386
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.92-17G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597386 | ||||||
chr15:73597411
|
G | GA | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-43dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597411 | ||||||
chr15:73597690
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92-321G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597690 | ||||||
chr15:73597785
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.92-416A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597785 | ||||||
chr15:73597829
|
C | T | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-460G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597829 | ||||||
chr15:73598041
|
C | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(51): Show | 63 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.92-672G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598041 | ||||||
chr15:73598202
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-833T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598202 | ||||||
chr15:73598273
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.92-904A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598273 | ||||||
chr15:73598284
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.92-915G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598284 | ||||||
chr15:73598302
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.92-933C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598302 | ||||||
chr15:73598302
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.92-933C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598302 | ||||||
chr15:73598472
|
T | TA | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 34 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.92-1104dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598472 | ||||||
chr15:73598472
|
TA | T | 11 | a0001c0001t0001g0136a0001c0001t0001g0171a0001c0001t0001g0199others(8): Show | 11 | HG00621.hp1 HG00673.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-1104delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598472 | ||||||
chr15:73598695
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.92-1326T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598695 | ||||||
chr15:73598939
|
T | C | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-1570A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598939 | ||||||
chr15:73599192
|
G | GAGCCCCC others(1): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 7 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-1831_92-1824dup others(8): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599192 | ||||||
chr15:73599388
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-2019C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599388 | ||||||
chr15:73599449
|
A | G | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.92-2080T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599449 | ||||||
chr15:73599507
|
G | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.92-2138C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599507 | ||||||
chr15:73599648
|
A | AAGGG | 43 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(40): Show | 49 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.92-2283_92-2280dup others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599648 | ||||||
chr15:73599854
|
C | T | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-2485G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599854 | ||||||
chr15:73600037
|
T | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(51): Show | 63 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.92-2668A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600037 | ||||||
chr15:73600095
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.92-2726A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600095 | ||||||
chr15:73600129
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92-2760T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600129 | ||||||
chr15:73600130
|
G | T | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 34 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.92-2761C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600130 | ||||||
chr15:73600325
|
G | GACATTTT others(9): Show |
72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.92-2957_92-2956ins others(16): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600325 | ||||||
chr15:73600348
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92-2979A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600348 | ||||||
chr15:73600349
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92-2980A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600349 | ||||||
chr15:73600611
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 210 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.92-3242A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600611 | ||||||
chr15:73600647
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-3278A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600647 | ||||||
chr15:73600882
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.92-3513G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600882 | ||||||
chr15:73600940
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3571C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600940 | ||||||
chr15:73600951
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3582C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600951 | ||||||
chr15:73601045
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0287 | 3 | HG01243.hp2 HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.92-3676G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601045 | ||||||
chr15:73601046
|
G | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3677C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601046 | ||||||
chr15:73601278
|
C | T | 10 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(7): Show | 10 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-3909G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601278 | ||||||
chr15:73601283
|
CA | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-3915delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601283 | ||||||
chr15:73601907
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0287a0001c0001t0001g0288 | 4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-4538G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601907 | ||||||
chr15:73601935
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-4566C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601935 | ||||||
chr15:73602179
|
AC | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 333 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(330): Show |
intron_variant | MODIFIER | c.92-4811delG | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602179 | ||||||
chr15:73602377
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-5008G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602377 | ||||||
chr15:73602482
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92-5113C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602482 | ||||||
chr15:73602639
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.92-5270C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602639 | ||||||
chr15:73602833
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.92-5464G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602833 | ||||||
chr15:73602934
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.92-5565G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602934 | ||||||
chr15:73602952
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-5583C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602952 | ||||||
chr15:73602969
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-5600G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602969 | ||||||
chr15:73602989
|
G | C | 26 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(23): Show | 31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.92-5620C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602989 | ||||||
chr15:73602991
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.92-5622C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602991 | ||||||
chr15:73603266
|
T | C | 12 | a0001c0001t0001g0223a0001c0001t0002g0010a0001c0001t0002g0027others(9): Show | 17 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-5897A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603266 | ||||||
chr15:73603314
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-5945C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603314 | ||||||
chr15:73603485
|
A | G | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-6116T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603485 | ||||||
chr15:73603510
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 208 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.92-6141A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603510 | ||||||
chr15:73603511
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.92-6142C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603511 | ||||||
chr15:73603574
|
CAG | C | 12 | a0001c0001t0001g0223a0001c0001t0002g0010a0001c0001t0002g0027others(9): Show | 17 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-6207_92-6206del others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603574 | ||||||
chr15:73603752
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.92-6383A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603752 | ||||||
chr15:73604011
|
G | C | 1 | a0001c0001t0002g0230 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.92-6642C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604011 | ||||||
chr15:73604027
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0113a0001c0001t0001g0120others(1): Show | 5 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-6658C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604027 | ||||||
chr15:73604079
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-6710G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604079 | ||||||
chr15:73604247
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 217 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.92-6878G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604247 | ||||||
chr15:73604268
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92-6899C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604268 | ||||||
chr15:73604328
|
A | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.92-6959T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604328 | ||||||
chr15:73604554
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.92-7185A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604554 | ||||||
chr15:73604667
|
A | G | 11 | a0001c0001t0001g0223a0001c0001t0002g0010a0001c0001t0002g0027others(8): Show | 16 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-7298T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604667 | ||||||
chr15:73605067
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.92-7698G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605067 | ||||||
chr15:73605099
|
A | AG | 18 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0031others(15): Show | 22 | HG00621.hp1 HG01109.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-7731dupC | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605099 | ||||||
chr15:73605099
|
A | AGGCGGGG others(5): Show |
1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-7731_92-7730ins others(12): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605099 | ||||||
chr15:73605099
|
A | AGGGGGGG others(4): Show |
1 | a0001c0002t0001g0283 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-7741_92-7731dup others(11): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605099 | ||||||
chr15:73605102
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-7733C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605102 | ||||||
chr15:73605104
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.92-7735C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605104 | ||||||
chr15:73605104
|
G | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0053 | 5 | HG01891.hp1 NA18948.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-7735C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605104 | ||||||
chr15:73605104
|
G | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0148others(2): Show | 8 | HG00558.hp2 HG00597.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-7735C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605104 | ||||||
chr15:73605110
|
G | GA | 13 | a0001c0001t0001g0004a0001c0001t0001g0223a0001c0001t0001g0238others(10): Show | 20 | HG01496.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-7742_92-7741ins others(1): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605110 | ||||||
chr15:73605111
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 161 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.92-7742C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | ||||||
chr15:73605111
|
G | GA | 11 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0067others(8): Show | 12 | HG00597.hp2 HG01261.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-7743dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | ||||||
chr15:73605111
|
G | GAA | 4 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0273others(1): Show | 4 | HG02071.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-7744_92-7743dup others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | ||||||
chr15:73605111
|
GAA | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287 | 4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-7744_92-7743del others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | ||||||
chr15:73605112
|
A | G | 54 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(51): Show | 59 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.92-7743T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605112 | ||||||
chr15:73605113
|
A | G | 19 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 19 | HG00438.hp1 HG02155.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-7744T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605113 | ||||||
chr15:73605114
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-7745T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605114 | ||||||
chr15:73605170
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.92-7801C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605170 | ||||||
chr15:73605299
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.92-7930A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605299 | ||||||
chr15:73605330
|
T | C | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 26 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-7961A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605330 | ||||||
chr15:73605376
|
T | TA | 10 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 11 | HG00621.hp2 HG02132.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-8008dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605376 | ||||||
chr15:73605394
|
C | T | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(1): Show | 4 | NA18950.hp2 NA19063.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-8025G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605394 | ||||||
chr15:73605435
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92-8066A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605435 | ||||||
chr15:73605454
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-8085A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605454 | ||||||
chr15:73605510
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0214 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.92-8141G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605510 | ||||||
chr15:73605623
|
G | A | 12 | a0001c0001t0001g0223a0001c0001t0002g0010a0001c0001t0002g0027others(9): Show | 17 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-8254C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605623 | ||||||
chr15:73605658
|
G | GC | 49 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 55 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.92-8290_92-8289ins others(1): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605658 | ||||||
chr15:73605726
|
CA | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(90): Show | 110 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.92-8358delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605726 | ||||||
chr15:73605846
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.92-8477T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605846 | ||||||
chr15:73606054
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.92-8685T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606054 | ||||||
chr15:73606373
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.92-9004T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606373 | ||||||
chr15:73606467
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92-9098A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606467 | ||||||
chr15:73606520
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-9151A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606520 | ||||||
chr15:73606701
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-9332C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606701 | ||||||
chr15:73606851
|
C | A | 1 | a0001c0001t0001g0182 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.92-9482G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606851 | ||||||
chr15:73606939
|
CAG | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0123others(3): Show | 7 | HG01243.hp1 HG02109.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-9572_92-9571del others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606939 | ||||||
chr15:73607047
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-9678G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607047 | ||||||
chr15:73607339
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.92-9970C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607339 | ||||||
chr15:73607360
|
A | C | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(4): Show | 7 | HG00438.hp1 HG02155.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-9991T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607360 | ||||||
chr15:73607411
|
C | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.92-10042G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607411 | ||||||
chr15:73607467
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.92-10098G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607467 | ||||||
chr15:73607524
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0149a0001c0001t0001g0183 | 4 | HG02300.hp1 NA18960.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-10155C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607524 | ||||||
chr15:73607694
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-10325A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607694 | ||||||
chr15:73607721
|
A | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-10352T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607721 | ||||||
chr15:73607818
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-10449C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607818 | ||||||
chr15:73607830
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-10461G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607830 | ||||||
chr15:73607878
|
G | A | 1 | a0001c0001t0003g0038 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.92-10509C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607878 | ||||||
chr15:73607951
|
T | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.92-10582A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607951 | ||||||
chr15:73607966
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 7 | HG01346.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-10597A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607966 | ||||||
chr15:73608022
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.92-10653A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608022 | ||||||
chr15:73608063
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.92-10694A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608063 | ||||||
chr15:73608071
|
C | A | 1 | a0001c0001t0001g0016 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.92-10702G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608071 | ||||||
chr15:73608382
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92-11013A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608382 | ||||||
chr15:73608511
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.92-11142A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608511 | ||||||
chr15:73608629
|
A | ATTCTAAA others(9): Show |
72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.92-11261_92-11260i others(18): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608629 | ||||||
chr15:73608666
|
TCTGA | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0258a0001c0001t0001g0260others(4): Show | 8 | HG02015.hp2 HG02083.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11301_92-11298d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608666 | ||||||
chr15:73608822
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92-11453T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608822 | ||||||
chr15:73608854
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.92-11485G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608854 | ||||||
chr15:73609005
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-11636C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609005 | ||||||
chr15:73609201
|
ATATTT | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | NA18969.hp2 NA18975.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-11837_92-11833d others(7): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609201 | ||||||
chr15:73609317
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01261.hp1 HG01496.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.92-11948C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609317 | ||||||
chr15:73609409
|
TCACCTGA others(5): Show |
T | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-12052_92-12041d others(14): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609409 | ||||||
chr15:73609472
|
A | G | 1 | a0001c0001t0005g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.92-12103T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609472 | ||||||
chr15:73609633
|
A | AAAAC | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-12268_92-12265d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609633 | ||||||
chr15:73609675
|
C | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 341 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(338): Show |
intron_variant | MODIFIER | c.92-12306G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609675 | ||||||
chr15:73609798
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0287 | 3 | HG01243.hp2 HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.92-12429A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609798 | ||||||
chr15:73609948
|
T | A | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-12579A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609948 | ||||||
chr15:73610005
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.92-12636G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610005 | ||||||
chr15:73610090
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.92-12721A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610090 | ||||||
chr15:73610093
|
T | C | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-12724A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610093 | ||||||
chr15:73610770
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.92-13401G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610770 | ||||||
chr15:73611045
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.92-13676A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611045 | ||||||
chr15:73611238
|
T | G | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-13869A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611238 | ||||||
chr15:73611320
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.92-13951A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611320 | ||||||
chr15:73611554
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.92-14185A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611554 | ||||||
chr15:73611649
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-14280A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611649 | ||||||
chr15:73611680
|
T | C | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-14311A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611680 | ||||||
chr15:73611726
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-14357G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611726 | ||||||
chr15:73611749
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-14380C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611749 | ||||||
chr15:73611943
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-14574C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611943 | ||||||
chr15:73612151
|
T | G | 1 | a0001c0001t0001g0064 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.92-14782A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612151 | ||||||
chr15:73612409
|
G | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-15040C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612409 | ||||||
chr15:73612420
|
CA | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 214 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(211): Show |
intron_variant | MODIFIER | c.92-15052delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612420 | ||||||
chr15:73612441
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.92-15072T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612441 | ||||||
chr15:73612494
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-15125C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612494 | ||||||
chr15:73612533
|
C | T | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.92-15164G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612533 | ||||||
chr15:73612583
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 210 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.92-15214A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612583 | ||||||
chr15:73612901
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.92-15532G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612901 | ||||||
chr15:73613411
|
A | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG01192.hp2 HG01258.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-16042T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613411 | ||||||
chr15:73613664
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-16295C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613664 | ||||||
chr15:73613671
|
G | A | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-16302C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613671 | ||||||
chr15:73613716
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.92-16347G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613716 | ||||||
chr15:73613977
|
T | G | 1 | a0001c0001t0001g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-16608A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613977 | ||||||
chr15:73614081
|
G | A | 1 | a0001c0001t0001g0019 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.92-16712C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614081 | ||||||
chr15:73614157
|
C | CA | 12 | a0001c0001t0001g0035a0001c0001t0001g0187a0001c0001t0001g0188others(9): Show | 13 | HG00673.hp1 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-16789dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614157 | ||||||
chr15:73614173
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-16804T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614173 | ||||||
chr15:73614319
|
T | TA | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(113): Show | 139 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.92-16951dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614319 | ||||||
chr15:73614319
|
TA | T | 11 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-16951delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614319 | ||||||
chr15:73614366
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(58): Show | 77 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.92-16997T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614366 | ||||||
chr15:73614544
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-17175T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614544 | ||||||
chr15:73614687
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-17318A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614687 | ||||||
chr15:73614698
|
GA | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-17330delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614698 | ||||||
chr15:73614772
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.92-17403T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614772 | ||||||
chr15:73615025
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-17656A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615025 | ||||||
chr15:73615098
|
G | C | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-17729C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615098 | ||||||
chr15:73615100
|
T | TGGA | 3 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0105 | 5 | NA18948.hp1 NA18964.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-17734_92-17732d others(5): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615100 | ||||||
chr15:73615104
|
T | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-17735A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615104 | ||||||
chr15:73615156
|
C | CT | 15 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 20 | HG00673.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-17788dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615156 | ||||||
chr15:73615156
|
CT | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 81 | HG00438.hp1 HG00639.hp1 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.92-17788delA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615156 | ||||||
chr15:73615173
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.92-17804A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615173 | ||||||
chr15:73615174
|
A | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0053 | 2 | HG00639.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.92-17805T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615174 | ||||||
chr15:73615315
|
A | G | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+17810T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615315 | ||||||
chr15:73615350
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.91+17775T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615350 | ||||||
chr15:73615663
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+17462A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615663 | ||||||
chr15:73615824
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.91+17301A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615824 | ||||||
chr15:73615871
|
A | G | 50 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(47): Show | 56 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+17254T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615871 | ||||||
chr15:73615980
|
A | G | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+17145T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615980 | ||||||
chr15:73616038
|
A | AT | 3 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143 | 5 | HG02145.hp1 HG02622.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+17086dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616038 | ||||||
chr15:73616407
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.91+16718C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616407 | ||||||
chr15:73616447
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+16678G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616447 | ||||||
chr15:73616462
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.91+16663C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616462 | ||||||
chr15:73616529
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.91+16596G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616529 | ||||||
chr15:73616534
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+16591C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616534 | ||||||
chr15:73616579
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.91+16546G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616579 | ||||||
chr15:73616593
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.91+16532T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616593 | ||||||
chr15:73616618
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+16507G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616618 | ||||||
chr15:73616676
|
C | G | 1 | a0001c0001t0001g0013 | 2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.91+16449G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616676 | ||||||
chr15:73617456
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.91+15669A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73617456 | ||||||
chr15:73617466
|
T | G | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 34 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.91+15659A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73617466 | ||||||
chr15:73617949
|
A | G | 12 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(9): Show | 12 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+15176T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73617949 | ||||||
chr15:73618033
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 211 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.91+15092T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618033 | ||||||
chr15:73618048
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00280.hp2 HG01081.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.91+15077C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618048 | ||||||
chr15:73618158
|
C | A | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+14967G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618158 | ||||||
chr15:73618174
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+14951T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618174 | ||||||
chr15:73618467
|
A | T | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+14658T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618467 | ||||||
chr15:73618506
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.91+14619A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618506 | ||||||
chr15:73618703
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.91+14422C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618703 | ||||||
chr15:73618959
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG00673.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.91+14166A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618959 | ||||||
chr15:73618962
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.91+14163C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618962 | ||||||
chr15:73618991
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.91+14134G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618991 | ||||||
chr15:73619062
|
C | CA | 24 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0132others(21): Show | 31 | HG01496.hp2 HG01952.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.91+14062dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619062 | ||||||
chr15:73619062
|
CA | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0142others(16): Show | 21 | HG00438.hp1 HG01346.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.91+14062delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619062 | ||||||
chr15:73619456
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.91+13669T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619456 | ||||||
chr15:73619808
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.91+13317G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619808 | ||||||
chr15:73619979
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+13146C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619979 | ||||||
chr15:73620033
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+13092A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620033 | ||||||
chr15:73620165
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.91+12960C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620165 | ||||||
chr15:73620272
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+12853G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620272 | ||||||
chr15:73620403
|
A | G | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.91+12722T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620403 | ||||||
chr15:73620655
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91+12470A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620655 | ||||||
chr15:73620817
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.91+12308A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620817 | ||||||
chr15:73620854
|
G | GT | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+12270dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620854 | ||||||
chr15:73620897
|
C | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 217 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.91+12228G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620897 | ||||||
chr15:73621099
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.91+12026A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621099 | ||||||
chr15:73621231
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.91+11894G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621231 | ||||||
chr15:73621332
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.91+11793A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621332 | ||||||
chr15:73621497
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91+11628T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621497 | ||||||
chr15:73621681
|
C | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+11444G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621681 | ||||||
chr15:73621748
|
C | T | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 26 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.91+11377G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621748 | ||||||
chr15:73621778
|
C | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+11347G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621778 | ||||||
chr15:73621914
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+11211T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621914 | ||||||
chr15:73622022
|
G | T | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+11103C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622022 | ||||||
chr15:73622048
|
G | A | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.91+11077C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622048 | ||||||
chr15:73622107
|
C | T | 1 | a0001c0001t0001g0257 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.91+11018G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622107 | ||||||
chr15:73622114
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.91+11011T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622114 | ||||||
chr15:73622170
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.91+10955G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622170 | ||||||
chr15:73622423
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.91+10702T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622423 | ||||||
chr15:73622451
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.91+10674T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622451 | ||||||
chr15:73622499
|
T | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0232a0001c0001t0001g0233others(9): Show | 13 | HG02055.hp2 HG02293.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+10626A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622499 | ||||||
chr15:73622625
|
T | C | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG00673.hp2 NA18955.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+10500A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622625 | ||||||
chr15:73622725
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.91+10400A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622725 | ||||||
chr15:73622777
|
C | G | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+10348G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622777 | ||||||
chr15:73622886
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+10239C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622886 | ||||||
chr15:73622891
|
T | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.91+10234A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622891 | ||||||
chr15:73622901
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.91+10224A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622901 | ||||||
chr15:73622913
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 121 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.91+10212G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622913 | ||||||
chr15:73623115
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+10010G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623115 | ||||||
chr15:73623123
|
A | G | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(4): Show | 7 | HG00438.hp1 HG02155.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10002T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623123 | ||||||
chr15:73623138
|
T | A | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+9987A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623138 | ||||||
chr15:73623453
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+9672G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623453 | ||||||
chr15:73623479
|
G | A | 8 | a0001c0001t0001g0047a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01261.hp2 HG01975.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+9646C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623479 | ||||||
chr15:73623696
|
C | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+9429G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623696 | ||||||
chr15:73623796
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91+9329A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623796 | ||||||
chr15:73623811
|
A | T | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+9314T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623811 | ||||||
chr15:73623849
|
CCTA | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+9273_91+9275del others(3): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623849 | ||||||
chr15:73623896
|
C | T | 1 | a0001c0001t0002g0226 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91+9229G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623896 | ||||||
chr15:73623979
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.91+9146A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623979 | ||||||
chr15:73624042
|
A | G | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.91+9083T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624042 | ||||||
chr15:73624161
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.91+8964C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624161 | ||||||
chr15:73624336
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.91+8789A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624336 | ||||||
chr15:73624638
|
T | TA | 35 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 41 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.91+8486dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624638 | ||||||
chr15:73624648
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 81 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.91+8477G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624648 | ||||||
chr15:73624677
|
C | T | 1 | a0001c0001t0001g0257 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.91+8448G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624677 | ||||||
chr15:73624834
|
A | G | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+8291T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624834 | ||||||
chr15:73624946
|
C | A | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+8179G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624946 | ||||||
chr15:73625009
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+8116T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625009 | ||||||
chr15:73625035
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+8090A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625035 | ||||||
chr15:73625133
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.91+7992G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625133 | ||||||
chr15:73625353
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91+7772T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625353 | ||||||
chr15:73625378
|
T | C | 26 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(23): Show | 31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+7747A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625378 | ||||||
chr15:73625428
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.91+7697C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625428 | ||||||
chr15:73625506
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.91+7619A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625506 | ||||||
chr15:73625521
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+7604A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625521 | ||||||
chr15:73625567
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+7558C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625567 | ||||||
chr15:73625633
|
G | C | 27 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(24): Show | 32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.91+7492C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625633 | ||||||
chr15:73625685
|
T | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+7440A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625685 | ||||||
chr15:73625972
|
A | G | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+7153T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625972 | ||||||
chr15:73626147
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+6978C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626147 | ||||||
chr15:73626157
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+6968C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626157 | ||||||
chr15:73626331
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.91+6794C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626331 | ||||||
chr15:73626431
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+6694C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626431 | ||||||
chr15:73626452
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.91+6673G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626452 | ||||||
chr15:73626458
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+6667T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626458 | ||||||
chr15:73626636
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.91+6489A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626636 | ||||||
chr15:73627107
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.91+6018G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73627107 | ||||||
chr15:73627784
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+5341A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73627784 | ||||||
chr15:73628125
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+5000C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628125 | ||||||
chr15:73628227
|
C | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18974.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.91+4898G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628227 | ||||||
chr15:73628229
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | 34 | HG00609.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.91+4896T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628229 | ||||||
chr15:73628260
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.91+4865C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628260 | ||||||
chr15:73628388
|
T | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4737A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628388 | ||||||
chr15:73628528
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.91+4597G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628528 | ||||||
chr15:73628607
|
C | G | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+4518G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628607 | ||||||
chr15:73628866
|
C | G | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+4259G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628866 | ||||||
chr15:73629079
|
C | T | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.91+4046G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629079 | ||||||
chr15:73629141
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+3984C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629141 | ||||||
chr15:73629147
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+3978A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629147 | ||||||
chr15:73629216
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+3909T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629216 | ||||||
chr15:73629233
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+3892C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629233 | ||||||
chr15:73629479
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+3646G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629479 | ||||||
chr15:73629655
|
T | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(69): Show | 86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.91+3470A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629655 | ||||||
chr15:73629851
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.91+3274T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629851 | ||||||
chr15:73630019
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0028others(7): Show | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+3106C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630019 | ||||||
chr15:73630026
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.91+3099A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630026 | ||||||
chr15:73630185
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.91+2940T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630185 | ||||||
chr15:73630214
|
G | C | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+2911C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630214 | ||||||
chr15:73630266
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.91+2859G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630266 | ||||||
chr15:73630402
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+2723G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630402 | ||||||
chr15:73630411
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.91+2714T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630411 | ||||||
chr15:73630572
|
T | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(46): Show | 58 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.91+2553A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630572 | ||||||
chr15:73630630
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+2495T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630630 | ||||||
chr15:73630667
|
A | G | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG00438.hp1 HG04184.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+2458T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630667 | ||||||
chr15:73630830
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.91+2295A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630830 | ||||||
chr15:73630888
|
G | C | 2 | a0001c0002t0001g0283a0001c0002t0001g0284 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+2237C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630888 | ||||||
chr15:73630927
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+2198A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630927 | ||||||
chr15:73631248
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.91+1877A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631248 | ||||||
chr15:73631432
|
C | G | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+1693G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631432 | ||||||
chr15:73631509
|
C | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.91+1616G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631509 | ||||||
chr15:73631711
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0006g0289 | 2 | HG01346.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.91+1414G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631711 | ||||||
chr15:73631881
|
C | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.91+1244G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631881 | ||||||
chr15:73631932
|
A | G | 1 | a0001c0001t0001g0030 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.91+1193T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631932 | ||||||
chr15:73632110
|
G | A | 46 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 52 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.91+1015C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632110 | ||||||
chr15:73632538
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+587A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632538 | ||||||
chr15:73632931
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.91+194C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632931 | ||||||
chr15:73632961
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+164G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632961 | ||||||
chr15:73633052
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+73C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73633052 | ||||||
chr15:73633059
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.91+66C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73633059 |