geneid | 57185 |
---|---|
ensemblid | ENSG00000001461.17 |
hgncid | 25233 |
symbol | NIPAL3 |
name | NIPA like domain containing 3 |
refseq_nuc | NM_020448.5 |
refseq_prot | NP_065181.1 |
ensembl_nuc | ENST00000374399.9 |
ensembl_prot | ENSP00000363520.4 |
mane_status | MANE Select |
chr | chr1 |
start | 24415802 |
end | 24472976 |
strand | + |
ver | v1.2 |
region | chr1:24415802-24472976 |
region5000 | chr1:24410802-24477976 |
regionname0 | NIPAL3_chr1_24415802_24472976 |
regionname5000 | NIPAL3_chr1_24410802_24477976 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 406 | 377 | 87 | 68 | 162 | 16 | 42 | 122 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0002 | 0/0 | 406 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0003 | 0/0 | 196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0004 | 0/0 | 406 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1221 | 241 | 70 | 46 | 89 | 10 | 25 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0002 | 0/1 | 1221 | 121 | 14 | 22 | 61 | 6 | 17 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0003 | 0/0 | 1221 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0004 | 0/0 | 1221 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0005 | 0/0 | 1221 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0006 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0007 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0008 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0009 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
c0010 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4152 | 89 | 3 | 13 | 53 | 4 | 15 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0002 | 1/0 | 4152 | 53 | 6 | 6 | 23 | 5 | 12 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0003 | 0/0 | 4152 | 50 | 6 | 12 | 26 | 2 | 4 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0004 | 0/0 | 4151 | 24 | 21 | 2 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0005 | 0/0 | 4152 | 12 | 0 | 0 | 12 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0006 | 0/0 | 4151 | 9 | 4 | 0 | 1 | 2 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0007 | 0/0 | 4151 | 8 | 7 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0008 | 0/0 | 4152 | 8 | 0 | 5 | 0 | 2 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0009 | 0/0 | 4152 | 6 | 0 | 6 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0010 | 0/0 | 4152 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0011 | 0/0 | 4151 | 5 | 2 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0012 | 0/0 | 4152 | 5 | 0 | 2 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0013 | 0/0 | 4151 | 4 | 2 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0014 | 0/0 | 4152 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0015 | 0/0 | 4153 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0016 | 0/0 | 4150 | 4 | 1 | 1 | 0 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0017 | 0/0 | 4154 | 4 | 1 | 3 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0018 | 0/0 | 4152 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0019 | 0/0 | 4153 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0020 | 0/0 | 4151 | 4 | 3 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0021 | 0/0 | 4154 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0022 | 0/0 | 4151 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0023 | 0/0 | 4152 | 3 | 0 | 0 | 2 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0024 | 0/0 | 4151 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0025 | 0/0 | 4152 | 2 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0026 | 0/0 | 4152 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0027 | 0/0 | 4153 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0028 | 0/0 | 4151 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0029 | 0/0 | 4150 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0030 | 0/0 | 4151 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0031 | 0/0 | 4153 | 2 | 0 | 0 | 1 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0032 | 0/0 | 4151 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0033 | 0/0 | 4153 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0034 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0035 | 0/0 | 4153 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0036 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0037 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0038 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0039 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0040 | 0/0 | 4153 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0041 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0042 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0043 | 0/0 | 4152 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0044 | 0/0 | 4154 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0045 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0046 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0047 | 0/0 | 4154 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0048 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0049 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0050 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0051 | 0/0 | 4150 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0052 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0053 | 0/0 | 4152 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0054 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0055 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0056 | 0/0 | 4150 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0057 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0058 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0059 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0060 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0061 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0062 | 0/0 | 4151 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0063 | 0/0 | 4153 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0064 | 0/0 | 4150 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0065 | 0/0 | 4150 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0066 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0067 | 0/0 | 4151 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0068 | 0/0 | 4150 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0069 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0070 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0071 | 0/0 | 4153 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0072 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0073 | 0/0 | 4150 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0074 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0075 | 0/0 | 4152 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0076 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
t0077 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1221 | 241 | 70 | 46 | 89 | 10 | 25 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002 | 0/1 | 1221 | 121 | 14 | 22 | 61 | 6 | 17 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0003 | 0/0 | 1221 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0004 | 0/0 | 1221 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0005 | 0/0 | 1221 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0008 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0010 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0002c0007 | 0/0 | 1221 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0003c0009 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0004c0006 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5372 | 50 | 2 | 5 | 34 | 2 | 7 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0002 | 1/0 | 5372 | 45 | 6 | 6 | 17 | 5 | 10 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0003 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0004 | 0/0 | 5371 | 21 | 18 | 2 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0005 | 0/0 | 5372 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0006 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0007 | 0/0 | 5371 | 8 | 7 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0008 | 0/0 | 5372 | 8 | 0 | 5 | 0 | 2 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0009 | 0/0 | 5372 | 6 | 0 | 6 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0010 | 0/0 | 5372 | 6 | 0 | 0 | 6 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0011 | 0/0 | 5371 | 5 | 2 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0012 | 0/0 | 5372 | 3 | 0 | 1 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0013 | 0/0 | 5371 | 4 | 2 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0014 | 0/0 | 5372 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0015 | 0/0 | 5373 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0016 | 0/0 | 5370 | 4 | 1 | 1 | 0 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0017 | 0/0 | 5374 | 4 | 1 | 3 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0018 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0020 | 0/0 | 5371 | 4 | 3 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0021 | 0/0 | 5374 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0022 | 0/0 | 5371 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0023 | 0/0 | 5372 | 2 | 0 | 0 | 1 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0024 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0025 | 0/0 | 5372 | 2 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0027 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0028 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0029 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0030 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0031 | 0/0 | 5373 | 2 | 0 | 0 | 1 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0032 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0034 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0035 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0037 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0038 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0039 | 0/0 | 5383 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0040 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0041 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0042 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0043 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0046 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0047 | 0/0 | 5374 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0049 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0050 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0051 | 0/0 | 5370 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0052 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0053 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0054 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0055 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0056 | 0/0 | 5370 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0057 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0059 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0060 | 0/0 | 5374 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0064 | 0/0 | 5370 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0065 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0066 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0068 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0069 | 0/0 | 5372 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0071 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0072 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0073 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0074 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0075 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0076 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0001t0077 | 0/0 | 5371 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0001 | 0/1 | 5372 | 38 | 1 | 8 | 18 | 2 | 8 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0002 | 0/0 | 5372 | 8 | 0 | 0 | 6 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0003 | 0/0 | 5372 | 41 | 6 | 12 | 17 | 2 | 4 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0005 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0006 | 0/0 | 5371 | 8 | 3 | 0 | 1 | 2 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0012 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0015 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0018 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0019 | 0/0 | 5373 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0023 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0026 | 0/0 | 5372 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0027 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0028 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0033 | 0/0 | 5373 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0036 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0044 | 0/0 | 5374 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0045 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0048 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0058 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0061 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0062 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0063 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0002t0067 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0003t0001 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0003t0003 | 0/0 | 5372 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0004t0005 | 0/0 | 5372 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0005t0004 | 0/0 | 5371 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0008t0003 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0001c0010t0003 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0002c0007t0029 | 0/0 | 5370 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0003c0009t0012 | 0/0 | 5372 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
a0004c0006t0070 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | copy fasta | chr1 | 24410802 | 24477976 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0008g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0009g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0010g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0012g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0012g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0013g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0015g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0015g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0015g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0016g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0016g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0016g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0017g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0017g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0018g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0020g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0021g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0021g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0021g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0022g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0022g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0022g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0023g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0023g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0024g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0024g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0025g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0027g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0029g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0030g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0030g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0031g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0031g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0032g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0032g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0034g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0035g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0037g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0038g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0039g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0040g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0041g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0042g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0043g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0046g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0047g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0049g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0050g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0051g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0052g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0053g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0054g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0055g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0056g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0057g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0059g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0060g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0064g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0065g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0066g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0068g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0069g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0071g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0072g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0073g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0074g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0075g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0076g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0001t0077g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0012g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0015g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0018g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0018g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0019g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0023g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0026g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0026g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0027g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0028g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0033g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0033g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0036g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0044g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0045g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0048g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0058g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0061g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0062g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0063g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0002t0067g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0004t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0005t0004g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0008t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0001c0010t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0002c0007t0029g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0003c0009t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
a0004c0006t0070g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0068 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0064 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0069 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00438 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00544 | hp2 | a0001 | c0001 | t0018 | g0007 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0296 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0226 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00609 | hp2 | a0001 | c0008 | t0003 | g0312 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0066 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0327 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00639 | hp2 | a0001 | c0001 | t0064 | g0140 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00673 | hp1 | a0001 | c0001 | t0012 | g0323 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | CHS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0185 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0310 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00741 | hp1 | a0001 | c0001 | t0047 | g0165 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01069 | hp1 | a0001 | c0001 | t0013 | g0193 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01069 | hp2 | a0001 | c0001 | t0017 | g0026 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01070 | hp1 | a0001 | c0001 | t0008 | g0023 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0258 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01071 | hp2 | a0001 | c0001 | t0017 | g0026 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01081 | hp2 | a0001 | c0001 | t0025 | g0015 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01099 | hp1 | a0001 | c0001 | t0020 | g0158 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0086 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01106 | hp1 | a0001 | c0001 | t0035 | g0145 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01106 | hp2 | a0001 | c0002 | t0012 | g0262 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01109 | hp1 | a0001 | c0001 | t0016 | g0168 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01109 | hp2 | a0001 | c0001 | t0037 | g0191 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0232 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01168 | hp2 | a0001 | c0001 | t0076 | g0293 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01175 | hp2 | a0001 | c0001 | t0077 | g0178 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01192 | hp1 | a0001 | c0001 | t0043 | g0244 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01192 | hp2 | a0001 | c0001 | t0053 | g0169 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01243 | hp1 | a0001 | c0001 | t0059 | g0018 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01243 | hp2 | a0001 | c0001 | t0017 | g0263 | AMR | PUR | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0302 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01255 | hp2 | a0001 | c0001 | t0051 | g0166 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01257 | hp1 | a0001 | c0001 | t0008 | g0266 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01257 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01346 | hp1 | a0001 | c0001 | t0056 | g0245 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0295 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0095 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0200 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01496 | hp2 | a0001 | c0001 | t0075 | g0291 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01515 | hp2 | a0001 | c0001 | t0008 | g0294 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0292 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0058 | EUR | IBS | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01884 | hp1 | a0001 | c0002 | t0033 | g0179 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01891 | hp1 | a0001 | c0005 | t0004 | g0003 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01952 | hp1 | a0001 | c0002 | t0044 | g0022 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0221 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0051 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01975 | hp2 | a0001 | c0001 | t0009 | g0222 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0050 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01993 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0093 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02004 | hp2 | a0001 | c0001 | t0008 | g0023 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02027 | hp1 | a0001 | c0003 | t0003 | g0090 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02056 | hp1 | a0001 | c0001 | t0060 | g0214 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02056 | hp2 | a0001 | c0001 | t0046 | g0321 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02074 | hp1 | a0001 | c0010 | t0003 | g0227 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0183 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02083 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02129 | hp2 | a0001 | c0002 | t0018 | g0220 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02145 | hp1 | a0001 | c0001 | t0074 | g0033 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0102 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02257 | hp1 | a0001 | c0001 | t0022 | g0264 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02258 | hp1 | a0001 | c0001 | t0024 | g0195 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02258 | hp2 | a0001 | c0001 | t0032 | g0159 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02273 | hp2 | a0001 | c0001 | t0009 | g0233 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02280 | hp1 | a0001 | c0002 | t0036 | g0047 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02280 | hp2 | a0001 | c0001 | t0024 | g0194 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02300 | hp1 | a0001 | c0001 | t0009 | g0236 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0100 | AMR | PEL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02451 | hp1 | a0001 | c0001 | t0050 | g0162 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0129 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02523 | hp2 | a0001 | c0002 | t0018 | g0116 | EAS | KHV | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02615 | hp2 | a0001 | c0001 | t0020 | g0157 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0003 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0155 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0330 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02723 | hp2 | a0001 | c0001 | t0068 | g0184 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02735 | hp1 | a0001 | c0002 | t0006 | g0104 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02809 | hp1 | a0001 | c0001 | t0052 | g0175 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02818 | hp2 | a0001 | c0002 | t0045 | g0149 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02886 | hp1 | a0001 | c0001 | t0055 | g0030 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0091 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02896 | hp2 | a0001 | c0002 | t0006 | g0255 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0190 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02965 | hp1 | a0001 | c0001 | t0013 | g0196 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02965 | hp2 | a0001 | c0001 | t0022 | g0031 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02970 | hp2 | a0001 | c0001 | t0032 | g0163 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02976 | hp2 | a0001 | c0001 | t0038 | g0201 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03041 | hp2 | a0001 | c0001 | t0029 | g0161 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03098 | hp2 | a0001 | c0001 | t0021 | g0329 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03139 | hp2 | a0001 | c0005 | t0004 | g0003 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03195 | hp2 | a0001 | c0001 | t0065 | g0141 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0109 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03209 | hp2 | a0001 | c0001 | t0030 | g0139 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03225 | hp1 | a0001 | c0001 | t0049 | g0259 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03239 | hp1 | a0001 | c0001 | t0069 | g0247 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03453 | hp2 | a0001 | c0002 | t0033 | g0180 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03486 | hp1 | a0001 | c0001 | t0020 | g0034 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03490 | hp1 | a0001 | c0001 | t0016 | g0016 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03492 | hp1 | a0001 | c0001 | t0016 | g0016 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03516 | hp1 | a0001 | c0001 | t0016 | g0167 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03516 | hp2 | a0001 | c0001 | t0021 | g0332 | AFR | ESN | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03540 | hp2 | a0001 | c0001 | t0072 | g0172 | AFR | GWD | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03579 | hp1 | a0001 | c0001 | t0039 | g0189 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03688 | hp2 | a0001 | c0002 | t0063 | g0085 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03710 | hp2 | a0001 | c0001 | t0008 | g0241 | SAS | PJL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03942 | hp1 | a0001 | c0001 | t0025 | g0015 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04115 | hp1 | a0001 | c0001 | t0040 | g0269 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04199 | hp1 | a0001 | c0001 | t0031 | g0204 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04199 | hp2 | a0001 | c0001 | t0071 | g0021 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0059 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04228 | hp1 | a0001 | c0002 | t0006 | g0079 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0117 | SAS | STU | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18522 | hp1 | a0001 | c0001 | t0073 | g0036 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18522 | hp2 | a0001 | c0001 | t0057 | g0006 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18612 | hp1 | a0001 | c0003 | t0003 | g0038 | EAS | CHB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18940 | hp1 | a0001 | c0002 | t0019 | g0010 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18942 | hp2 | a0001 | c0002 | t0028 | g0061 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18943 | hp1 | a0001 | c0001 | t0014 | g0268 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18946 | hp1 | a0001 | c0004 | t0005 | g0240 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18950 | hp2 | a0001 | c0002 | t0003 | g0318 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18952 | hp1 | a0001 | c0002 | t0058 | g0039 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18952 | hp2 | a0001 | c0001 | t0027 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18953 | hp1 | a0001 | c0001 | t0015 | g0285 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18953 | hp2 | a0001 | c0001 | t0023 | g0209 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18956 | hp1 | a0001 | c0002 | t0019 | g0301 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18956 | hp2 | a0003 | c0009 | t0012 | g0094 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18960 | hp1 | a0001 | c0002 | t0026 | g0087 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18963 | hp2 | a0001 | c0002 | t0023 | g0067 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18964 | hp1 | a0001 | c0001 | t0014 | g0284 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18964 | hp2 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18967 | hp2 | a0001 | c0002 | t0019 | g0096 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18968 | hp1 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18970 | hp1 | a0001 | c0001 | t0014 | g0325 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18970 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18972 | hp2 | a0001 | c0004 | t0005 | g0254 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18973 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18975 | hp2 | a0001 | c0002 | t0067 | g0224 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18979 | hp1 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18979 | hp2 | a0001 | c0001 | t0041 | g0280 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18986 | hp1 | a0001 | c0002 | t0061 | g0108 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18986 | hp2 | a0001 | c0004 | t0005 | g0217 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18990 | hp1 | a0001 | c0001 | t0015 | g0298 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18994 | hp1 | a0001 | c0002 | t0048 | g0120 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19000 | hp1 | a0001 | c0003 | t0003 | g0076 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19000 | hp2 | a0004 | c0006 | t0070 | g0009 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19004 | hp1 | a0001 | c0002 | t0005 | g0048 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19004 | hp2 | a0001 | c0001 | t0042 | g0319 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19010 | hp1 | a0001 | c0002 | t0026 | g0012 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19010 | hp2 | a0001 | c0003 | t0003 | g0077 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19011 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19012 | hp2 | a0001 | c0001 | t0066 | g0135 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19043 | hp1 | a0001 | c0001 | t0030 | g0142 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19043 | hp2 | a0002 | c0007 | t0029 | g0174 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19058 | hp1 | a0001 | c0001 | t0012 | g0041 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19058 | hp2 | a0001 | c0002 | t0005 | g0099 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0320 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19063 | hp1 | a0001 | c0002 | t0027 | g0065 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19063 | hp2 | a0001 | c0004 | t0005 | g0223 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19067 | hp2 | a0001 | c0002 | t0015 | g0046 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0208 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19074 | hp2 | a0001 | c0002 | t0062 | g0062 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19078 | hp1 | a0001 | c0002 | t0019 | g0037 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19078 | hp2 | a0001 | c0001 | t0010 | g0210 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19090 | hp2 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0132 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0176 | AFR | YRI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20129 | hp1 | a0001 | c0001 | t0054 | g0331 | AFR | ASW | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ASW | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20752 | hp1 | a0001 | c0001 | t0023 | g0238 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20752 | hp2 | a0001 | c0002 | t0006 | g0106 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0212 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20805 | hp2 | a0001 | c0002 | t0006 | g0103 | EUR | TSI | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0072 | SAS | GIH | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0083 | SAS | GIH | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0081 | AMR | CLM | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0192 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02109 | hp2 | a0001 | c0001 | t0034 | g0328 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG02486 | hp2 | a0001 | c0001 | t0020 | g0160 | AFR | ACB | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | MSL | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0130 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | USA | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA21309 | hp1 | a0001 | c0001 | t0022 | g0032 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | LWK | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0054 | REF | REF | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0211 | REF | REF | NIPAL3_chr1_24410802_24477976 | NIPAL3 | chr1 | 24410802 | 24477976 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24419566
|
G | A | 1 | a0004 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.19G>A | p.Ala7Thr | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/12 | 379/5372 | 19/1221 | 7/406 | chr1 | 24419566 | ||
chr1:24442071
|
G | A | 1 | a0002 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.179G>A | p.Arg60His | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/12 | 539/5372 | 179/1221 | 60/406 | chr1 | 24442071 | ||
chr1:24453456
|
A | T | 1 | a0003 | 1 | NA18956.hp2 | stop_gained | HIGH | c.589A>T | p.Lys197* | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/12 | 949/5372 | 589/1221 | 197/406 | chr1 | 24453456 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24419637
|
C | T | 2 | a0001c0004a0001c0010 | 5 | HG02074.hp1 NA18946.hp1 NA18972.hp2 others(2): Show |
synonymous_variant | LOW | c.90C>T | p.Tyr30Tyr | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/12 | 450/5372 | 90/1221 | 30/406 | chr1 | 24419637 | ||
chr1:24456220
|
C | T | 1 | a0001c0003 | 6 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(3): Show |
synonymous_variant | LOW | c.720C>T | p.Pro240Pro | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/12 | 1080/5372 | 720/1221 | 240/406 | chr1 | 24456220 | ||
chr1:24456256
|
C | T | 1 | a0001c0008 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.756C>T | p.Thr252Thr | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/12 | 1116/5372 | 756/1221 | 252/406 | chr1 | 24456256 | ||
chr1:24458903
|
C | T | 5 | a0001c0002a0001c0003a0001c0008others(2): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
synonymous_variant | LOW | c.789C>T | p.Ala263Ala | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/12 | 1149/5372 | 789/1221 | 263/406 | chr1 | 24458903 | ||
chr1:24469140
|
C | T | 1 | a0001c0005 | 3 | HG01891.hp1 HG02647.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.1176C>T | p.Ala392Ala | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1536/5372 | 1176/1221 | 392/406 | chr1 | 24469140 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24415834
|
C | T | 2 | a0001c0001t0077a0001c0002t0033 | 3 | HG01175.hp2 HG01884.hp1 HG03453.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-328C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/12 | chr1 | 24415834 | ||||||
chr1:24469374
|
T | G | 4 | a0001c0001t0013a0001c0001t0024a0001c0001t0034others(1): Show | 8 | HG00639.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*189T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 189 | chr1 | 24469374 | |||||
chr1:24469527
|
T | G | 1 | a0001c0002t0036 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 342 | chr1 | 24469527 | |||||
chr1:24469577
|
G | A | 5 | a0001c0001t0007a0001c0001t0011a0001c0001t0037others(2): Show | 16 | HG00733.hp1 HG01109.hp2 HG02080.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*392G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 392 | chr1 | 24469577 | |||||
chr1:24469579
|
A | C | 3 | a0001c0001t0008a0001c0001t0075a0001c0001t0076 | 10 | HG01070.hp1 HG01168.hp2 HG01255.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 394 | chr1 | 24469579 | |||||
chr1:24469639
|
C | G | 7 | a0001c0001t0020a0001c0001t0024a0001c0001t0032others(4): Show | 12 | HG01099.hp1 HG01106.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*454C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 454 | chr1 | 24469639 | |||||
chr1:24469653
|
G | A | 1 | a0001c0001t0040 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 468 | chr1 | 24469653 | |||||
chr1:24469837
|
G | A | 1 | a0001c0001t0075 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 652 | chr1 | 24469837 | |||||
chr1:24469876
|
GAAGTTAA others(94): Show |
G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*693_*793del | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 693 | INFO_REALIGN_3_PRIME | chr1 | 24469876 | ||||
chr1:24469946
|
A | G | 1 | a0001c0001t0071 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*761A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 761 | chr1 | 24469946 | |||||
chr1:24469997
|
G | C | 3 | a0001c0001t0014a0001c0001t0041a0001c0001t0042 | 6 | NA18943.hp1 NA18964.hp1 NA18970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*812G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 812 | chr1 | 24469997 | |||||
chr1:24470041
|
C | T | 1 | a0004c0006t0070 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 856 | chr1 | 24470041 | |||||
chr1:24470108
|
C | T | 1 | a0001c0001t0069 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 923 | chr1 | 24470108 | |||||
chr1:24470196
|
A | G | 1 | a0001c0001t0034 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1011A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1011 | chr1 | 24470196 | |||||
chr1:24470348
|
A | G | 23 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(20): Show | 82 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1163A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1163 | chr1 | 24470348 | |||||
chr1:24470382
|
A | G | 1 | a0001c0001t0059 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1197 | chr1 | 24470382 | |||||
chr1:24470893
|
A | G | 2 | a0001c0001t0034a0001c0001t0068 | 2 | HG02109.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1708A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1708 | chr1 | 24470893 | |||||
chr1:24470904
|
G | A | 1 | a0001c0001t0043 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1719G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1719 | chr1 | 24470904 | |||||
chr1:24470968
|
C | G | 1 | a0001c0001t0010 | 6 | NA18942.hp1 NA18970.hp2 NA18973.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1783C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1783 | chr1 | 24470968 | |||||
chr1:24471070
|
T | TCGGTATG others(106): Show |
1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888_*1889insTATG others(109): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1889 | INFO_REALIGN_3_PRIME | chr1 | 24471070 | ||||
chr1:24471074
|
A | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1889A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1889 | chr1 | 24471074 | |||||
chr1:24471076
|
C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1891 | chr1 | 24471076 | |||||
chr1:24471077
|
C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1892 | chr1 | 24471077 | |||||
chr1:24471080
|
A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1895A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1895 | chr1 | 24471080 | |||||
chr1:24471081
|
G | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1896 | chr1 | 24471081 | |||||
chr1:24471082
|
C | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1897C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1897 | chr1 | 24471082 | |||||
chr1:24471084
|
C | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1899 | chr1 | 24471084 | |||||
chr1:24471085
|
A | G | 5 | a0001c0001t0005a0001c0001t0042a0001c0002t0005others(2): Show | 14 | HG00408.hp1 HG00609.hp1 NA18946.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1900A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1900 | chr1 | 24471085 | |||||
chr1:24471112
|
T | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1927 | chr1 | 24471112 | |||||
chr1:24471116
|
G | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1931 | chr1 | 24471116 | |||||
chr1:24471120
|
C | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1935C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1935 | chr1 | 24471120 | |||||
chr1:24471122
|
C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1937C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1937 | chr1 | 24471122 | |||||
chr1:24471145
|
A | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1960A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1960 | chr1 | 24471145 | |||||
chr1:24471148
|
T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1963T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1963 | chr1 | 24471148 | |||||
chr1:24471161
|
T | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1976 | chr1 | 24471161 | |||||
chr1:24471163
|
T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1978T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1978 | chr1 | 24471163 | |||||
chr1:24471164
|
A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1979A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1979 | chr1 | 24471164 | |||||
chr1:24471165
|
A | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1980 | chr1 | 24471165 | |||||
chr1:24471166
|
A | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1981 | chr1 | 24471166 | |||||
chr1:24471168
|
T | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1983 | chr1 | 24471168 | |||||
chr1:24471170
|
G | A | 1 | a0001c0001t0037 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1985G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1985 | chr1 | 24471170 | |||||
chr1:24471173
|
T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1988T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1988 | chr1 | 24471173 | |||||
chr1:24471174
|
G | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1989G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1989 | chr1 | 24471174 | |||||
chr1:24471175
|
A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1990A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1990 | chr1 | 24471175 | |||||
chr1:24471177
|
C | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1992C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 1992 | chr1 | 24471177 | |||||
chr1:24471186
|
G | T | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2001G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2001 | chr1 | 24471186 | |||||
chr1:24471247
|
G | C | 5 | a0001c0001t0007a0001c0001t0011a0001c0001t0037others(2): Show | 16 | HG00733.hp1 HG01109.hp2 HG02080.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2062G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2062 | chr1 | 24471247 | |||||
chr1:24471421
|
A | C | 2 | a0001c0001t0018a0001c0002t0018 | 4 | HG00544.hp2 HG02083.hp1 HG02129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2236A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2236 | chr1 | 24471421 | |||||
chr1:24471511
|
G | A | 55 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(52): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2326G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2326 | chr1 | 24471511 | |||||
chr1:24471530
|
A | G | 1 | a0001c0001t0053 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2345A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2345 | chr1 | 24471530 | |||||
chr1:24471578
|
C | CA | 12 | a0001c0001t0028a0001c0001t0031a0001c0001t0034others(9): Show | 13 | HG01106.hp1 HG01168.hp2 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2413dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2414 | INFO_REALIGN_3_PRIME | chr1 | 24471578 | ||||
chr1:24471578
|
C | CAA | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(26): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*2412_*2413dupAA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2414 | INFO_REALIGN_3_PRIME | chr1 | 24471578 | ||||
chr1:24471578
|
C | CAAA | 10 | a0001c0001t0015a0001c0001t0017a0001c0001t0021others(7): Show | 20 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2411_*2413dupAAA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2414 | INFO_REALIGN_3_PRIME | chr1 | 24471578 | ||||
chr1:24471694
|
T | C | 2 | a0001c0001t0022a0001c0001t0055 | 4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2509T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2509 | chr1 | 24471694 | |||||
chr1:24471720
|
C | A | 1 | a0001c0002t0045 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2535C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2535 | chr1 | 24471720 | |||||
chr1:24471746
|
T | C | 2 | a0001c0001t0064a0001c0001t0065 | 2 | HG00639.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2561T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2561 | chr1 | 24471746 | |||||
chr1:24471893
|
C | T | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(36): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*2708C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2708 | chr1 | 24471893 | |||||
chr1:24471906
|
C | T | 1 | a0001c0002t0048 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2721C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2721 | chr1 | 24471906 | |||||
chr1:24471946
|
G | A | 4 | a0001c0001t0029a0001c0001t0050a0001c0001t0064others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2761G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2761 | chr1 | 24471946 | |||||
chr1:24472008
|
CT | C | 33 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(30): Show | 90 | HG00558.hp1 HG00639.hp1 HG00733.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2841delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2841 | INFO_REALIGN_3_PRIME | chr1 | 24472008 | ||||
chr1:24472008
|
CTT | C | 44 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(41): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*2840_*2841delTT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2840 | INFO_REALIGN_3_PRIME | chr1 | 24472008 | ||||
chr1:24472025
|
T | C | 1 | a0001c0001t0051 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2840T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2840 | chr1 | 24472025 | |||||
chr1:24472169
|
C | T | 1 | a0001c0001t0056 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 2984 | chr1 | 24472169 | |||||
chr1:24472206
|
C | T | 5 | a0001c0001t0007a0001c0001t0030a0001c0001t0037others(2): Show | 13 | HG00733.hp1 HG01109.hp2 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3021C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3021 | chr1 | 24472206 | |||||
chr1:24472236
|
G | A | 2 | a0001c0001t0009a0001c0001t0043 | 7 | HG01168.hp1 HG01192.hp1 HG01496.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3051 | chr1 | 24472236 | |||||
chr1:24472290
|
G | A | 1 | a0001c0002t0026 | 2 | NA18960.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3105G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3105 | chr1 | 24472290 | |||||
chr1:24472332
|
A | G | 1 | a0001c0002t0067 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3147A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3147 | chr1 | 24472332 | |||||
chr1:24472379
|
A | C | 2 | a0001c0001t0021a0001c0001t0054 | 4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3194A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3194 | chr1 | 24472379 | |||||
chr1:24472555
|
A | T | 15 | a0001c0001t0016a0001c0001t0018a0001c0001t0022others(12): Show | 24 | HG00544.hp2 HG01081.hp2 HG01109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3370A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3370 | chr1 | 24472555 | |||||
chr1:24472741
|
G | A | 1 | a0001c0001t0046 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3556 | chr1 | 24472741 | |||||
chr1:24472887
|
C | G | 1 | a0001c0001t0057 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3702C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 12/12 | 3702 | chr1 | 24472887 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:24415925
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-258+21G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24415925 | ||||||
chr1:24416308
|
C | G | 5 | a0001c0001t0017g0026a0001c0001t0021g0329a0001c0001t0021g0330others(2): Show | 6 | HG01069.hp2 HG01071.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-258+404C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416308 | ||||||
chr1:24416496
|
T | C | 126 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(123): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-258+592T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416496 | ||||||
chr1:24416532
|
C | G | 2 | a0001c0002t0002g0143a0001c0002t0003g0144 | 2 | NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-258+628C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416532 | ||||||
chr1:24416609
|
A | G | 1 | a0001c0001t0034g0328 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-258+705A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416609 | ||||||
chr1:24416616
|
C | T | 3 | a0001c0001t0001g0326a0001c0001t0013g0327a0001c0001t0034g0328 | 3 | HG00639.hp1 HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-258+712C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416616 | ||||||
chr1:24416724
|
G | A | 5 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0035g0145others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-258+820G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416724 | ||||||
chr1:24416733
|
T | G | 10 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0150others(7): Show | 15 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-258+829T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416733 | ||||||
chr1:24416824
|
A | G | 4 | a0001c0001t0030g0139a0001c0001t0030g0142a0001c0001t0064g0140others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-258+920A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24416824 | ||||||
chr1:24417003
|
G | A | 21 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0002g0171others(18): Show | 24 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-258+1099G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417003 | ||||||
chr1:24417090
|
C | T | 1 | a0001c0001t0014g0325 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-258+1186C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417090 | ||||||
chr1:24417113
|
C | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(23): Show | 29 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-258+1209C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417113 | ||||||
chr1:24417142
|
A | G | 1 | a0002c0007t0029g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-258+1238A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417142 | ||||||
chr1:24417272
|
G | C | 7 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0022g0031others(4): Show | 7 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-258+1368G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417272 | ||||||
chr1:24417293
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(68): Show | 83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-258+1389C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417293 | ||||||
chr1:24417389
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(71): Show | 86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-258+1485C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417389 | ||||||
chr1:24417941
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18967.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-257-1350A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417941 | ||||||
chr1:24417959
|
AAAAT | A | 4 | a0001c0001t0030g0139a0001c0001t0030g0142a0001c0001t0064g0140others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-257-1325_-257-132 others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 24417959 | |||||
chr1:24417968
|
A | G | 7 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-257-1323A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24417968 | ||||||
chr1:24418111
|
G | A | 2 | a0001c0001t0011g0176a0001c0001t0052g0175 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-257-1180G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418111 | ||||||
chr1:24418502
|
G | A | 2 | a0001c0001t0011g0176a0001c0001t0052g0175 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-257-789G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418502 | ||||||
chr1:24418580
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(276): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.-257-711T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418580 | ||||||
chr1:24418622
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(258): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.-257-669T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418622 | ||||||
chr1:24418672
|
T | A | 1 | a0001c0001t0001g0265 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-257-619T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418672 | ||||||
chr1:24418709
|
C | A | 1 | a0001c0001t0008g0266 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-257-582C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418709 | ||||||
chr1:24418920
|
G | GT | 10 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0002g0252others(7): Show | 10 | HG00673.hp1 HG02056.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.-257-355dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 24418920 | |||||
chr1:24418920
|
GT | G | 110 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(107): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-257-355delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 24418920 | |||||
chr1:24418941
|
C | T | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-257-350C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418941 | ||||||
chr1:24418948
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-257-343A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24418948 | ||||||
chr1:24419006
|
G | C | 1 | a0001c0002t0003g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-257-285G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419006 | ||||||
chr1:24419096
|
G | A | 2 | a0001c0001t0020g0157a0001c0001t0020g0158 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-257-195G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419096 | ||||||
chr1:24419125
|
G | A | 153 | a0001c0001t0001g0029a0001c0001t0001g0070a0001c0001t0001g0111others(150): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.-257-166G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419125 | ||||||
chr1:24419214
|
T | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(71): Show | 86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-257-77T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 1/11 | chr1 | 24419214 | ||||||
chr1:24419715
|
C | T | 128 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(125): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.93+75C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24419715 | ||||||
chr1:24419943
|
G | A | 21 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0002g0171others(18): Show | 24 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.93+303G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24419943 | ||||||
chr1:24420086
|
G | GA | 26 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0267others(23): Show | 29 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+462dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24420086 | |||||
chr1:24420086
|
G | GAA | 6 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028others(3): Show | 6 | HG01099.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+461_93+462dupAA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24420086 | |||||
chr1:24420087
|
A | G | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+447A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420087 | ||||||
chr1:24420384
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.93+744C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420384 | ||||||
chr1:24420520
|
T | C | 1 | a0001c0001t0014g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.93+880T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420520 | ||||||
chr1:24420594
|
T | G | 2 | a0001c0001t0007g0018a0001c0001t0059g0018 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.93+954T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420594 | ||||||
chr1:24420672
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.93+1032T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420672 | ||||||
chr1:24420695
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(70): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+1055G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420695 | ||||||
chr1:24420738
|
C | G | 24 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(21): Show | 27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+1098C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420738 | ||||||
chr1:24420778
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.93+1138G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420778 | ||||||
chr1:24420977
|
A | G | 24 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(21): Show | 27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+1337A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24420977 | ||||||
chr1:24421067
|
C | G | 14 | a0001c0001t0002g0035a0001c0001t0002g0256a0001c0001t0004g0006others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+1427C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421067 | ||||||
chr1:24421102
|
G | C | 4 | a0001c0001t0030g0139a0001c0001t0030g0142a0001c0001t0064g0140others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1462G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421102 | ||||||
chr1:24421134
|
C | T | 121 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.93+1494C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421134 | ||||||
chr1:24421163
|
A | G | 13 | a0001c0001t0001g0326a0001c0001t0004g0003a0001c0001t0004g0005others(10): Show | 18 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+1523A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421163 | ||||||
chr1:24421192
|
C | T | 135 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.93+1552C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421192 | ||||||
chr1:24421281
|
G | A | 1 | a0001c0001t0040g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.93+1641G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421281 | ||||||
chr1:24421351
|
C | CA | 7 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0022g0031others(4): Show | 7 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+1720dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24421351 | |||||
chr1:24421353
|
A | C | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.93+1713A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421353 | ||||||
chr1:24421393
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.93+1753G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421393 | ||||||
chr1:24421820
|
G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(21): Show | 27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+2180G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421820 | ||||||
chr1:24421847
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0002g0198a0001c0001t0004g0199 | 3 | HG00558.hp1 HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.93+2207T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421847 | ||||||
chr1:24421979
|
G | A | 2 | a0001c0001t0020g0160a0001c0001t0032g0159 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.93+2339G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24421979 | ||||||
chr1:24422090
|
T | C | 1 | a0001c0001t0055g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93+2450T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422090 | ||||||
chr1:24422094
|
A | C | 1 | a0001c0001t0002g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+2454A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422094 | ||||||
chr1:24422149
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93+2509C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422149 | ||||||
chr1:24422210
|
C | T | 2 | a0001c0002t0003g0124a0001c0002t0003g0125 | 2 | HG02015.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.93+2570C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422210 | ||||||
chr1:24422284
|
G | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(21): Show | 27 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.93+2644G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422284 | ||||||
chr1:24422339
|
A | G | 117 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.93+2699A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422339 | ||||||
chr1:24422520
|
C | T | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+2880C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422520 | ||||||
chr1:24422589
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(70): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+2949C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422589 | ||||||
chr1:24422590
|
G | A | 1 | a0001c0002t0006g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93+2950G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422590 | ||||||
chr1:24422837
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(276): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.93+3197A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422837 | ||||||
chr1:24422887
|
A | G | 135 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.93+3247A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24422887 | ||||||
chr1:24423216
|
G | A | 121 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.93+3576G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423216 | ||||||
chr1:24423406
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.93+3766C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423406 | ||||||
chr1:24423445
|
G | A | 18 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(15): Show | 19 | HG00733.hp1 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+3805G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423445 | ||||||
chr1:24423456
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(244): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.93+3816A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423456 | ||||||
chr1:24423463
|
C | G | 2 | a0001c0002t0001g0148a0001c0002t0045g0149 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.93+3823C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423463 | ||||||
chr1:24423552
|
C | T | 1 | a0001c0002t0001g0025 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.93+3912C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423552 | ||||||
chr1:24423572
|
G | A | 3 | a0001c0001t0012g0041a0001c0002t0001g0040a0001c0002t0058g0039 | 3 | HG01358.hp1 NA18952.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.93+3932G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423572 | ||||||
chr1:24423579
|
G | A | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.93+3939G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423579 | ||||||
chr1:24423585
|
G | A | 1 | a0001c0001t0009g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.93+3945G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423585 | ||||||
chr1:24423641
|
C | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(274): Show | 303 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.93+4001C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423641 | ||||||
chr1:24423864
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.93+4224C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423864 | ||||||
chr1:24423986
|
A | G | 10 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0150others(7): Show | 15 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.93+4346A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24423986 | ||||||
chr1:24424103
|
T | C | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+4463T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424103 | ||||||
chr1:24424356
|
T | C | 2 | a0001c0001t0001g0326a0001c0001t0034g0328 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.93+4716T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424356 | ||||||
chr1:24424388
|
T | C | 12 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(9): Show | 13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.93+4748T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424388 | ||||||
chr1:24424484
|
C | T | 2 | a0001c0001t0011g0176a0001c0001t0052g0175 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.93+4844C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424484 | ||||||
chr1:24424502
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0002g0271 | 2 | HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.93+4862G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424502 | ||||||
chr1:24424512
|
G | A | 1 | a0001c0001t0042g0319 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.93+4872G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424512 | ||||||
chr1:24424707
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(276): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.93+5067T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24424707 | ||||||
chr1:24425005
|
A | G | 3 | a0001c0002t0002g0123a0001c0002t0002g0143a0001c0002t0003g0144 | 3 | NA19062.hp1 NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.93+5365A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425005 | ||||||
chr1:24425164
|
A | G | 1 | a0001c0001t0004g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.93+5524A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425164 | ||||||
chr1:24425202
|
G | C | 1 | a0001c0001t0003g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.93+5562G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425202 | ||||||
chr1:24425283
|
T | C | 117 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.93+5643T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425283 | ||||||
chr1:24425319
|
AT | A | 135 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.93+5687delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24425319 | |||||
chr1:24425387
|
T | C | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | NA18980.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.93+5747T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425387 | ||||||
chr1:24425430
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(258): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.93+5790A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425430 | ||||||
chr1:24425497
|
C | T | 2 | a0001c0001t0011g0176a0001c0001t0052g0175 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.93+5857C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425497 | ||||||
chr1:24425527
|
G | A | 5 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0035g0145others(2): Show | 5 | HG01106.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+5887G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425527 | ||||||
chr1:24425544
|
A | G | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0118others(2): Show | 5 | HG02027.hp2 NA18943.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+5904A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425544 | ||||||
chr1:24425829
|
C | G | 9 | a0001c0001t0001g0326a0001c0001t0002g0256a0001c0001t0004g0006others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+6189C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24425829 | ||||||
chr1:24426083
|
C | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(282): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.93+6443C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426083 | ||||||
chr1:24426092
|
C | T | 2 | a0001c0001t0017g0263a0001c0001t0022g0264 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.93+6452C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426092 | ||||||
chr1:24426227
|
G | A | 4 | a0001c0001t0007g0185a0001c0001t0011g0183a0001c0001t0011g0186others(1): Show | 4 | HG00733.hp1 HG02080.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+6587G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426227 | ||||||
chr1:24426240
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(70): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+6600G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426240 | ||||||
chr1:24426270
|
C | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0045 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.93+6630C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426270 | ||||||
chr1:24426294
|
CT | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(71): Show | 86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.93+6667delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24426294 | |||||
chr1:24426376
|
C | A | 117 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.93+6736C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426376 | ||||||
chr1:24426453
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(282): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.93+6813T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426453 | ||||||
chr1:24426674
|
G | A | 117 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.93+7034G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426674 | ||||||
chr1:24426808
|
G | A | 1 | a0001c0001t0007g0019 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.93+7168G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426808 | ||||||
chr1:24426820
|
G | A | 135 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.93+7180G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426820 | ||||||
chr1:24426839
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.93+7199C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426839 | ||||||
chr1:24426860
|
T | C | 1 | a0001c0001t0050g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.93+7220T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426860 | ||||||
chr1:24426999
|
G | A | 1 | a0001c0002t0001g0272 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.93+7359G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24426999 | ||||||
chr1:24427271
|
G | T | 1 | a0001c0001t0013g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93+7631G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427271 | ||||||
chr1:24427708
|
A | G | 1 | a0001c0002t0001g0043 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.93+8068A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427708 | ||||||
chr1:24427764
|
G | T | 2 | a0001c0001t0005g0248a0001c0001t0005g0249 | 2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.93+8124G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427764 | ||||||
chr1:24427778
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(70): Show | 85 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.93+8138A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427778 | ||||||
chr1:24427916
|
T | A | 121 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.93+8276T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427916 | ||||||
chr1:24427936
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(244): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.93+8296G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427936 | ||||||
chr1:24427979
|
C | G | 2 | a0001c0001t0001g0326a0001c0001t0034g0328 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.93+8339C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427979 | ||||||
chr1:24427993
|
C | T | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8353C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24427993 | ||||||
chr1:24428030
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(155): Show | 181 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.93+8390A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428030 | ||||||
chr1:24428104
|
A | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0315a0001c0001t0002g0271 | 3 | HG00735.hp1 HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.93+8464A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428104 | ||||||
chr1:24428197
|
G | A | 1 | a0001c0001t0038g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93+8557G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428197 | ||||||
chr1:24428216
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0313 | 3 | HG02129.hp1 NA18612.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.93+8576A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428216 | ||||||
chr1:24428237
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.93+8597C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428237 | ||||||
chr1:24428254
|
A | AAAAAGAG others(10): Show |
1 | a0001c0002t0015g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.93+8615_93+8616ins others(17): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428254 | |||||
chr1:24428254
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0002g0261 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.93+8614_93+8615ins others(11): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428254 | ||||||
chr1:24428258
|
A | AAG | 16 | a0001c0001t0002g0057a0001c0001t0002g0215a0001c0001t0002g0216others(13): Show | 18 | HG00597.hp1 HG01070.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.93+8662_93+8663dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAG | 14 | a0001c0001t0001g0219a0001c0001t0002g0218a0001c0001t0002g0250others(11): Show | 14 | HG01952.hp2 HG02109.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+8660_93+8663dup others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAG | 15 | a0001c0001t0002g0251a0001c0001t0009g0222a0001c0001t0038g0201others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.93+8658_93+8663dup others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(1): Show |
21 | a0001c0001t0001g0070a0001c0001t0002g0198a0001c0001t0002g0225others(18): Show | 21 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.93+8656_93+8663dup others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(3): Show |
24 | a0001c0001t0001g0197a0001c0001t0002g0020a0001c0001t0002g0228others(21): Show | 26 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.93+8654_93+8663dup others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(5): Show |
18 | a0001c0001t0002g0237a0001c0001t0002g0239a0001c0001t0007g0185others(15): Show | 18 | HG00733.hp1 HG01069.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.93+8652_93+8663dup others(12): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(7): Show |
13 | a0001c0001t0002g0126a0001c0001t0002g0242a0001c0001t0008g0241others(10): Show | 13 | HG01099.hp2 HG01496.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+8650_93+8663dup others(14): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(9): Show |
14 | a0001c0001t0001g0121a0001c0001t0002g0243a0001c0001t0005g0249others(11): Show | 14 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+8648_93+8663dup others(16): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(11): Show |
9 | a0001c0001t0002g0021a0001c0001t0002g0205a0001c0001t0071g0021others(6): Show | 9 | HG02300.hp2 HG03579.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.93+8646_93+8663dup others(18): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(13): Show |
6 | a0001c0002t0001g0101a0001c0002t0001g0105a0001c0002t0003g0014others(3): Show | 7 | HG01257.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+8644_93+8663dup others(20): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(15): Show |
1 | a0001c0001t0011g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.93+8642_93+8663dup others(22): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(19): Show |
2 | a0001c0002t0003g0107a0001c0002t0006g0106 | 2 | NA19066.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.93+8638_93+8663dup others(26): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AAGAGAGA others(27): Show |
1 | a0001c0002t0061g0108 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.93+8630_93+8663dup others(34): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
A | AGAG | 3 | a0001c0001t0004g0258a0001c0002t0003g0109a0001c0002t0003g0110 | 3 | HG00438.hp1 HG01071.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.93+8618_93+8619ins others(3): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(2): Show |
5 | a0001c0001t0001g0111a0001c0001t0002g0177a0001c0001t0003g0202others(2): Show | 5 | HG01346.hp1 HG02132.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+8618_93+8619ins others(9): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0069g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(11): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(6): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0002t0001g0112others(1): Show | 4 | HG00280.hp2 HG03491.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+8618_93+8619ins others(13): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(8): Show |
1 | a0001c0002t0001g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(15): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(10): Show |
1 | a0001c0008t0003g0312 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(17): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(12): Show |
1 | a0001c0002t0018g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(19): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | AGAGAGAG others(22): Show |
1 | a0001c0001t0011g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.93+8618_93+8619ins others(29): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
A | G | 3 | a0001c0001t0002g0261a0001c0002t0003g0117a0001c0002t0015g0046 | 3 | HG04228.hp2 NA18968.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.93+8618A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428258 | ||||||
chr1:24428258
|
AAG | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0207a0001c0001t0002g0252others(13): Show | 22 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+8662_93+8663del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAG | A | 4 | a0001c0001t0004g0156a0001c0001t0007g0188a0001c0002t0001g0148others(1): Show | 4 | HG02818.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+8660_93+8663del others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAG | A | 9 | a0001c0001t0002g0004a0001c0001t0002g0035a0001c0001t0004g0003others(6): Show | 14 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.93+8658_93+8663del others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAGA others(1): Show |
A | 24 | a0001c0001t0001g0306a0001c0001t0001g0309a0001c0001t0001g0311others(21): Show | 26 | HG00639.hp1 HG00673.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.93+8656_93+8663del others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAGA others(3): Show |
A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(80): Show | 98 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.93+8654_93+8663del others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAGA others(5): Show |
A | 1 | a0001c0001t0005g0274 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.93+8652_93+8663del others(12): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAGA others(7): Show |
A | 4 | a0001c0001t0001g0314a0001c0001t0002g0206a0001c0001t0014g0325others(1): Show | 4 | HG01981.hp2 NA18970.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+8650_93+8663del others(14): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAGA others(9): Show |
A | 1 | a0001c0001t0021g0329 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.93+8648_93+8663del others(16): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428258
|
AAGAGAGA others(13): Show |
A | 1 | a0001c0001t0001g0273 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.93+8644_93+8663del others(20): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428258 | |||||
chr1:24428294
|
GAGAGAGA others(3): Show |
G | 2 | a0001c0001t0049g0259a0001c0002t0036g0047 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.93+8656_93+8665del others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428294 | |||||
chr1:24428299
|
A | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(23): Show | 29 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+8659A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428299 | ||||||
chr1:24428300
|
G | GAGAGAGA others(3): Show |
1 | a0001c0002t0003g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.93+8663_93+8664ins others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428300 | |||||
chr1:24428302
|
GAC | G | 3 | a0001c0002t0001g0052a0001c0002t0003g0051a0001c0002t0003g0124 | 3 | HG01975.hp1 HG02015.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.93+8665_93+8666del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24428302 | |||||
chr1:24428304
|
C | G | 112 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.93+8664C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428304 | ||||||
chr1:24428307
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8667C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428307 | ||||||
chr1:24428312
|
C | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0272a0001c0002t0001g0275 | 4 | NA18944.hp2 NA18999.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+8672C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428312 | ||||||
chr1:24428312
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8672C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428312 | ||||||
chr1:24428313
|
C | A | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8673C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428313 | ||||||
chr1:24428314
|
T | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8674T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428314 | ||||||
chr1:24428315
|
T | A | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8675T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428315 | ||||||
chr1:24428316
|
T | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8676T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428316 | ||||||
chr1:24428317
|
C | A | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8677C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428317 | ||||||
chr1:24428318
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8678C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428318 | ||||||
chr1:24428319
|
C | A | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8679C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428319 | ||||||
chr1:24428320
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8680C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428320 | ||||||
chr1:24428322
|
A | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8682A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428322 | ||||||
chr1:24428325
|
C | A | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8685C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428325 | ||||||
chr1:24428326
|
C | G | 1 | a0001c0001t0011g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.93+8686C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428326 | ||||||
chr1:24428429
|
A | C | 39 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(36): Show | 43 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.93+8789A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428429 | ||||||
chr1:24428502
|
C | T | 1 | a0001c0002t0002g0082 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.93+8862C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428502 | ||||||
chr1:24428513
|
G | A | 32 | a0001c0001t0006g0146a0001c0001t0007g0018a0001c0001t0007g0019others(29): Show | 34 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.93+8873G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428513 | ||||||
chr1:24428518
|
G | A | 119 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.93+8878G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428518 | ||||||
chr1:24428575
|
A | G | 1 | a0001c0002t0003g0318 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.93+8935A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428575 | ||||||
chr1:24428714
|
G | A | 119 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.93+9074G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428714 | ||||||
chr1:24428791
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.93+9151G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428791 | ||||||
chr1:24428796
|
C | A | 3 | a0001c0001t0017g0263a0001c0001t0022g0264a0001c0002t0012g0262 | 3 | HG01106.hp2 HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.93+9156C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428796 | ||||||
chr1:24428948
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(141): Show | 166 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.93+9308G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428948 | ||||||
chr1:24428994
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.93+9354C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24428994 | ||||||
chr1:24429043
|
G | A | 1 | a0001c0001t0038g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93+9403G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429043 | ||||||
chr1:24429044
|
C | T | 15 | a0001c0001t0001g0326a0001c0001t0004g0003a0001c0001t0004g0005others(12): Show | 21 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.93+9404C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429044 | ||||||
chr1:24429214
|
A | G | 1 | a0001c0001t0038g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.93+9574A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429214 | ||||||
chr1:24429354
|
C | CA | 344 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(341): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.93+9714_93+9715ins others(1): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429354 | ||||||
chr1:24429503
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(154): Show | 180 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.93+9863C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429503 | ||||||
chr1:24429724
|
T | C | 2 | a0001c0002t0003g0069a0001c0002t0003g0083 | 2 | HG00323.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.93+10084T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429724 | ||||||
chr1:24429840
|
C | G | 1 | a0001c0001t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.93+10200C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429840 | ||||||
chr1:24429942
|
G | C | 1 | a0001c0001t0007g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.94-10230G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429942 | ||||||
chr1:24429952
|
T | C | 7 | a0001c0001t0005g0213a0001c0001t0005g0226a0001c0004t0005g0217others(4): Show | 7 | HG00609.hp1 HG02074.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-10220T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429952 | ||||||
chr1:24429984
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-10188G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24429984 | ||||||
chr1:24430214
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-9958G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430214 | ||||||
chr1:24430235
|
CT | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(147): Show | 173 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.94-9923delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24430235 | |||||
chr1:24430235
|
CTT | C | 8 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0022g0031others(5): Show | 8 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-9924_94-9923del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24430235 | |||||
chr1:24430290
|
T | TGGAGTGC others(1): Show |
119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(116): Show | 139 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.94-9873_94-9866dup others(8): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24430290 | |||||
chr1:24430313
|
C | T | 45 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(42): Show | 53 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-9859C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430313 | ||||||
chr1:24430314
|
G | A | 1 | a0001c0001t0034g0328 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.94-9858G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430314 | ||||||
chr1:24430377
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9795A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430377 | ||||||
chr1:24430450
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9722G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430450 | ||||||
chr1:24430534
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(277): Show | 306 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.94-9638A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430534 | ||||||
chr1:24430540
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.94-9632G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430540 | ||||||
chr1:24430639
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9533C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430639 | ||||||
chr1:24430701
|
T | C | 1 | a0001c0001t0050g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-9471T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430701 | ||||||
chr1:24430718
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(68): Show | 83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.94-9454A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430718 | ||||||
chr1:24430729
|
G | A | 12 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(9): Show | 18 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.94-9443G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430729 | ||||||
chr1:24430851
|
C | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-9321C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430851 | ||||||
chr1:24430859
|
G | A | 7 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-9313G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24430859 | ||||||
chr1:24431277
|
A | G | 4 | a0001c0001t0030g0139a0001c0001t0030g0142a0001c0001t0064g0140others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-8895A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431277 | ||||||
chr1:24431316
|
C | T | 19 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0002g0171others(16): Show | 21 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.94-8856C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431316 | ||||||
chr1:24431504
|
A | G | 3 | a0001c0001t0001g0305a0001c0001t0001g0314a0001c0001t0012g0310 | 3 | HG00733.hp2 HG01981.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.94-8668A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431504 | ||||||
chr1:24431803
|
AC | A | 4 | a0001c0001t0004g0006a0001c0001t0004g0257a0001c0001t0004g0258others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-8364delC | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24431803 | |||||
chr1:24431813
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94-8359C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431813 | ||||||
chr1:24431844
|
C | T | 1 | a0001c0003t0003g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.94-8328C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24431844 | ||||||
chr1:24432001
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0020g0034 | 2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.94-8171C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432001 | ||||||
chr1:24432002
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94-8170G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432002 | ||||||
chr1:24432038
|
C | T | 14 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0017g0026others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-8134C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432038 | ||||||
chr1:24432114
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-8058C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432114 | ||||||
chr1:24432117
|
A | G | 30 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(27): Show | 37 | HG00733.hp1 HG01069.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-8055A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432117 | ||||||
chr1:24432158
|
T | C | 4 | a0001c0002t0001g0084a0001c0002t0001g0089a0001c0002t0001g0101others(1): Show | 4 | HG03490.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-8014T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432158 | ||||||
chr1:24432193
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(140): Show | 165 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.94-7979A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432193 | ||||||
chr1:24432244
|
C | T | 2 | a0001c0001t0011g0176a0001c0001t0052g0175 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94-7928C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432244 | ||||||
chr1:24432449
|
T | C | 1 | a0001c0001t0011g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-7723T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432449 | ||||||
chr1:24432535
|
C | T | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-7637C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432535 | ||||||
chr1:24432569
|
T | C | 118 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.94-7603T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432569 | ||||||
chr1:24432723
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0002g0304 | 2 | HG01123.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.94-7449G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432723 | ||||||
chr1:24432849
|
G | C | 3 | a0001c0002t0002g0123a0001c0002t0002g0143a0001c0002t0003g0144 | 3 | NA19062.hp1 NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.94-7323G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432849 | ||||||
chr1:24432913
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(139): Show | 164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-7259G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432913 | ||||||
chr1:24432919
|
A | G | 2 | a0001c0001t0011g0176a0001c0001t0052g0175 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94-7253A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432919 | ||||||
chr1:24432939
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(139): Show | 164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-7233G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432939 | ||||||
chr1:24432985
|
A | G | 14 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0017g0026others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-7187A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24432985 | ||||||
chr1:24433124
|
C | T | 1 | a0001c0001t0023g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.94-7048C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433124 | ||||||
chr1:24433125
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.94-7047G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433125 | ||||||
chr1:24433195
|
G | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(115): Show | 138 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.94-6977G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433195 | ||||||
chr1:24433440
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(67): Show | 82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.94-6732C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433440 | ||||||
chr1:24433629
|
G | A | 7 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0022g0031others(4): Show | 7 | HG02145.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-6543G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433629 | ||||||
chr1:24433633
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(139): Show | 164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-6539C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433633 | ||||||
chr1:24433708
|
T | C | 1 | a0001c0001t0060g0214 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.94-6464T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433708 | ||||||
chr1:24433759
|
A | G | 12 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(9): Show | 18 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.94-6413A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433759 | ||||||
chr1:24433809
|
G | T | 12 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(9): Show | 13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.94-6363G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433809 | ||||||
chr1:24433823
|
TG | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(139): Show | 164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-6346delG | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24433823 | |||||
chr1:24433826
|
G | A | 6 | a0001c0003t0001g0133a0001c0003t0003g0038a0001c0003t0003g0075others(3): Show | 6 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-6346G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433826 | ||||||
chr1:24433927
|
C | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(139): Show | 164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-6245C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433927 | ||||||
chr1:24433940
|
A | C | 1 | a0001c0002t0003g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-6232A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24433940 | ||||||
chr1:24434001
|
T | C | 1 | a0001c0001t0007g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94-6171T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434001 | ||||||
chr1:24434164
|
T | C | 45 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(42): Show | 53 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-6008T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434164 | ||||||
chr1:24434309
|
A | G | 14 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0017g0026others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-5863A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434309 | ||||||
chr1:24434489
|
G | A | 2 | a0001c0002t0006g0091a0001c0002t0006g0102 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.94-5683G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434489 | ||||||
chr1:24434553
|
T | C | 1 | a0001c0001t0029g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94-5619T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434553 | ||||||
chr1:24434812
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(276): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.94-5360C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434812 | ||||||
chr1:24434853
|
T | G | 1 | a0001c0001t0002g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94-5319T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434853 | ||||||
chr1:24434901
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(139): Show | 164 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.94-5271A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24434901 | ||||||
chr1:24435345
|
A | G | 1 | a0001c0010t0003g0227 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.94-4827A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435345 | ||||||
chr1:24435500
|
C | A | 3 | a0001c0001t0001g0197a0001c0001t0002g0198a0001c0001t0004g0199 | 3 | HG00558.hp1 HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.94-4672C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435500 | ||||||
chr1:24435572
|
C | T | 1 | a0001c0002t0003g0100 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.94-4600C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435572 | ||||||
chr1:24435573
|
G | A | 1 | a0001c0002t0003g0100 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.94-4599G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435573 | ||||||
chr1:24435574
|
C | T | 1 | a0001c0002t0003g0100 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.94-4598C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435574 | ||||||
chr1:24435579
|
A | G | 24 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(21): Show | 26 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.94-4593A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435579 | ||||||
chr1:24435605
|
C | T | 1 | a0001c0002t0002g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94-4567C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435605 | ||||||
chr1:24435660
|
A | G | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-4512A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435660 | ||||||
chr1:24435769
|
G | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0045 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.94-4403G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435769 | ||||||
chr1:24435896
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94-4276G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435896 | ||||||
chr1:24435970
|
G | A | 8 | a0001c0001t0017g0026a0001c0001t0021g0329a0001c0001t0021g0330others(5): Show | 9 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-4202G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24435970 | ||||||
chr1:24436041
|
A | G | 1 | a0001c0002t0001g0025 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.94-4131A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436041 | ||||||
chr1:24436068
|
G | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(275): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.94-4104G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436068 | ||||||
chr1:24436086
|
C | T | 14 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0017g0026others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-4086C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436086 | ||||||
chr1:24436149
|
G | A | 23 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(20): Show | 25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.94-4023G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436149 | ||||||
chr1:24436221
|
G | A | 1 | a0001c0001t0032g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94-3951G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436221 | ||||||
chr1:24436251
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(138): Show | 163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3921C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436251 | ||||||
chr1:24436252
|
A | T | 2 | a0001c0001t0024g0194a0001c0001t0024g0195 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.94-3920A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436252 | ||||||
chr1:24436309
|
T | A | 1 | a0001c0001t0014g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.94-3863T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436309 | ||||||
chr1:24436359
|
A | G | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.94-3813A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436359 | ||||||
chr1:24436444
|
A | G | 13 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(10): Show | 14 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.94-3728A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436444 | ||||||
chr1:24436497
|
T | C | 1 | a0001c0002t0003g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.94-3675T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436497 | ||||||
chr1:24436510
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(137): Show | 162 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.94-3662C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436510 | ||||||
chr1:24436522
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94-3650C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436522 | ||||||
chr1:24436572
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(138): Show | 163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3600T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436572 | ||||||
chr1:24436640
|
C | G | 4 | a0001c0001t0030g0139a0001c0001t0030g0142a0001c0001t0064g0140others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3532C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436640 | ||||||
chr1:24436645
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(67): Show | 82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.94-3527C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436645 | ||||||
chr1:24436653
|
T | TAA | 45 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(42): Show | 53 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.94-3518_94-3517dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24436653 | |||||
chr1:24436679
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(275): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.94-3493G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436679 | ||||||
chr1:24436765
|
C | T | 4 | a0001c0001t0030g0139a0001c0001t0030g0142a0001c0001t0064g0140others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3407C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436765 | ||||||
chr1:24436791
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(138): Show | 163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3381G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436791 | ||||||
chr1:24436795
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(138): Show | 163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3377A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436795 | ||||||
chr1:24436841
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(138): Show | 163 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.94-3331A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436841 | ||||||
chr1:24436857
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.94-3315G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24436857 | ||||||
chr1:24437023
|
G | T | 1 | a0002c0007t0029g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-3149G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437023 | ||||||
chr1:24437061
|
A | C | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94-3111A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437061 | ||||||
chr1:24437120
|
C | T | 107 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0114others(104): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.94-3052C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437120 | ||||||
chr1:24437125
|
G | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0045 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.94-3047G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437125 | ||||||
chr1:24437176
|
C | T | 9 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028others(6): Show | 9 | HG01099.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-2996C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437176 | ||||||
chr1:24437201
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94-2971G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437201 | ||||||
chr1:24437304
|
T | G | 2 | a0001c0001t0001g0306a0001c0001t0005g0274 | 2 | NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.94-2868T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437304 | ||||||
chr1:24437361
|
A | G | 1 | a0001c0001t0008g0302 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.94-2811A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437361 | ||||||
chr1:24437447
|
G | C | 1 | a0001c0001t0002g0252 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.94-2725G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437447 | ||||||
chr1:24437580
|
A | AAGGTCTG others(8): Show |
3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94-2575_94-2561dup others(15): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24437580 | |||||
chr1:24437802
|
T | G | 2 | a0001c0001t0006g0146a0001c0001t0035g0145 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.94-2370T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437802 | ||||||
chr1:24437807
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94-2365G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437807 | ||||||
chr1:24437841
|
G | A | 1 | a0001c0002t0006g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.94-2331G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24437841 | ||||||
chr1:24438199
|
C | T | 135 | a0001c0001t0001g0114a0001c0001t0002g0057a0001c0001t0002g0126others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.94-1973C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438199 | ||||||
chr1:24438211
|
G | A | 1 | a0001c0001t0031g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94-1961G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438211 | ||||||
chr1:24438229
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0016g0167a0001c0001t0047g0165others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-1943G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438229 | ||||||
chr1:24438252
|
T | C | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.94-1920T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438252 | ||||||
chr1:24438254
|
G | A | 2 | a0001c0001t0002g0237a0001c0001t0056g0245 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.94-1918G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438254 | ||||||
chr1:24438255
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-1917G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438255 | ||||||
chr1:24438264
|
G | A | 134 | a0001c0001t0001g0114a0001c0001t0002g0057a0001c0001t0002g0126others(131): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.94-1908G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438264 | ||||||
chr1:24438350
|
G | GT | 5 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(2): Show | 5 | HG01069.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1821dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24438350 | |||||
chr1:24438367
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94-1805C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438367 | ||||||
chr1:24438425
|
A | G | 123 | a0001c0001t0001g0114a0001c0001t0002g0057a0001c0001t0002g0126others(120): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.94-1747A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438425 | ||||||
chr1:24438436
|
A | T | 1 | a0001c0001t0037g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.94-1736A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438436 | ||||||
chr1:24438473
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0004g0027others(3): Show | 6 | HG00639.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-1699C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438473 | ||||||
chr1:24438475
|
G | A | 3 | a0001c0001t0001g0326a0001c0001t0013g0327a0001c0001t0034g0328 | 3 | HG00639.hp1 HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.94-1697G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438475 | ||||||
chr1:24438533
|
G | A | 1 | a0001c0001t0032g0159 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.94-1639G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438533 | ||||||
chr1:24438623
|
G | A | 23 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0002g0035others(20): Show | 25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.94-1549G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438623 | ||||||
chr1:24438813
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94-1359A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438813 | ||||||
chr1:24438888
|
TA | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(203): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.94-1281delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24438888 | |||||
chr1:24438923
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.94-1249T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24438923 | ||||||
chr1:24439032
|
G | A | 121 | a0001c0001t0001g0114a0001c0001t0002g0057a0001c0001t0002g0126others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.94-1140G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439032 | ||||||
chr1:24439047
|
G | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(203): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.94-1125G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439047 | ||||||
chr1:24439217
|
G | A | 7 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-955G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439217 | ||||||
chr1:24439249
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.94-923C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439249 | ||||||
chr1:24439390
|
A | G | 1 | a0001c0001t0020g0158 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.94-782A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439390 | ||||||
chr1:24439624
|
AAT | A | 8 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0021g0329others(5): Show | 8 | HG01106.hp1 HG01175.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.94-543_94-542delAT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24439624 | |||||
chr1:24439693
|
G | A | 1 | a0001c0001t0007g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.94-479G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439693 | ||||||
chr1:24439741
|
G | T | 1 | a0001c0001t0020g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.94-431G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439741 | ||||||
chr1:24439863
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-309T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | chr1 | 24439863 | ||||||
chr1:24440009
|
C | CT | 3 | a0001c0001t0001g0029a0001c0001t0004g0027a0001c0001t0004g0028 | 3 | HG02257.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.94-161dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 24440009 | |||||
chr1:24440296
|
G | A | 5 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(2): Show | 5 | HG01069.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+56G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440296 | ||||||
chr1:24440347
|
A | C | 1 | a0001c0001t0008g0266 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.162+107A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440347 | ||||||
chr1:24440431
|
G | A | 1 | a0001c0001t0011g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+191G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440431 | ||||||
chr1:24440500
|
C | G | 3 | a0001c0001t0001g0326a0001c0001t0013g0327a0001c0001t0034g0328 | 3 | HG00639.hp1 HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.162+260C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440500 | ||||||
chr1:24440715
|
C | G | 37 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(34): Show | 45 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.162+475C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440715 | ||||||
chr1:24440758
|
G | C | 3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.162+518G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440758 | ||||||
chr1:24440828
|
G | A | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.162+588G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440828 | ||||||
chr1:24440884
|
A | G | 1 | a0001c0001t0060g0214 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.162+644A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440884 | ||||||
chr1:24440936
|
C | T | 123 | a0001c0001t0001g0114a0001c0001t0002g0057a0001c0001t0002g0126others(120): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.162+696C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440936 | ||||||
chr1:24440947
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.162+707C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24440947 | ||||||
chr1:24441005
|
G | A | 4 | a0001c0001t0007g0182a0001c0001t0007g0188a0001c0001t0007g0190others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+765G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441005 | ||||||
chr1:24441128
|
C | T | 23 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0002g0035others(20): Show | 25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+888C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441128 | ||||||
chr1:24441255
|
C | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(80): Show | 95 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.163-800C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441255 | ||||||
chr1:24441284
|
T | A | 2 | a0001c0002t0006g0091a0001c0002t0006g0102 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.163-771T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441284 | ||||||
chr1:24441298
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.163-757C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441298 | ||||||
chr1:24441472
|
C | T | 1 | a0001c0001t0038g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163-583C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441472 | ||||||
chr1:24441473
|
C | T | 11 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(8): Show | 12 | HG00733.hp1 HG01243.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-582C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441473 | ||||||
chr1:24441610
|
C | T | 5 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(2): Show | 5 | HG01069.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-445C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441610 | ||||||
chr1:24441612
|
AAC | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0197others(6): Show | 11 | HG00544.hp2 HG00621.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-437_163-436del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 24441612 | |||||
chr1:24441670
|
G | A | 11 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0017g0026others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-385G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441670 | ||||||
chr1:24441979
|
G | A | 34 | a0001c0001t0001g0029a0001c0001t0001g0164a0001c0001t0001g0170others(31): Show | 36 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.163-76G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 3/11 | chr1 | 24441979 | ||||||
chr1:24442288
|
G | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(273): Show | 302 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.334+62G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442288 | ||||||
chr1:24442367
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.334+141C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442367 | ||||||
chr1:24442477
|
G | C | 12 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(9): Show | 13 | HG00733.hp1 HG01243.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.334+251G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442477 | ||||||
chr1:24442578
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02027.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.334+352G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442578 | ||||||
chr1:24442694
|
T | C | 7 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+468T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442694 | ||||||
chr1:24442743
|
G | C | 3 | a0001c0002t0006g0091a0001c0002t0006g0102a0001c0002t0006g0255 | 3 | HG02145.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.334+517G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442743 | ||||||
chr1:24442815
|
A | G | 2 | a0001c0001t0001g0324a0001c0001t0015g0298 | 2 | NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.334+589A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442815 | ||||||
chr1:24442844
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(274): Show | 303 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.334+618T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442844 | ||||||
chr1:24442926
|
C | T | 23 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0002g0035others(20): Show | 25 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.334+700C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24442926 | ||||||
chr1:24443269
|
T | C | 36 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(33): Show | 43 | HG00733.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.334+1043T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443269 | ||||||
chr1:24443439
|
T | C | 7 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+1213T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443439 | ||||||
chr1:24443531
|
C | T | 7 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+1305C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443531 | ||||||
chr1:24443545
|
A | T | 1 | a0001c0001t0013g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.334+1319A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443545 | ||||||
chr1:24443649
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(61): Show | 75 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.334+1423C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443649 | ||||||
chr1:24443663
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.334+1437C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443663 | ||||||
chr1:24443967
|
G | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(223): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.335-1218G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24443967 | ||||||
chr1:24444018
|
C | CT | 253 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(250): Show | 277 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.335-1155dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 24444018 | |||||
chr1:24444018
|
C | CTT | 14 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(11): Show | 16 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.335-1156_335-1155d others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 24444018 | |||||
chr1:24444063
|
A | G | 2 | a0001c0001t0030g0139a0001c0001t0030g0142 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.335-1122A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444063 | ||||||
chr1:24444104
|
G | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(223): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.335-1081G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444104 | ||||||
chr1:24444252
|
A | G | 2 | a0001c0001t0064g0140a0001c0001t0065g0141 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.335-933A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444252 | ||||||
chr1:24444341
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.335-844A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444341 | ||||||
chr1:24444370
|
GA | G | 3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.335-811delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 24444370 | |||||
chr1:24444406
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.335-779A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444406 | ||||||
chr1:24444409
|
G | T | 3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.335-776G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444409 | ||||||
chr1:24444703
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.335-482T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444703 | ||||||
chr1:24444944
|
T | C | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.335-241T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444944 | ||||||
chr1:24444951
|
C | T | 6 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.335-234C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24444951 | ||||||
chr1:24445116
|
C | T | 1 | a0001c0001t0005g0074 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.335-69C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 4/11 | chr1 | 24445116 | ||||||
chr1:24445302
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0034g0328 | 3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.394+58G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445302 | ||||||
chr1:24445440
|
C | T | 3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.394+196C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445440 | ||||||
chr1:24445493
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0034g0328 | 3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.394+249C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445493 | ||||||
chr1:24445719
|
C | G | 1 | a0001c0001t0031g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.394+475C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445719 | ||||||
chr1:24445776
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.394+532G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445776 | ||||||
chr1:24445975
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(272): Show | 301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.394+731T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24445975 | ||||||
chr1:24446069
|
C | CGT | 9 | a0001c0001t0001g0326a0001c0001t0002g0304a0001c0001t0013g0192others(6): Show | 9 | HG00639.hp2 HG01069.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+862_394+863dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446069
|
C | CT | 3 | a0001c0001t0020g0160a0001c0001t0022g0032a0001c0001t0032g0163 | 3 | HG02486.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.394+825_394+826ins others(1): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGT | 7 | a0001c0001t0001g0276a0001c0001t0002g0035a0001c0001t0020g0034others(4): Show | 7 | HG02145.hp1 HG02965.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(3): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGTGT | 6 | a0001c0001t0015g0296a0001c0001t0020g0157a0001c0001t0020g0158others(3): Show | 6 | HG00597.hp2 HG00741.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(5): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGTGTGT | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(55): Show | 70 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(7): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGTGTGT others(2): Show |
16 | a0001c0001t0001g0070a0001c0001t0001g0273a0001c0001t0001g0283others(13): Show | 18 | HG00673.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.394+825_394+826ins others(9): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGTGTGT others(4): Show |
2 | a0001c0001t0050g0162a0002c0007t0029g0174 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.394+825_394+826ins others(11): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGTGTGT others(6): Show |
2 | a0001c0001t0001g0282a0001c0001t0002g0256 | 2 | HG00423.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.394+825_394+826ins others(13): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
C | CTGTGTGT others(10): Show |
1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.394+825_394+826ins others(17): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446069 | ||||||
chr1:24446069
|
CGT | C | 65 | a0001c0001t0001g0029a0001c0001t0001g0219a0001c0001t0002g0002others(62): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.394+862_394+863del others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446069
|
CGTGT | C | 8 | a0001c0001t0002g0205a0001c0001t0009g0236a0001c0002t0001g0063others(5): Show | 8 | HG02300.hp1 HG03579.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.394+860_394+863del others(4): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446069
|
CGTGTGT | C | 118 | a0001c0001t0012g0041a0001c0001t0017g0026a0001c0002t0001g0009others(115): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.394+858_394+863del others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446069
|
CGTGTGTG others(13): Show |
C | 2 | a0001c0001t0030g0139a0001c0001t0030g0142 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.394+844_394+863del others(20): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446069
|
CGTGTGTG others(15): Show |
C | 36 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(33): Show | 43 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.394+842_394+863del others(22): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446069
|
CGTGTGTG others(17): Show |
C | 1 | a0001c0001t0007g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.394+840_394+863del others(24): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24446069 | |||||
chr1:24446196
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.394+952G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446196 | ||||||
chr1:24446204
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.394+960G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446204 | ||||||
chr1:24446210
|
T | C | 1 | a0001c0001t0004g0151 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.394+966T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446210 | ||||||
chr1:24446233
|
C | T | 1 | a0001c0002t0001g0025 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.394+989C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446233 | ||||||
chr1:24446373
|
A | G | 1 | a0001c0001t0002g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.394+1129A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446373 | ||||||
chr1:24446519
|
A | G | 21 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(18): Show | 23 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.394+1275A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446519 | ||||||
chr1:24446543
|
T | C | 39 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(36): Show | 46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.394+1299T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446543 | ||||||
chr1:24446546
|
A | G | 22 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(19): Show | 24 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.394+1302A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446546 | ||||||
chr1:24446572
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(340): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.394+1328T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446572 | ||||||
chr1:24446601
|
T | C | 128 | a0001c0001t0012g0041a0001c0001t0017g0026a0001c0002t0001g0009others(125): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.394+1357T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446601 | ||||||
chr1:24446613
|
T | A | 2 | a0001c0001t0030g0139a0001c0001t0030g0142 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.394+1369T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446613 | ||||||
chr1:24446638
|
G | A | 39 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(36): Show | 46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.394+1394G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446638 | ||||||
chr1:24446880
|
C | G | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.394+1636C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24446880 | ||||||
chr1:24447115
|
A | G | 2 | a0001c0001t0017g0263a0001c0001t0022g0264 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.394+1871A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447115 | ||||||
chr1:24447144
|
G | A | 27 | a0001c0001t0006g0146a0001c0001t0007g0018a0001c0001t0007g0019others(24): Show | 28 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.394+1900G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447144 | ||||||
chr1:24447222
|
C | T | 4 | a0001c0001t0002g0020a0001c0001t0002g0235a0001c0001t0002g0242others(1): Show | 5 | HG00140.hp2 HG00741.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+1978C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447222 | ||||||
chr1:24447286
|
A | G | 39 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(36): Show | 46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.394+2042A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447286 | ||||||
chr1:24447313
|
T | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(272): Show | 301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.394+2069T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447313 | ||||||
chr1:24447486
|
C | G | 1 | a0001c0001t0004g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395-1995C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447486 | ||||||
chr1:24447782
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395-1699G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447782 | ||||||
chr1:24447783
|
A | T | 1 | a0001c0001t0001g0299 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395-1698A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447783 | ||||||
chr1:24447798
|
A | C | 2 | a0001c0001t0022g0031a0001c0001t0022g0032 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.395-1683A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447798 | ||||||
chr1:24447986
|
G | T | 2 | a0001c0001t0006g0146a0001c0001t0035g0145 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.395-1495G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24447986 | ||||||
chr1:24448009
|
C | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.395-1472C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448009 | ||||||
chr1:24448284
|
G | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(222): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.395-1197G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448284 | ||||||
chr1:24448370
|
C | A | 1 | a0001c0001t0013g0327 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.395-1111C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448370 | ||||||
chr1:24448424
|
ATAGTAAT | A | 3 | a0001c0003t0001g0133a0001c0003t0003g0076a0001c0003t0003g0077 | 3 | HG00423.hp1 NA19000.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.395-1054_395-1048d others(9): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448424 | |||||
chr1:24448510
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(93): Show | 110 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.395-971C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448510 | ||||||
chr1:24448590
|
A | G | 1 | a0001c0002t0062g0062 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.395-891A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448590 | ||||||
chr1:24448604
|
A | G | 8 | a0001c0001t0002g0234a0001c0001t0009g0200a0001c0001t0009g0221others(5): Show | 8 | HG00099.hp1 HG01168.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-877A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24448604 | ||||||
chr1:24448673
|
C | CAAGAATG others(2903): Show |
3 | a0001c0001t0008g0266a0001c0001t0008g0294a0001c0001t0076g0293 | 3 | HG01168.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.395-793_395-792ins others(2910): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448673 | |||||
chr1:24448673
|
C | CAAGAATG others(2904): Show |
3 | a0001c0001t0008g0292a0001c0001t0008g0302a0001c0001t0075g0291 | 3 | HG01255.hp1 HG01496.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.395-793_395-792ins others(2911): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448673 | |||||
chr1:24448673
|
C | CAAGAATG others(2904): Show |
2 | a0001c0001t0008g0023a0001c0001t0008g0295 | 3 | HG01070.hp1 HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.395-793_395-792ins others(2911): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 24448673 | |||||
chr1:24449002
|
C | T | 1 | a0001c0001t0049g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395-479C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449002 | ||||||
chr1:24449081
|
A | G | 2 | a0001c0001t0008g0292a0001c0001t0008g0294 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.395-400A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449081 | ||||||
chr1:24449232
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0012g0323 | 2 | HG00673.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.395-249A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449232 | ||||||
chr1:24449392
|
G | A | 5 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-89G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449392 | ||||||
chr1:24449457
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0034g0328 | 3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.395-24C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449457 | ||||||
chr1:24449477
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(61): Show | 75 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
splice_region_variant&intron_variant | LOW | c.395-4G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 5/11 | chr1 | 24449477 | ||||||
chr1:24449695
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.540+69G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24449695 | ||||||
chr1:24449755
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.540+129C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24449755 | ||||||
chr1:24450087
|
A | G | 2 | a0001c0001t0008g0023a0001c0001t0008g0295 | 3 | HG01070.hp1 HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.540+461A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450087 | ||||||
chr1:24450095
|
G | A | 12 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0016g0167others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.540+469G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450095 | ||||||
chr1:24450108
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.540+482C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450108 | ||||||
chr1:24450114
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0034g0328 | 3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.540+488C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450114 | ||||||
chr1:24450237
|
G | A | 10 | a0001c0001t0006g0146a0001c0001t0011g0147a0001c0001t0016g0167others(7): Show | 10 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+611G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450237 | ||||||
chr1:24450307
|
C | T | 27 | a0001c0001t0006g0146a0001c0001t0007g0018a0001c0001t0007g0019others(24): Show | 28 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.540+681C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450307 | ||||||
chr1:24450452
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.540+826C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450452 | ||||||
chr1:24450481
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(61): Show | 75 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.540+855T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450481 | ||||||
chr1:24450609
|
C | T | 12 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(9): Show | 13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+983C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450609 | ||||||
chr1:24450677
|
G | C | 1 | a0001c0001t0004g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540+1051G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450677 | ||||||
chr1:24450723
|
G | A | 1 | a0001c0001t0032g0159 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.540+1097G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24450723 | ||||||
chr1:24451026
|
A | T | 1 | a0001c0002t0001g0058 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.540+1400A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451026 | ||||||
chr1:24451083
|
G | A | 15 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0004g0003others(12): Show | 21 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.540+1457G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451083 | ||||||
chr1:24451155
|
T | C | 39 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(36): Show | 46 | HG00733.hp1 HG01106.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.540+1529T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451155 | ||||||
chr1:24451351
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.540+1725C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451351 | ||||||
chr1:24451356
|
A | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.540+1730A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451356 | ||||||
chr1:24451525
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.541-1883G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451525 | ||||||
chr1:24451799
|
A | G | 344 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(341): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.541-1609A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451799 | ||||||
chr1:24451917
|
A | G | 1 | a0001c0002t0003g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.541-1491A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451917 | ||||||
chr1:24451970
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.541-1438C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24451970 | ||||||
chr1:24452145
|
T | C | 1 | a0001c0001t0017g0026 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.541-1263T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452145 | ||||||
chr1:24452321
|
A | G | 128 | a0001c0001t0012g0041a0001c0001t0017g0026a0001c0002t0001g0009others(125): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.541-1087A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452321 | ||||||
chr1:24452335
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(63): Show | 77 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-1073G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452335 | ||||||
chr1:24452369
|
C | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.541-1039C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452369 | ||||||
chr1:24452372
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.541-1036C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452372 | ||||||
chr1:24452458
|
C | T | 23 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(20): Show | 25 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.541-950C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452458 | ||||||
chr1:24452675
|
T | A | 3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.541-733T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452675 | ||||||
chr1:24452748
|
C | T | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.541-660C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452748 | ||||||
chr1:24452778
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.541-630C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452778 | ||||||
chr1:24452843
|
C | T | 8 | a0001c0002t0001g0013a0001c0002t0001g0078a0001c0002t0002g0013others(5): Show | 8 | NA18942.hp2 NA18963.hp2 NA19005.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-565C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452843 | ||||||
chr1:24452853
|
A | AT | 200 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(197): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.541-535dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 24452853 | |||||
chr1:24452853
|
A | ATT | 32 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0299others(29): Show | 33 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.541-536_541-535dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 24452853 | |||||
chr1:24452853
|
A | ATTT | 28 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(25): Show | 30 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.541-537_541-535dup others(3): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 24452853 | |||||
chr1:24452892
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(95): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.541-516G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452892 | ||||||
chr1:24452894
|
G | A | 160 | a0001c0001t0006g0146a0001c0001t0007g0018a0001c0001t0007g0019others(157): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.541-514G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452894 | ||||||
chr1:24452969
|
T | G | 8 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0160others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-439T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452969 | ||||||
chr1:24452992
|
G | A | 1 | a0001c0001t0023g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.541-416G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24452992 | ||||||
chr1:24453189
|
C | G | 128 | a0001c0001t0012g0041a0001c0001t0066g0135a0001c0002t0001g0009others(125): Show | 132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.541-219C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453189 | ||||||
chr1:24453359
|
G | A | 1 | a0001c0001t0038g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.541-49G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453359 | ||||||
chr1:24453365
|
T | C | 129 | a0001c0001t0001g0164a0001c0001t0012g0041a0001c0001t0017g0026others(126): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.541-43T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453365 | ||||||
chr1:24453383
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(97): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.541-25C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453383 | ||||||
chr1:24453397
|
G | T | 1 | a0003c0009t0012g0094 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.541-11G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453397 | ||||||
chr1:24453404
|
A | C | 1 | a0003c0009t0012g0094 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.541-4A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 6/11 | chr1 | 24453404 | ||||||
chr1:24453508
|
A | C | 1 | a0003c0009t0012g0094 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.637+4A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453508 | ||||||
chr1:24453586
|
A | G | 1 | a0001c0001t0008g0241 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637+82A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453586 | ||||||
chr1:24453710
|
A | C | 1 | a0003c0009t0012g0094 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.637+206A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453710 | ||||||
chr1:24453746
|
T | C | 2 | a0001c0002t0003g0128a0001c0002t0003g0129 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.637+242T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453746 | ||||||
chr1:24453856
|
C | T | 1 | a0001c0002t0027g0065 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.637+352C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453856 | ||||||
chr1:24453866
|
C | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(59): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.637+362C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24453866 | ||||||
chr1:24454031
|
C | CT | 129 | a0001c0001t0002g0205a0001c0001t0012g0041a0001c0001t0017g0026others(126): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.637+542dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 24454031 | |||||
chr1:24454031
|
C | CTT | 7 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(4): Show | 7 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.637+541_637+542dup others(2): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 24454031 | |||||
chr1:24454031
|
CT | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(133): Show | 157 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.637+542delT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 24454031 | |||||
chr1:24454253
|
A | G | 6 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(3): Show | 6 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+749A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454253 | ||||||
chr1:24454260
|
A | C | 1 | a0003c0009t0012g0094 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.637+756A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454260 | ||||||
chr1:24454380
|
G | C | 12 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(9): Show | 13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.637+876G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454380 | ||||||
chr1:24454437
|
G | A | 13 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(10): Show | 14 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+933G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454437 | ||||||
chr1:24454674
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(88): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.637+1170T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454674 | ||||||
chr1:24454757
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(225): Show | 245 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.637+1253T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454757 | ||||||
chr1:24454903
|
G | A | 1 | a0001c0001t0051g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.638-1235G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454903 | ||||||
chr1:24454933
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0034g0328 | 3 | HG02109.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638-1205G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454933 | ||||||
chr1:24454992
|
A | G | 1 | a0001c0001t0016g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.638-1146A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24454992 | ||||||
chr1:24455163
|
G | A | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.638-975G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455163 | ||||||
chr1:24455319
|
G | A | 3 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0055g0030 | 3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.638-819G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455319 | ||||||
chr1:24455364
|
T | C | 37 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(34): Show | 40 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.638-774T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455364 | ||||||
chr1:24455607
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0006g0146others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-531C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455607 | ||||||
chr1:24455668
|
A | G | 4 | a0001c0002t0001g0084a0001c0002t0001g0089a0001c0002t0001g0101others(1): Show | 4 | HG03490.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-470A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455668 | ||||||
chr1:24455722
|
C | A | 2 | a0001c0001t0006g0146a0001c0001t0035g0145 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.638-416C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455722 | ||||||
chr1:24455796
|
C | T | 4 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-342C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455796 | ||||||
chr1:24455800
|
T | C | 1 | a0001c0001t0038g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.638-338T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455800 | ||||||
chr1:24455850
|
C | A | 2 | a0001c0002t0001g0055a0001c0002t0001g0127 | 2 | HG01993.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.638-288C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455850 | ||||||
chr1:24455998
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.638-140G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24455998 | ||||||
chr1:24456036
|
C | T | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.638-102C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456036 | ||||||
chr1:24456078
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.638-60C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456078 | ||||||
chr1:24456079
|
G | A | 1 | a0001c0002t0003g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.638-59G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456079 | ||||||
chr1:24456133
|
T | C | 2 | a0001c0001t0064g0140a0001c0001t0065g0141 | 2 | HG00639.hp2 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.638-5T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 7/11 | chr1 | 24456133 | ||||||
chr1:24456278
|
G | A | 1 | a0001c0001t0008g0295 | 1 | HG01361.hp2 | splice_region_variant&intron_variant | LOW | c.773+5G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456278 | ||||||
chr1:24456440
|
G | A | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+167G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456440 | ||||||
chr1:24456493
|
G | C | 2 | a0001c0001t0030g0139a0001c0001t0030g0142 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.773+220G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456493 | ||||||
chr1:24456532
|
C | T | 1 | a0001c0001t0005g0274 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.773+259C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456532 | ||||||
chr1:24456656
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.773+383A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456656 | ||||||
chr1:24456701
|
G | A | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+428G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456701 | ||||||
chr1:24456821
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(260): Show | 283 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.773+548A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456821 | ||||||
chr1:24456902
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(68): Show | 82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.773+629A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456902 | ||||||
chr1:24456910
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(223): Show | 243 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.773+637A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24456910 | ||||||
chr1:24457195
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.773+922T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457195 | ||||||
chr1:24457379
|
T | G | 1 | a0001c0001t0001g0300 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.773+1106T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457379 | ||||||
chr1:24457428
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02027.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.773+1155G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457428 | ||||||
chr1:24457501
|
C | T | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.773+1228C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457501 | ||||||
chr1:24457545
|
T | C | 12 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(9): Show | 18 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.773+1272T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457545 | ||||||
chr1:24457616
|
C | T | 1 | a0001c0002t0061g0108 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.774-1272C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457616 | ||||||
chr1:24457649
|
A | G | 149 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0002g0035others(146): Show | 154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.774-1239A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457649 | ||||||
chr1:24457707
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(223): Show | 243 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.774-1181T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457707 | ||||||
chr1:24457724
|
G | A | 15 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(12): Show | 17 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.774-1164G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457724 | ||||||
chr1:24457785
|
A | C | 1 | a0001c0001t0010g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.774-1103A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457785 | ||||||
chr1:24457796
|
A | G | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-1092A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457796 | ||||||
chr1:24457831
|
C | T | 1 | a0001c0002t0067g0224 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.774-1057C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24457831 | ||||||
chr1:24458276
|
G | A | 2 | a0001c0001t0064g0140a0001c0001t0065g0141 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.774-612G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458276 | ||||||
chr1:24458368
|
G | T | 1 | a0001c0001t0001g0270 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.774-520G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458368 | ||||||
chr1:24458447
|
C | T | 126 | a0001c0002t0001g0009a0001c0002t0001g0012a0001c0002t0001g0013others(123): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.774-441C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458447 | ||||||
chr1:24458572
|
G | A | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-316G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458572 | ||||||
chr1:24458577
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(74): Show | 89 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.774-311C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458577 | ||||||
chr1:24458579
|
G | A | 72 | a0001c0002t0001g0013a0001c0002t0001g0040a0001c0002t0001g0054others(69): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.774-309G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458579 | ||||||
chr1:24458616
|
G | A | 1 | a0001c0001t0008g0241 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.774-272G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458616 | ||||||
chr1:24458690
|
G | T | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-198G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 8/11 | chr1 | 24458690 | ||||||
chr1:24459130
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.862+154G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459130 | ||||||
chr1:24459336
|
G | A | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.862+360G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459336 | ||||||
chr1:24459414
|
A | T | 1 | a0001c0001t0020g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.862+438A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459414 | ||||||
chr1:24459456
|
A | AT | 7 | a0001c0002t0003g0109a0001c0002t0003g0128a0001c0002t0003g0129others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+489dupT | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 24459456 | |||||
chr1:24459868
|
G | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0206others(10): Show | 20 | HG02056.hp1 NA18942.hp1 NA18947.hp1 others(17): Show |
intron_variant | MODIFIER | c.863-613G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459868 | ||||||
chr1:24459944
|
C | G | 37 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0170others(34): Show | 41 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.863-537C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459944 | ||||||
chr1:24459973
|
C | T | 13 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0182others(10): Show | 14 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.863-508C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24459973 | ||||||
chr1:24460108
|
G | C | 1 | a0001c0003t0003g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863-373G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24460108 | ||||||
chr1:24460273
|
A | G | 10 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(7): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.863-208A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 9/11 | chr1 | 24460273 | ||||||
chr1:24460879
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.926+335C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24460879 | ||||||
chr1:24461088
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.926+544A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461088 | ||||||
chr1:24461283
|
T | C | 4 | a0001c0001t0021g0329a0001c0001t0021g0330a0001c0001t0021g0332others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+739T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461283 | ||||||
chr1:24461307
|
CGAGGCAG others(318): Show |
C | 5 | a0001c0001t0004g0005a0001c0001t0004g0150a0001c0001t0004g0151others(2): Show | 7 | HG01884.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+777_926+1101de others(1): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461307 | |||||
chr1:24461389
|
A | G | 5 | a0001c0001t0007g0019a0001c0001t0007g0182a0001c0001t0007g0188others(2): Show | 6 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.926+845A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461389 | ||||||
chr1:24461457
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(244): Show | 267 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.926+913A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461457 | ||||||
chr1:24461489
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(102): Show | 120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.926+945C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461489 | ||||||
chr1:24461542
|
C | CA | 9 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0008g0302others(6): Show | 9 | HG00639.hp1 HG01069.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.926+1014dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461542 | |||||
chr1:24461542
|
CA | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0008g0292others(8): Show | 11 | HG00639.hp2 HG01517.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.926+1014delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461542 | |||||
chr1:24461638
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(190): Show | 211 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.926+1094A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461638 | ||||||
chr1:24461701
|
T | A | 1 | a0001c0001t0022g0264 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.926+1157T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24461701 | ||||||
chr1:24461865
|
C | CA | 6 | a0001c0001t0004g0027a0001c0001t0064g0140a0001c0001t0065g0141others(3): Show | 6 | HG00639.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.926+1335dupA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24461865 | |||||
chr1:24462065
|
G | A | 7 | a0001c0002t0003g0109a0001c0002t0003g0128a0001c0002t0003g0129others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+1521G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462065 | ||||||
chr1:24462344
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0326 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.927-1682G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462344 | ||||||
chr1:24462374
|
C | T | 1 | a0001c0002t0001g0275 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927-1652C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462374 | ||||||
chr1:24462460
|
G | A | 22 | a0001c0001t0006g0146a0001c0002t0003g0014a0001c0002t0003g0050others(19): Show | 23 | HG00099.hp2 HG01123.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.927-1566G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462460 | ||||||
chr1:24462558
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.927-1468G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462558 | ||||||
chr1:24462565
|
G | A | 4 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0073g0036others(1): Show | 4 | HG02145.hp1 HG03486.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-1461G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462565 | ||||||
chr1:24462692
|
G | T | 5 | a0001c0001t0002g0256a0001c0001t0004g0006a0001c0001t0004g0257others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.927-1334G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462692 | ||||||
chr1:24462700
|
G | C | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.927-1326G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462700 | ||||||
chr1:24462869
|
G | A | 7 | a0001c0001t0017g0155a0001c0001t0022g0031a0001c0001t0022g0032others(4): Show | 7 | HG00639.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.927-1157G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462869 | ||||||
chr1:24462895
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(97): Show | 114 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.927-1131C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24462895 | ||||||
chr1:24462983
|
TAAAATAC others(9): Show |
T | 4 | a0001c0001t0021g0329a0001c0001t0021g0330a0001c0001t0021g0332others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-1028_927-1013d others(18): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 24462983 | |||||
chr1:24463124
|
G | C | 8 | a0001c0001t0016g0016a0001c0001t0016g0167a0001c0001t0016g0168others(5): Show | 10 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.927-902G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463124 | ||||||
chr1:24463154
|
C | A | 1 | a0001c0001t0050g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927-872C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463154 | ||||||
chr1:24463264
|
G | C | 1 | a0001c0001t0005g0274 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.927-762G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463264 | ||||||
chr1:24463299
|
G | T | 1 | a0001c0001t0002g0304 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.927-727G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463299 | ||||||
chr1:24463363
|
G | A | 2 | a0001c0001t0016g0167a0001c0001t0051g0166 | 2 | HG01255.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.927-663G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463363 | ||||||
chr1:24463472
|
G | A | 14 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(11): Show | 14 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.927-554G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463472 | ||||||
chr1:24463519
|
A | G | 14 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(11): Show | 14 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.927-507A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463519 | ||||||
chr1:24463576
|
C | G | 1 | a0001c0001t0004g0005 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.927-450C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463576 | ||||||
chr1:24463583
|
G | C | 1 | a0001c0002t0002g0060 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.927-443G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463583 | ||||||
chr1:24463651
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.927-375A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463651 | ||||||
chr1:24463681
|
G | A | 4 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-345G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463681 | ||||||
chr1:24463854
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0326 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.927-172C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463854 | ||||||
chr1:24463946
|
C | T | 4 | a0001c0001t0021g0329a0001c0001t0021g0330a0001c0001t0021g0332others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-80C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463946 | ||||||
chr1:24463974
|
C | T | 4 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0022g0264others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-52C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24463974 | ||||||
chr1:24464021
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG01515.hp1 | splice_region_variant&intron_variant | LOW | c.927-5C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 10/11 | chr1 | 24464021 | ||||||
chr1:24464167
|
A | C | 1 | a0001c0002t0006g0079 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1021+47A>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464167 | ||||||
chr1:24464208
|
C | T | 1 | a0001c0001t0054g0331 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1021+88C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464208 | ||||||
chr1:24464221
|
G | T | 1 | a0001c0001t0076g0293 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1021+101G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464221 | ||||||
chr1:24464299
|
G | A | 1 | a0001c0001t0021g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1021+179G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464299 | ||||||
chr1:24464460
|
G | T | 4 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0022g0264others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+340G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464460 | ||||||
chr1:24464550
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1021+430C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464550 | ||||||
chr1:24464934
|
T | A | 1 | a0001c0001t0024g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1021+814T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464934 | ||||||
chr1:24464976
|
C | T | 1 | a0001c0002t0003g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1021+856C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24464976 | ||||||
chr1:24465196
|
A | AGTGCATG others(7): Show |
106 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(103): Show | 121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1021+1085_1021+109 others(18): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465196 | |||||
chr1:24465342
|
C | G | 2 | a0001c0001t0011g0147a0001c0001t0011g0176 | 2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1021+1222C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465342 | ||||||
chr1:24465417
|
T | TTG | 4 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0004g0027others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1305_1021+130 others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465417 | |||||
chr1:24465425
|
G | GTA | 24 | a0001c0001t0002g0035a0001c0001t0002g0057a0001c0001t0004g0003others(21): Show | 30 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1021+1322_1021+132 others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465425 | |||||
chr1:24465425
|
G | GTATATA | 4 | a0001c0001t0021g0329a0001c0001t0021g0330a0001c0001t0021g0332others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1318_1021+132 others(10): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465425 | |||||
chr1:24465425
|
GTA | G | 8 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(5): Show | 8 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+1322_1021+132 others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24465425 | |||||
chr1:24465427
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(113): Show | 131 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1021+1307A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465427 | ||||||
chr1:24465441
|
A | G | 2 | a0001c0001t0017g0155a0001c0001t0017g0263 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1021+1321A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465441 | ||||||
chr1:24465617
|
C | T | 3 | a0001c0001t0001g0267a0001c0001t0017g0155a0001c0001t0017g0263 | 3 | HG01123.hp1 HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1021+1497C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465617 | ||||||
chr1:24465775
|
T | A | 4 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0022g0264others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+1655T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465775 | ||||||
chr1:24465834
|
A | T | 11 | a0001c0001t0004g0003a0001c0001t0004g0005a0001c0001t0004g0017others(8): Show | 17 | HG01884.hp2 HG01891.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1021+1714A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465834 | ||||||
chr1:24465927
|
T | C | 2 | a0001c0001t0017g0155a0001c0001t0017g0263 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1021+1807T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24465927 | ||||||
chr1:24466127
|
T | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(238): Show | 261 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1021+2007T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466127 | ||||||
chr1:24466164
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1021+2044C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466164 | ||||||
chr1:24466241
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1021+2121C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466241 | ||||||
chr1:24466285
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1021+2165A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466285 | ||||||
chr1:24466438
|
G | T | 10 | a0001c0001t0016g0016a0001c0001t0016g0167a0001c0001t0016g0168others(7): Show | 12 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+2318G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466438 | ||||||
chr1:24466473
|
C | T | 1 | a0001c0002t0001g0278 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1021+2353C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466473 | ||||||
chr1:24466629
|
C | A | 4 | a0001c0001t0013g0192a0001c0001t0013g0193a0001c0001t0013g0196others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-2357C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466629 | ||||||
chr1:24466666
|
C | T | 1 | a0001c0001t0068g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1022-2320C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466666 | ||||||
chr1:24466764
|
A | G | 1 | a0001c0001t0002g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1022-2222A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466764 | ||||||
chr1:24466795
|
T | A | 1 | a0001c0001t0009g0232 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1022-2191T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466795 | ||||||
chr1:24466803
|
G | A | 1 | a0001c0002t0003g0125 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1022-2183G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466803 | ||||||
chr1:24466807
|
C | A | 2 | a0001c0001t0017g0155a0001c0001t0017g0263 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1022-2179C>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466807 | ||||||
chr1:24466838
|
C | T | 14 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(11): Show | 14 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1022-2148C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466838 | ||||||
chr1:24466841
|
C | G | 1 | a0001c0001t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1022-2145C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466841 | ||||||
chr1:24466856
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(248): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1022-2130G>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466856 | ||||||
chr1:24466933
|
A | G | 15 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(12): Show | 15 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1022-2053A>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466933 | ||||||
chr1:24466949
|
G | A | 1 | a0001c0001t0009g0232 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1022-2037G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466949 | ||||||
chr1:24466978
|
C | T | 15 | a0001c0001t0002g0035a0001c0001t0020g0034a0001c0001t0020g0157others(12): Show | 15 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1022-2008C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466978 | ||||||
chr1:24466990
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(243): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1022-1996T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24466990 | ||||||
chr1:24467202
|
G | A | 1 | a0001c0002t0001g0105 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1022-1784G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467202 | ||||||
chr1:24467234
|
C | T | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1022-1752C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467234 | ||||||
chr1:24467307
|
CA | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0024others(221): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1022-1666delA | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24467307 | |||||
chr1:24467347
|
G | A | 10 | a0001c0002t0001g0013a0001c0002t0001g0078a0001c0002t0002g0013others(7): Show | 10 | HG02132.hp1 HG02135.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1022-1639G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467347 | ||||||
chr1:24467441
|
G | T | 2 | a0001c0001t0030g0139a0001c0001t0030g0142 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1022-1545G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467441 | ||||||
chr1:24467481
|
A | T | 74 | a0001c0001t0001g0029a0001c0001t0001g0326a0001c0001t0002g0215others(71): Show | 77 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1022-1505A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467481 | ||||||
chr1:24467520
|
C | G | 4 | a0001c0001t0024g0194a0001c0001t0024g0195a0001c0001t0034g0328others(1): Show | 4 | HG01106.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-1466C>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467520 | ||||||
chr1:24467529
|
T | C | 1 | a0001c0001t0002g0304 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1022-1457T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467529 | ||||||
chr1:24467638
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1022-1348G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467638 | ||||||
chr1:24467912
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1022-1074T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467912 | ||||||
chr1:24467943
|
A | T | 1 | a0001c0002t0001g0279 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1022-1043A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24467943 | ||||||
chr1:24468009
|
G | A | 1 | a0001c0001t0034g0328 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1022-977G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468009 | ||||||
chr1:24468064
|
T | G | 1 | a0001c0002t0001g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1022-922T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468064 | ||||||
chr1:24468071
|
T | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1022-915T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468071 | ||||||
chr1:24468314
|
C | CAATA | 11 | a0001c0001t0002g0206a0001c0001t0004g0028a0001c0001t0016g0167others(8): Show | 11 | HG02257.hp2 HG02723.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1022-649_1022-646d others(6): Show |
NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 24468314 | |||||
chr1:24468352
|
C | T | 9 | a0001c0001t0001g0316a0001c0001t0002g0035a0001c0001t0020g0034others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-634C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468352 | ||||||
chr1:24468353
|
G | A | 4 | a0001c0001t0022g0031a0001c0001t0022g0032a0001c0001t0022g0264others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-633G>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468353 | ||||||
chr1:24468489
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1022-497T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468489 | ||||||
chr1:24468591
|
T | C | 1 | a0001c0001t0052g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1022-395T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468591 | ||||||
chr1:24468604
|
G | T | 13 | a0001c0001t0020g0034a0001c0001t0020g0157a0001c0001t0020g0158others(10): Show | 13 | HG01099.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1022-382G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468604 | ||||||
chr1:24468700
|
C | T | 1 | a0001c0001t0074g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1022-286C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468700 | ||||||
chr1:24468702
|
C | T | 1 | a0001c0002t0003g0073 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1022-284C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468702 | ||||||
chr1:24468855
|
A | T | 1 | a0001c0002t0003g0098 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1022-131A>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468855 | ||||||
chr1:24468873
|
G | T | 1 | a0001c0001t0002g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1022-113G>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468873 | ||||||
chr1:24468878
|
T | G | 1 | a0001c0001t0002g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1022-108T>G | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468878 | ||||||
chr1:24468882
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1022-104T>C | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468882 | ||||||
chr1:24468906
|
C | T | 1 | a0001c0001t0029g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1022-80C>T | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468906 | ||||||
chr1:24468982
|
T | A | 1 | a0001c0001t0052g0175 | 1 | HG02809.hp1 | splice_region_variant&intron_variant | LOW | c.1022-4T>A | NIPAL3 | ENSG00000001461.17 | transcript | ENST00000374399.9 | protein_coding | 11/11 | chr1 | 24468982 |