geneid | 126147 |
---|---|
ensemblid | ENSG00000142233.14 |
hgncid | 25208 |
symbol | NTN5 |
name | netrin 5 |
refseq_nuc | NM_145807.4 |
refseq_prot | NP_665806.1 |
ensembl_nuc | ENST00000270235.11 |
ensembl_prot | ENSP00000270235.4 |
mane_status | MANE Select |
chr | chr19 |
start | 48661407 |
end | 48673017 |
strand | - |
ver | v1.2 |
region | chr19:48661407-48673017 |
region5000 | chr19:48656407-48678017 |
regionname0 | NTN5_chr19_48661407_48673017 |
regionname5000 | NTN5_chr19_48656407_48678017 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 489 | 398 | 89 | 71 | 185 | 12 | 40 | 151 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0002 | 0/0 | 489 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0003 | 0/0 | 489 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0004 | 0/1 | 489 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0005 | 0/0 | 489 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0006 | 0/0 | 489 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0007 | 0/0 | 489 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0008 | 0/0 | 489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1470 | 209 | 37 | 32 | 105 | 6 | 29 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0002 | 1/0 | 1470 | 163 | 47 | 35 | 69 | 2 | 9 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0003 | 0/0 | 1470 | 11 | 2 | 3 | 0 | 4 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0004 | 0/0 | 1470 | 8 | 0 | 0 | 8 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0005 | 0/0 | 1470 | 4 | 3 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0006 | 0/0 | 1470 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0007 | 0/0 | 1470 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0008 | 0/0 | 1470 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0009 | 0/1 | 1470 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0010 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0011 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0012 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0013 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0014 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0015 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
c0016 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 377 | 245 | 49 | 38 | 116 | 10 | 31 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
t0002 | 1/0 | 377 | 166 | 44 | 36 | 74 | 2 | 9 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
t0003 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 30 | 6 | 11 | 0 | 2 | 11 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0002 | 0/0 | 22 | 2 | 0 | 17 | 0 | 3 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0003 | 0/0 | 21 | 1 | 2 | 18 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0004 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0005 | 0/0 | 18 | 0 | 0 | 17 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0006 | 0/0 | 18 | 0 | 6 | 8 | 0 | 4 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0007 | 0/0 | 11 | 9 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0008 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0009 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0010 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0011 | 0/0 | 10 | 0 | 1 | 8 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0014 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0017 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0021 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0022 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0023 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0025 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0039 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1470 | 209 | 37 | 32 | 105 | 6 | 29 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0002 | 1/0 | 1470 | 163 | 47 | 35 | 69 | 2 | 9 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0003 | 0/0 | 1470 | 11 | 2 | 3 | 0 | 4 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0004 | 0/0 | 1470 | 8 | 0 | 0 | 8 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0007 | 0/0 | 1470 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0010 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0011 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0012 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0015 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0002c0005 | 0/0 | 1470 | 4 | 3 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0003c0006 | 0/0 | 1470 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0004c0009 | 0/1 | 1470 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0005c0008 | 0/0 | 1470 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0006c0016 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0007c0014 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0008c0013 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1846 | 208 | 36 | 32 | 105 | 6 | 29 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0001t0002 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0002t0001 | 0/0 | 1846 | 8 | 7 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0002t0002 | 1/0 | 1846 | 154 | 39 | 35 | 68 | 2 | 9 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0002t0003 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0003t0001 | 0/0 | 1846 | 11 | 2 | 3 | 0 | 4 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0004t0001 | 0/0 | 1846 | 8 | 0 | 0 | 8 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0007t0001 | 0/0 | 1846 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0010t0002 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0011t0002 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0012t0001 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0001c0015t0001 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0002c0005t0002 | 0/0 | 1846 | 4 | 3 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0003c0006t0002 | 0/0 | 1846 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0004c0009t0001 | 0/1 | 1846 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0005c0008t0001 | 0/0 | 1846 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0006c0016t0002 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0007c0014t0001 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
a0008c0013t0002 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | copy fasta | chr19 | 48656407 | 48678017 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 30 | 6 | 11 | 0 | 2 | 11 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0002 | 0/0 | 22 | 2 | 0 | 17 | 0 | 3 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0004 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0005 | 0/0 | 18 | 0 | 0 | 17 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0007 | 0/0 | 11 | 9 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0008 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0025 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0003 | 0/0 | 21 | 1 | 2 | 18 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0006 | 0/0 | 18 | 0 | 6 | 8 | 0 | 4 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0009 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0010 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0011 | 0/0 | 10 | 0 | 1 | 8 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0014 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0021 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0003t0001g0022 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0003t0001g0023 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0003t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0004t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0004t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0007t0001g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0010t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0011t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0012t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0001c0015t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0002c0005t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0002c0005t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0002c0005t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0003c0006t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0003c0006t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0004c0009t0001g0039 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0005c0008t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0006c0016t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0007c0014t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
a0008c0013t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00597 | hp2 | a0003 | c0006 | t0002 | g0123 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00621 | hp1 | a0006 | c0016 | t0002 | g0139 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01106 | hp1 | a0005 | c0008 | t0001 | g0037 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0150 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01346 | hp2 | a0002 | c0005 | t0002 | g0137 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01358 | hp2 | a0005 | c0008 | t0001 | g0037 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01433 | hp2 | a0001 | c0007 | t0001 | g0027 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0022 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0023 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0021 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0023 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0022 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0048 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0151 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0134 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02145 | hp2 | a0001 | c0007 | t0001 | g0027 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0124 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02818 | hp2 | a0001 | c0007 | t0001 | g0027 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02886 | hp1 | a0002 | c0005 | t0002 | g0049 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02922 | hp2 | a0001 | c0012 | t0001 | g0107 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03139 | hp2 | a0008 | c0013 | t0002 | g0130 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0157 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03453 | hp2 | a0002 | c0005 | t0002 | g0142 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0022 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0117 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0116 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18612 | hp2 | a0001 | c0011 | t0002 | g0133 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18949 | hp1 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18950 | hp1 | a0003 | c0006 | t0002 | g0045 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18961 | hp2 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18971 | hp2 | a0001 | c0015 | t0001 | g0073 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18972 | hp1 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19007 | hp2 | a0003 | c0006 | t0002 | g0045 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19009 | hp1 | a0001 | c0010 | t0002 | g0132 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19011 | hp1 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19030 | hp1 | a0002 | c0005 | t0002 | g0049 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19060 | hp2 | a0001 | c0004 | t0001 | g0106 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19065 | hp2 | a0007 | c0014 | t0001 | g0092 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19074 | hp1 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19085 | hp1 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ASW | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0143 | EUR | TSI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | GIH | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | GIH | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0118 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0048 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG06807 | hp1 | a0004 | c0009 | t0001 | g0039 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
homoSapiens_chm13v2 | hp1 | a0004 | c0009 | t0001 | g0039 | REF | REF | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0112 | REF | REF | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48661687
|
G | A | 1 | a0002 | 4 | HG01346.hp2 HG02886.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1460C>T | p.Pro487Leu | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1566/1846 | 1460/1470 | 487/489 | chr19 | 48661687 | ||
chr19:48661696
|
C | T | 1 | a0007 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1451G>A | p.Ser484Asn | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1557/1846 | 1451/1470 | 484/489 | chr19 | 48661696 | ||
chr19:48661900
|
A | C | 1 | a0003 | 3 | HG00597.hp2 NA18950.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.1247T>G | p.Leu416Arg | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1353/1846 | 1247/1470 | 416/489 | chr19 | 48661900 | ||
chr19:48661960
|
T | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1187A>G | p.Lys396Arg | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1293/1846 | 1187/1470 | 396/489 | chr19 | 48661960 | ||
chr19:48661961
|
T | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1186A>G | p.Lys396Glu | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1292/1846 | 1186/1470 | 396/489 | chr19 | 48661961 | ||
chr19:48661962
|
G | C | 1 | a0006 | 1 | HG00621.hp1 | stop_gained | HIGH | c.1185C>G | p.Tyr395* | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1291/1846 | 1185/1470 | 395/489 | chr19 | 48661962 | ||
chr19:48661963
|
T | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1184A>G | p.Tyr395Cys | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1290/1846 | 1184/1470 | 395/489 | chr19 | 48661963 | ||
chr19:48661964
|
A | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1183T>G | p.Tyr395Asp | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1289/1846 | 1183/1470 | 395/489 | chr19 | 48661964 | ||
chr19:48661966
|
A | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1181T>G | p.Val394Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1287/1846 | 1181/1470 | 394/489 | chr19 | 48661966 | ||
chr19:48661969
|
G | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1178C>G | p.Ala393Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1284/1846 | 1178/1470 | 393/489 | chr19 | 48661969 | ||
chr19:48661972
|
A | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1175T>G | p.Leu392Arg | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1281/1846 | 1175/1470 | 392/489 | chr19 | 48661972 | ||
chr19:48661973
|
G | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1174C>G | p.Leu392Val | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1280/1846 | 1174/1470 | 392/489 | chr19 | 48661973 | ||
chr19:48662015
|
C | T | 1 | a0008 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1132G>A | p.Glu378Lys | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1238/1846 | 1132/1470 | 378/489 | chr19 | 48662015 | ||
chr19:48663484
|
T | C | 1 | a0004 | 2 | HG06807.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.1084A>G | p.Arg362Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/7 | 1190/1846 | 1084/1470 | 362/489 | chr19 | 48663484 | ||
chr19:48664274
|
A | G | 1 | a0005 | 2 | HG01106.hp1 HG01358.hp2 |
missense_variant | MODERATE | c.839T>C | p.Ile280Thr | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/7 | 945/1846 | 839/1470 | 280/489 | chr19 | 48664274 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48661695
|
A | G | 6 | a0001c0001a0001c0007a0001c0015others(3): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
synonymous_variant | LOW | c.1452T>C | p.Ser484Ser | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1558/1846 | 1452/1470 | 484/489 | chr19 | 48661695 | ||
chr19:48661698
|
G | T | 1 | a0001c0007 | 3 | HG01433.hp2 HG02145.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1449C>A | p.Pro483Pro | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1555/1846 | 1449/1470 | 483/489 | chr19 | 48661698 | ||
chr19:48661890
|
G | C | 1 | a0001c0015 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1257C>G | p.Gly419Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1363/1846 | 1257/1470 | 419/489 | chr19 | 48661890 | ||
chr19:48661965
|
A | C | 1 | a0006c0016 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.1182T>G | p.Val394Val | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1288/1846 | 1182/1470 | 394/489 | chr19 | 48661965 | ||
chr19:48661968
|
G | C | 1 | a0006c0016 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.1179C>G | p.Ala393Ala | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1285/1846 | 1179/1470 | 393/489 | chr19 | 48661968 | ||
chr19:48662001
|
C | G | 1 | a0001c0012 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1146G>C | p.Pro382Pro | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1252/1846 | 1146/1470 | 382/489 | chr19 | 48662001 | ||
chr19:48664748
|
G | A | 1 | a0001c0003 | 11 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
synonymous_variant | LOW | c.651C>T | p.His217His | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/7 | 757/1846 | 651/1470 | 217/489 | chr19 | 48664748 | ||
chr19:48670414
|
C | T | 2 | a0001c0004a0001c0012 | 9 | HG02922.hp2 NA18949.hp1 NA18952.hp2 others(6): Show |
synonymous_variant | LOW | c.573G>A | p.Pro191Pro | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/7 | 679/1846 | 573/1470 | 191/489 | chr19 | 48670414 | ||
chr19:48670540
|
C | T | 1 | a0001c0011 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.447G>A | p.Ala149Ala | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/7 | 553/1846 | 447/1470 | 149/489 | chr19 | 48670540 | ||
chr19:48670585
|
C | T | 1 | a0001c0010 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.402G>A | p.Ala134Ala | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/7 | 508/1846 | 402/1470 | 134/489 | chr19 | 48670585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48661483
|
T | C | 10 | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(7): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*194A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 194 | chr19 | 48661483 | |||||
chr19:48673003
|
C | A | 1 | a0001c0002t0003 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/7 | 2017 | chr19 | 48673003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48662066
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1106-25G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662066 | ||||||
chr19:48662307
|
T | TGCA | 3 | a0001c0002t0002g0010a0001c0002t0002g0046a0001c0002t0003g0157 | 13 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1106-267_1106-266i others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662307 | ||||||
chr19:48662308
|
A | T | 3 | a0001c0002t0002g0010a0001c0002t0002g0046a0001c0002t0003g0157 | 13 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1106-267T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662308 | ||||||
chr19:48662356
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1106-315C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662356 | ||||||
chr19:48662510
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1106-469T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662510 | ||||||
chr19:48662819
|
G | GGAGATCC others(90): Show |
1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1105+547_1105+643d others(99): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662819 | ||||||
chr19:48663019
|
T | C | 1 | a0001c0002t0002g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1105+444A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663019 | ||||||
chr19:48663033
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0125 | 3 | HG01070.hp1 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1105+430A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663033 | ||||||
chr19:48663054
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1105+409C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663054 | ||||||
chr19:48663063
|
G | A | 1 | a0001c0002t0002g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1105+400C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663063 | ||||||
chr19:48663286
|
C | T | 1 | a0001c0002t0002g0020 | 4 | HG02622.hp2 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+177G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663286 | ||||||
chr19:48663618
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1025-75C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 5/6 | chr19 | 48663618 | ||||||
chr19:48663840
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.971-26G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48663840 | ||||||
chr19:48663876
|
C | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0002g0010others(2): Show | 15 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-62G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48663876 | ||||||
chr19:48664006
|
G | A | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.970+137C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48664006 | ||||||
chr19:48664085
|
C | G | 1 | a0001c0002t0002g0030 | 3 | NA18960.hp1 NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.970+58G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48664085 | ||||||
chr19:48664104
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0076others(8): Show | 23 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.970+39C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48664104 | ||||||
chr19:48664416
|
GGAGTCCA others(29): Show |
G | 3 | a0001c0001t0001g0091a0001c0002t0002g0119a0001c0002t0002g0121 | 3 | NA18747.hp1 NA18954.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.820+127_821-125del others(36): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664416 | ||||||
chr19:48664426
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.821-134G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664426 | ||||||
chr19:48664521
|
C | A | 1 | a0001c0003t0001g0053 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.820+58G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664521 | ||||||
chr19:48664522
|
C | T | 1 | a0001c0003t0001g0053 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.820+57G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664522 | ||||||
chr19:48664529
|
G | A | 1 | a0001c0003t0001g0053 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.820+50C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664529 | ||||||
chr19:48664851
|
C | T | 1 | a0001c0004t0001g0029 | 3 | NA18961.hp2 NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.632-84G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664851 | ||||||
chr19:48664925
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.632-158A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664925 | ||||||
chr19:48664936
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0087a0001c0001t0001g0099others(1): Show | 6 | HG01074.hp2 HG02735.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.632-169C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664936 | ||||||
chr19:48664973
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.632-206G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664973 | ||||||
chr19:48665079
|
A | AT | 6 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0085others(3): Show | 8 | HG01934.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.632-313dupA | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665079 | ||||||
chr19:48665079
|
AT | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0097others(5): Show | 13 | HG02258.hp1 HG02615.hp1 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.632-313delA | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665079 | ||||||
chr19:48665135
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0094 | 11 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-368C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665135 | ||||||
chr19:48665139
|
G | T | 2 | a0001c0002t0002g0155a0001c0002t0002g0156 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.632-372C>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665139 | ||||||
chr19:48665171
|
C | T | 6 | a0001c0002t0002g0015a0001c0002t0002g0033a0001c0002t0002g0128others(3): Show | 12 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.632-404G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665171 | ||||||
chr19:48665202
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.632-435T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665202 | ||||||
chr19:48665300
|
A | G | 61 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0149others(58): Show | 146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.632-533T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665300 | ||||||
chr19:48665435
|
C | CA | 13 | a0001c0001t0001g0068a0001c0001t0001g0093a0001c0002t0002g0009others(10): Show | 25 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.632-669dupT | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665435 | ||||||
chr19:48665480
|
G | A | 61 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0149others(58): Show | 146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.632-713C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665480 | ||||||
chr19:48665540
|
TC | T | 3 | a0001c0002t0001g0054a0001c0002t0001g0153a0001c0002t0001g0154 | 4 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-774delG | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665540 | ||||||
chr19:48665543
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(151): Show | 408 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(405): Show |
intron_variant | MODIFIER | c.632-776T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665543 | ||||||
chr19:48665685
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.632-918C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665685 | ||||||
chr19:48665833
|
C | A | 2 | a0001c0002t0002g0020a0001c0002t0002g0050 | 6 | HG02486.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.632-1066G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665833 | ||||||
chr19:48665959
|
TG | T | 52 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0149others(49): Show | 128 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.632-1193delC | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665959 | ||||||
chr19:48666259
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.632-1492C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666259 | ||||||
chr19:48666455
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.632-1688C>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666455 | ||||||
chr19:48666677
|
CTT | C | 20 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0041others(17): Show | 30 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.632-1912_632-1911d others(4): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666677 | ||||||
chr19:48666677
|
CTTT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(101): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.632-1913_632-1911d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666677 | ||||||
chr19:48666677
|
CTTTT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0094a0001c0001t0001g0102others(5): Show | 15 | HG01106.hp2 HG01167.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.632-1914_632-1911d others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666677 | ||||||
chr19:48666807
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0057 | 3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.632-2040G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666807 | ||||||
chr19:48666811
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(48): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.632-2044C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666811 | ||||||
chr19:48666836
|
A | G | 1 | a0001c0002t0002g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.632-2069T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666836 | ||||||
chr19:48666874
|
G | A | 2 | a0001c0002t0001g0034a0001c0002t0001g0057 | 3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.632-2107C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666874 | ||||||
chr19:48666960
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.632-2193G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666960 | ||||||
chr19:48667056
|
C | G | 2 | a0001c0002t0001g0034a0001c0002t0001g0057 | 3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.632-2289G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667056 | ||||||
chr19:48667211
|
C | A | 34 | a0001c0001t0001g0149a0001c0001t0002g0145a0001c0002t0002g0003others(31): Show | 89 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.632-2444G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667211 | ||||||
chr19:48667236
|
AGAG | A | 5 | a0001c0002t0001g0109a0001c0004t0001g0019a0001c0004t0001g0029others(2): Show | 10 | HG02027.hp1 HG02922.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.632-2472_632-2470d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667236 | ||||||
chr19:48667306
|
C | T | 1 | a0001c0002t0002g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.632-2539G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667306 | ||||||
chr19:48667778
|
C | G | 8 | a0001c0001t0001g0055a0001c0002t0001g0054a0001c0002t0001g0153others(5): Show | 17 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+2578G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667778 | ||||||
chr19:48667938
|
G | A | 1 | a0001c0002t0002g0141 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.631+2418C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667938 | ||||||
chr19:48668049
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(7): Show | 46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.631+2307G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668049 | ||||||
chr19:48668122
|
G | T | 1 | a0001c0002t0002g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.631+2234C>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668122 | ||||||
chr19:48668336
|
T | C | 52 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0149others(49): Show | 128 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.631+2020A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668336 | ||||||
chr19:48668404
|
GC | G | 2 | a0001c0002t0002g0020a0001c0002t0002g0050 | 6 | HG02486.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1951delG | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668404 | ||||||
chr19:48668749
|
G | A | 2 | a0001c0002t0002g0155a0001c0002t0002g0156 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.631+1607C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668749 | ||||||
chr19:48668849
|
C | T | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1507G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668849 | ||||||
chr19:48668857
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.631+1499T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668857 | ||||||
chr19:48668899
|
C | G | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1457G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668899 | ||||||
chr19:48668909
|
G | A | 4 | a0001c0001t0001g0055a0001c0002t0001g0054a0001c0002t0001g0153others(1): Show | 6 | HG01070.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1447C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668909 | ||||||
chr19:48668921
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0057 | 3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1435G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668921 | ||||||
chr19:48668938
|
T | A | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1418A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668938 | ||||||
chr19:48668945
|
C | A | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1411G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668945 | ||||||
chr19:48668949
|
A | G | 2 | a0001c0002t0001g0034a0001c0002t0001g0057 | 3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1407T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668949 | ||||||
chr19:48668956
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1400A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668956 | ||||||
chr19:48668963
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1393A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668963 | ||||||
chr19:48668963
|
TATCACCA others(5): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.631+1381_631+1392d others(14): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668963 | ||||||
chr19:48668965
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1391A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668965 | ||||||
chr19:48668966
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1390G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668966 | ||||||
chr19:48668968
|
C | T | 2 | a0001c0001t0001g0058a0003c0006t0002g0123 | 2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1388G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668968 | ||||||
chr19:48668969
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1387G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668969 | ||||||
chr19:48668972
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1384G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668972 | ||||||
chr19:48668975
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1381G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668975 | ||||||
chr19:48668978
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1378G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668978 | ||||||
chr19:48668979
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1377T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668979 | ||||||
chr19:48668980
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1376G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668980 | ||||||
chr19:48668981
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1375G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668981 | ||||||
chr19:48668983
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1373G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668983 | ||||||
chr19:48668987
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1369G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668987 | ||||||
chr19:48668989
|
C | T | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1367G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668989 | ||||||
chr19:48668992
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1364A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668992 | ||||||
chr19:48669001
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1355A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669001 | ||||||
chr19:48669002
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1354G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669002 | ||||||
chr19:48669004
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1352G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669004 | ||||||
chr19:48669008
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1348A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669008 | ||||||
chr19:48669009
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1347T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669009 | ||||||
chr19:48669011
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1345G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669011 | ||||||
chr19:48669018
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1338T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669018 | ||||||
chr19:48669025
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1331G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669025 | ||||||
chr19:48669029
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1327A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669029 | ||||||
chr19:48669035
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1321A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669035 | ||||||
chr19:48669040
|
T | A | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1316A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669040 | ||||||
chr19:48669040
|
TCACCACC others(608): Show |
T | 3 | a0001c0002t0002g0015a0001c0002t0002g0128a0001c0002t0002g0129 | 7 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+701_631+1315de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669040 | ||||||
chr19:48669045
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1311T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669045 | ||||||
chr19:48669046
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1310G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669046 | ||||||
chr19:48669049
|
C | T | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1307G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669049 | ||||||
chr19:48669055
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1301G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669055 | ||||||
chr19:48669058
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1298A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669058 | ||||||
chr19:48669058
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1298A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669058 | ||||||
chr19:48669061
|
C | T | 2 | a0001c0002t0002g0131a0008c0013t0002g0130 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+1295G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669061 | ||||||
chr19:48669065
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1291G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669065 | ||||||
chr19:48669067
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1289G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669067 | ||||||
chr19:48669067
|
CCACCACT others(23): Show |
C | 1 | a0001c0002t0002g0122 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.631+1259_631+1288d others(32): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669067 | ||||||
chr19:48669070
|
C | T | 3 | a0001c0002t0002g0131a0003c0006t0002g0123a0008c0013t0002g0130 | 3 | HG00597.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+1286G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669070 | ||||||
chr19:48669073
|
CTATCACC others(274): Show |
C | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+1002_631+1282d others(2): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669073 | ||||||
chr19:48669074
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+1282A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669074 | ||||||
chr19:48669076
|
T | C | 2 | a0001c0002t0002g0131a0003c0006t0002g0123 | 2 | HG00597.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.631+1280A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669076 | ||||||
chr19:48669076
|
TCACCATC others(41): Show |
T | 1 | a0001c0002t0002g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.631+1232_631+1279d others(50): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669076 | ||||||
chr19:48669085
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1271A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669085 | ||||||
chr19:48669085
|
TCACCACC others(469): Show |
T | 1 | a0001c0002t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+795_631+1270de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669085 | ||||||
chr19:48669088
|
C | T | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1268G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669088 | ||||||
chr19:48669104
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1252A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669104 | ||||||
chr19:48669105
|
A | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1251T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669105 | ||||||
chr19:48669106
|
T | A | 2 | a0001c0001t0001g0058a0003c0006t0002g0123 | 2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1250A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669106 | ||||||
chr19:48669108
|
A | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1248T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669108 | ||||||
chr19:48669109
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1247G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669109 | ||||||
chr19:48669112
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1244A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669112 | ||||||
chr19:48669115
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1241A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669115 | ||||||
chr19:48669121
|
C | T | 2 | a0001c0001t0001g0058a0003c0006t0002g0123 | 2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1235G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669121 | ||||||
chr19:48669127
|
C | T | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1229G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669127 | ||||||
chr19:48669133
|
T | C | 2 | a0001c0001t0001g0058a0003c0006t0002g0123 | 2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1223A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669133 | ||||||
chr19:48669136
|
T | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1220A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669136 | ||||||
chr19:48669144
|
TCATCACC others(489): Show |
T | 1 | a0001c0004t0001g0106 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.631+716_631+1211de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669144 | ||||||
chr19:48669147
|
T | C | 2 | a0001c0001t0001g0058a0003c0006t0002g0123 | 2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1209A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669147 | ||||||
chr19:48669150
|
CCACCATC others(272): Show |
C | 1 | a0001c0001t0001g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.631+927_631+1205de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669150 | ||||||
chr19:48669152
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1204T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669152 | ||||||
chr19:48669153
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1203G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669153 | ||||||
chr19:48669153
|
CCATCACC others(269): Show |
C | 1 | a0001c0002t0002g0150 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.631+927_631+1202de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669153 | ||||||
chr19:48669156
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.631+1200A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669156 | ||||||
chr19:48669158
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1198T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669158 | ||||||
chr19:48669165
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1191G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669165 | ||||||
chr19:48669171
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1185A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669171 | ||||||
chr19:48669176
|
ACCATGAC others(54): Show |
A | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1119_631+1179d others(63): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669176 | ||||||
chr19:48669181
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1175C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669181 | ||||||
chr19:48669195
|
CCACCATC others(7): Show |
C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1147_631+1160d others(16): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669195 | ||||||
chr19:48669198
|
CCATCACC others(26): Show |
C | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(42): Show | 115 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.631+1125_631+1157d others(35): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669198 | ||||||
chr19:48669198
|
CCATCACC others(62): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631+1089_631+1157d others(71): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669198 | ||||||
chr19:48669201
|
T | TCAC | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(50): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.631+1152_631+1154d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669201 | ||||||
chr19:48669201
|
TCACCATC others(35): Show |
T | 4 | a0001c0001t0001g0055a0001c0002t0001g0054a0001c0002t0001g0153others(1): Show | 6 | HG01070.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1113_631+1154d others(44): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669201 | ||||||
chr19:48669201
|
TCACCATC others(122): Show |
T | 4 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(1): Show | 14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+1026_631+1154d others(2): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669201 | ||||||
chr19:48669204
|
C | CCACCATC others(347): Show |
1 | a0001c0001t0001g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631+1151_631+1152i others(356): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669204 | ||||||
chr19:48669207
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0024others(6): Show | 32 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.631+1149A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669207 | ||||||
chr19:48669210
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1146G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669210 | ||||||
chr19:48669213
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(51): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.631+1143G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669213 | ||||||
chr19:48669216
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0024others(6): Show | 32 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.631+1140G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669216 | ||||||
chr19:48669222
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1134G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669222 | ||||||
chr19:48669223
|
C | G | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1133G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669223 | ||||||
chr19:48669225
|
CGACCAT | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0066 | 4 | HG00438.hp2 HG02040.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+1125_631+1130d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669225 | ||||||
chr19:48669225
|
CGACCATC others(323): Show |
C | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(9): Show | 54 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+801_631+1130de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669225 | ||||||
chr19:48669226
|
G | C | 2 | a0001c0001t0001g0095a0001c0002t0001g0034 | 3 | HG01891.hp1 HG02080.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1130C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669226 | ||||||
chr19:48669231
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631+1125A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669231 | ||||||
chr19:48669234
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1122A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669234 | ||||||
chr19:48669240
|
C | CCACCACC others(41): Show |
2 | a0001c0001t0001g0017a0001c0002t0002g0052 | 6 | HG00280.hp1 HG01081.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1115_631+1116i others(50): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669240 | ||||||
chr19:48669240
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1116G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669240 | ||||||
chr19:48669243
|
C | CCACCACC others(32): Show |
1 | a0001c0002t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1112_631+1113i others(41): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | ||||||
chr19:48669243
|
C | CCACCATC others(50): Show |
1 | a0001c0002t0002g0141 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.631+1112_631+1113i others(59): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | ||||||
chr19:48669243
|
C | CCACCATC others(47): Show |
16 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0041others(13): Show | 60 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+1112_631+1113i others(56): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | ||||||
chr19:48669243
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(45): Show | 119 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.631+1113G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | ||||||
chr19:48669244
|
C | T | 1 | a0001c0002t0002g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.631+1112G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669244 | ||||||
chr19:48669246
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1110G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669246 | ||||||
chr19:48669246
|
CCATCACC others(71): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.631+1032_631+1109d others(80): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669246 | ||||||
chr19:48669248
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1108T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669248 | ||||||
chr19:48669249
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1107A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669249 | ||||||
chr19:48669249
|
T | C | 1 | a0001c0002t0002g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.631+1107A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669249 | ||||||
chr19:48669252
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1104G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669252 | ||||||
chr19:48669252
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1104G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669252 | ||||||
chr19:48669255
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1101G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669255 | ||||||
chr19:48669258
|
C | CCAT | 20 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(17): Show | 52 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(49): Show |
intron_variant | MODIFIER | c.631+1097_631+1098i others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | ||||||
chr19:48669258
|
C | CCATCACC others(23): Show |
1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.631+1097_631+1098i others(32): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | ||||||
chr19:48669258
|
C | CCATCACC others(250): Show |
1 | a0001c0001t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.631+1097_631+1098i others(259): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | ||||||
chr19:48669258
|
C | G | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1098G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | ||||||
chr19:48669258
|
CCACGACC others(2): Show |
C | 5 | a0001c0001t0001g0040a0001c0001t0001g0096a0001c0002t0002g0014others(2): Show | 12 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.631+1089_631+1097d others(11): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | ||||||
chr19:48669259
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1097G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669259 | ||||||
chr19:48669261
|
C | T | 3 | a0001c0001t0001g0075a0001c0002t0001g0034a0003c0006t0002g0123 | 4 | HG00597.hp2 HG00735.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+1095G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669261 | ||||||
chr19:48669262
|
G | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(26): Show | 62 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.631+1094C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669262 | ||||||
chr19:48669264
|
C | T | 1 | a0001c0002t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1092G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669264 | ||||||
chr19:48669267
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1089A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669267 | ||||||
chr19:48669267
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(42): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.631+1089A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669267 | ||||||
chr19:48669270
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(22): Show | 57 | HG00408.hp1 HG00544.hp1 HG01258.hp1 others(54): Show |
intron_variant | MODIFIER | c.631+1086A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669270 | ||||||
chr19:48669273
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(18): Show | 53 | HG00408.hp1 HG01258.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.631+1083G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669273 | ||||||
chr19:48669275
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1081T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669275 | ||||||
chr19:48669276
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0088 | 2 | HG00099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.631+1080G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669276 | ||||||
chr19:48669282
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+1074G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669282 | ||||||
chr19:48669285
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1071A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669285 | ||||||
chr19:48669285
|
T | C | 7 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0075others(4): Show | 8 | HG00544.hp1 HG00735.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+1071A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669285 | ||||||
chr19:48669285
|
TCACCACC others(104): Show |
T | 2 | a0001c0003t0001g0023a0001c0003t0001g0053 | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+960_631+1070de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669285 | ||||||
chr19:48669287
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1069T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669287 | ||||||
chr19:48669288
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(20): Show | 72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.631+1068G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669288 | ||||||
chr19:48669291
|
C | CCACCATC others(131): Show |
1 | a0001c0002t0002g0044 | 2 | HG03490.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.631+927_631+1064du others(139): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669291 | ||||||
chr19:48669294
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1062G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669294 | ||||||
chr19:48669294
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(18): Show | 54 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+1062G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669294 | ||||||
chr19:48669297
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(19): Show | 55 | HG00408.hp1 HG01258.hp1 HG01361.hp2 others(52): Show |
intron_variant | MODIFIER | c.631+1059A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669297 | ||||||
chr19:48669297
|
TCACCACC others(212): Show |
T | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.631+840_631+1058de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669297 | ||||||
chr19:48669303
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1053G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669303 | ||||||
chr19:48669303
|
CCACCACC others(2): Show |
C | 1 | a0001c0003t0001g0022 | 4 | HG01515.hp1 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1044_631+1052d others(11): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669303 | ||||||
chr19:48669304
|
C | G | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1052G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669304 | ||||||
chr19:48669306
|
C | CCATCAT | 19 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.631+1049_631+1050i others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669306 | ||||||
chr19:48669306
|
C | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0080a0001c0001t0001g0096others(3): Show | 12 | HG00544.hp1 HG01123.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.631+1050G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669306 | ||||||
chr19:48669307
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1049G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669307 | ||||||
chr19:48669308
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1048T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669308 | ||||||
chr19:48669309
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0065others(3): Show | 7 | HG00438.hp2 HG02040.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+1047G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669309 | ||||||
chr19:48669312
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(20): Show | 55 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.631+1044A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669312 | ||||||
chr19:48669312
|
TCACCAC | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0065others(1): Show | 5 | HG00438.hp2 HG02040.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1038_631+1043d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669312 | ||||||
chr19:48669315
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0002t0001g0034others(1): Show | 5 | HG00544.hp1 HG01261.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1041G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669315 | ||||||
chr19:48669318
|
C | T | 1 | a0001c0003t0001g0022 | 4 | HG01515.hp1 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1038G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669318 | ||||||
chr19:48669318
|
CCACCAT | C | 4 | a0001c0001t0001g0070a0001c0002t0002g0014a0001c0002t0002g0048others(1): Show | 10 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.631+1032_631+1037d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669318 | ||||||
chr19:48669319
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1037G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669319 | ||||||
chr19:48669320
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1036T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669320 | ||||||
chr19:48669324
|
T | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 65 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.631+1032A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | ||||||
chr19:48669324
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0081others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1032A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | ||||||
chr19:48669324
|
TCACCAC | T | 2 | a0001c0001t0001g0078a0001c0002t0001g0034 | 3 | HG01891.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1026_631+1031d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | ||||||
chr19:48669324
|
TCACCACC others(227): Show |
T | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0125others(2): Show | 5 | HG02148.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.631+798_631+1031de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | ||||||
chr19:48669327
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631+1029G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669327 | ||||||
chr19:48669327
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+1029G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669327 | ||||||
chr19:48669328
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1028G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669328 | ||||||
chr19:48669329
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1027T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669329 | ||||||
chr19:48669331
|
C | G | 3 | a0001c0002t0002g0014a0001c0002t0002g0048a0001c0002t0002g0135 | 9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+1025G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669331 | ||||||
chr19:48669333
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(43): Show | 119 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.631+1023G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669333 | ||||||
chr19:48669334
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1022G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669334 | ||||||
chr19:48669336
|
C | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0065others(1): Show | 5 | HG00438.hp2 HG02040.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1020G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | ||||||
chr19:48669336
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.631+1020G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | ||||||
chr19:48669336
|
CCAT | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(14): Show | 45 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.631+1017_631+1019d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | ||||||
chr19:48669336
|
CCATCACC others(224): Show |
C | 2 | a0001c0001t0001g0097a0002c0005t0002g0142 | 2 | HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.631+789_631+1019de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | ||||||
chr19:48669339
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 73 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.631+1017A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669339 | ||||||
chr19:48669342
|
C | CCAT | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0087 | 3 | HG02622.hp1 HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.631+1013_631+1014i others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669342 | ||||||
chr19:48669342
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(37): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.631+1014G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669342 | ||||||
chr19:48669342
|
CCACCACC others(227): Show |
C | 23 | a0001c0001t0001g0055a0001c0001t0002g0145a0001c0002t0001g0054others(20): Show | 68 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.631+780_631+1013de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669342 | ||||||
chr19:48669345
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(24): Show | 86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.631+1011G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669345 | ||||||
chr19:48669348
|
C | CCACGACC others(5): Show |
1 | a0001c0002t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1007_631+1008i others(14): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669348 | ||||||
chr19:48669348
|
C | CCATCACC others(295): Show |
1 | a0001c0001t0001g0012 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+1007_631+1008i others(304): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669348 | ||||||
chr19:48669348
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+1008G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669348 | ||||||
chr19:48669351
|
C | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(17): Show | 46 | HG00408.hp1 HG00735.hp1 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.631+1005G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669351 | ||||||
chr19:48669351
|
CCATCACC others(152): Show |
C | 1 | a0001c0003t0001g0022 | 4 | HG01515.hp1 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+846_631+1004de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669351 | ||||||
chr19:48669354
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 106 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.631+1002A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669354 | ||||||
chr19:48669355
|
C | G | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1001G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669355 | ||||||
chr19:48669357
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0065others(6): Show | 16 | HG00438.hp2 HG01123.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+999G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669357 | ||||||
chr19:48669358
|
C | G | 6 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(3): Show | 16 | HG01243.hp1 HG01884.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+998G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669358 | ||||||
chr19:48669360
|
C | CCATCACC others(107): Show |
1 | a0001c0002t0002g0146 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.631+995_631+996ins others(114): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669360 | ||||||
chr19:48669360
|
C | CCATCATC others(62): Show |
15 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(12): Show | 41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+995_631+996ins others(69): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669360 | ||||||
chr19:48669360
|
CCACCATC others(209): Show |
C | 1 | a0001c0001t0001g0036 | 2 | NA18966.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.631+780_631+995del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669360 | ||||||
chr19:48669363
|
C | T | 10 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 21 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.631+993G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669363 | ||||||
chr19:48669366
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+990A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669366 | ||||||
chr19:48669366
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.631+990A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669366 | ||||||
chr19:48669369
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+987G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669369 | ||||||
chr19:48669369
|
C | CCAT | 4 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00735.hp1 HG02293.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+986_631+987ins others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669369 | ||||||
chr19:48669369
|
C | T | 2 | a0001c0002t0002g0146a0001c0002t0002g0156 | 2 | HG01261.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.631+987G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669369 | ||||||
chr19:48669372
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(19): Show | 70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.631+984G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669372 | ||||||
chr19:48669373
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631+983G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669373 | ||||||
chr19:48669373
|
CACCACCA others(125): Show |
C | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+851_631+982del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669373 | ||||||
chr19:48669375
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(15): Show | 44 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.631+981G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669375 | ||||||
chr19:48669378
|
C | T | 4 | a0001c0001t0001g0065a0001c0002t0002g0014a0001c0002t0002g0048others(1): Show | 10 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.631+978G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669378 | ||||||
chr19:48669381
|
T | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00735.hp1 HG02293.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+975A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669381 | ||||||
chr19:48669381
|
T | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(14): Show | 43 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.631+975A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669381 | ||||||
chr19:48669381
|
TCACCACC others(14): Show |
T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+954_631+974del others(21): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669381 | ||||||
chr19:48669384
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(19): Show | 50 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.631+972G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669384 | ||||||
chr19:48669384
|
CCACCACC others(185): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.631+780_631+971del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669384 | ||||||
chr19:48669385
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631+971G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669385 | ||||||
chr19:48669387
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0071others(4): Show | 19 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.631+969G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669387 | ||||||
chr19:48669390
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0096others(1): Show | 10 | HG00099.hp1 HG04115.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+966G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669390 | ||||||
chr19:48669390
|
CCAT | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(20): Show | 71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.631+963_631+965del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669390 | ||||||
chr19:48669392
|
A | C | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+964T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669392 | ||||||
chr19:48669393
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0087others(4): Show | 19 | HG00099.hp1 HG01123.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.631+963A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669393 | ||||||
chr19:48669393
|
TCACCACC others(32): Show |
T | 1 | a0001c0002t0002g0143 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.631+924_631+962del others(39): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669393 | ||||||
chr19:48669396
|
C | CCAT | 19 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(16): Show | 45 | HG00408.hp1 HG00735.hp1 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.631+959_631+960ins others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669396 | ||||||
chr19:48669397
|
C | T | 1 | a0001c0001t0001g0012 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+959G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669397 | ||||||
chr19:48669399
|
C | A | 3 | a0001c0002t0002g0014a0001c0002t0002g0048a0001c0002t0002g0135 | 9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+957G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669399 | ||||||
chr19:48669399
|
C | T | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0065others(5): Show | 8 | HG00735.hp1 HG02293.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+957G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669399 | ||||||
chr19:48669402
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0017others(19): Show | 76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.631+954G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669402 | ||||||
chr19:48669405
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(20): Show | 52 | HG00099.hp1 HG00621.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.631+951G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669405 | ||||||
chr19:48669407
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+949T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669407 | ||||||
chr19:48669408
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+948A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669408 | ||||||
chr19:48669408
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 13 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.631+948A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669408 | ||||||
chr19:48669411
|
C | G | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+945G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669411 | ||||||
chr19:48669411
|
C | T | 5 | a0001c0002t0002g0014a0001c0002t0002g0048a0001c0002t0002g0135others(2): Show | 11 | HG01123.hp2 HG01257.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.631+945G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669411 | ||||||
chr19:48669412
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+944G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669412 | ||||||
chr19:48669414
|
C | CCACCATC others(133): Show |
1 | a0001c0002t0002g0052 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.631+941_631+942ins others(140): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | ||||||
chr19:48669414
|
C | CCACCATC others(2): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00735.hp1 HG02293.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+941_631+942ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | ||||||
chr19:48669414
|
C | CCATCACC others(74): Show |
1 | a0001c0001t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.631+941_631+942ins others(81): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | ||||||
chr19:48669414
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(18): Show | 50 | HG00544.hp1 HG00621.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.631+942G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | ||||||
chr19:48669416
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+940T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669416 | ||||||
chr19:48669417
|
C | T | 3 | a0001c0002t0002g0014a0001c0002t0002g0048a0001c0002t0002g0135 | 9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+939G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669417 | ||||||
chr19:48669419
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+937T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669419 | ||||||
chr19:48669420
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+936A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669420 | ||||||
chr19:48669420
|
T | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(16): Show | 47 | HG00597.hp2 HG00621.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.631+936A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669420 | ||||||
chr19:48669420
|
TCAC | T | 2 | a0001c0003t0001g0023a0001c0003t0001g0053 | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+933_631+935del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669420 | ||||||
chr19:48669423
|
C | T | 4 | a0001c0001t0001g0087a0001c0002t0001g0034a0001c0002t0002g0146others(1): Show | 5 | HG01261.hp1 HG01891.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.631+933G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669423 | ||||||
chr19:48669426
|
C | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(14): Show | 45 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.631+930G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669426 | ||||||
chr19:48669426
|
C | T | 20 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0017others(17): Show | 73 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.631+930G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669426 | ||||||
chr19:48669429
|
T | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(20): Show | 52 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.631+927A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669429 | ||||||
chr19:48669432
|
C | CCACCACC others(2): Show |
1 | a0001c0001t0001g0012 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+923_631+924ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669432 | ||||||
chr19:48669432
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631+924G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669432 | ||||||
chr19:48669435
|
C | A | 2 | a0001c0002t0002g0134a0001c0002t0002g0151 | 2 | HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.631+921G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | ||||||
chr19:48669435
|
C | CTACCATC others(34): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0041others(4): Show | 40 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.631+920_631+921ins others(41): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | ||||||
chr19:48669435
|
C | CTACCATC others(55): Show |
1 | a0001c0001t0001g0018 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+920_631+921ins others(62): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | ||||||
chr19:48669435
|
C | CTACCATC others(79): Show |
1 | a0001c0002t0002g0136 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.631+920_631+921ins others(86): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | ||||||
chr19:48669435
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(19): Show | 58 | HG00408.hp1 HG01243.hp1 HG01258.hp1 others(55): Show |
intron_variant | MODIFIER | c.631+921G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | ||||||
chr19:48669436
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0011others(7): Show | 21 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.631+920G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669436 | ||||||
chr19:48669437
|
AC | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(12): Show | 41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+918delG | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669437 | ||||||
chr19:48669438
|
C | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(16): Show | 47 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.631+918G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669438 | ||||||
chr19:48669438
|
CCACCACC others(131): Show |
C | 1 | a0001c0001t0001g0065 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.631+780_631+917del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669438 | ||||||
chr19:48669439
|
C | G | 1 | a0001c0002t0002g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.631+917G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669439 | ||||||
chr19:48669441
|
C | T | 13 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0002t0002g0011others(10): Show | 30 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.631+915G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669441 | ||||||
chr19:48669441
|
CCACCATC others(65): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631+843_631+914del others(72): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669441 | ||||||
chr19:48669441
|
CCACCATC others(128): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.631+780_631+914del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669441 | ||||||
chr19:48669444
|
C | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(20): Show | 55 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.631+912G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669444 | ||||||
chr19:48669446
|
ATCACCAC others(283): Show |
A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+620_631+909del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669446 | ||||||
chr19:48669447
|
T | A | 1 | a0001c0001t0001g0018 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+909A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669447 | ||||||
chr19:48669447
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(12): Show | 41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+909A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669447 | ||||||
chr19:48669447
|
TCACCACC others(65): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631+837_631+908del others(72): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669447 | ||||||
chr19:48669448
|
C | CACACCAC others(61): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.631+907_631+908ins others(68): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669448 | ||||||
chr19:48669448
|
C | G | 4 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(1): Show | 14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+908G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669448 | ||||||
chr19:48669450
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(20): Show | 82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.631+906G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669450 | ||||||
chr19:48669450
|
CCACCATG | C | 8 | a0001c0002t0002g0011a0001c0002t0002g0032a0001c0002t0002g0138others(5): Show | 19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+899_631+905del others(7): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669450 | ||||||
chr19:48669451
|
CACCATG | C | 2 | a0001c0003t0001g0023a0001c0003t0001g0053 | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+899_631+904del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669451 | ||||||
chr19:48669453
|
C | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0059a0001c0001t0001g0075others(10): Show | 20 | HG00099.hp1 HG00735.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.631+903G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669453 | ||||||
chr19:48669453
|
CCATGACC others(5): Show |
C | 3 | a0001c0002t0002g0014a0001c0002t0002g0048a0001c0002t0002g0135 | 9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+891_631+902del others(12): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669453 | ||||||
chr19:48669456
|
T | C | 11 | a0001c0001t0001g0018a0001c0001t0001g0059a0001c0001t0001g0075others(8): Show | 15 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.631+900A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669456 | ||||||
chr19:48669456
|
T | TCACCAC | 4 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(1): Show | 14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+899_631+900ins others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669456 | ||||||
chr19:48669457
|
G | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(58): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.631+899C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669457 | ||||||
chr19:48669459
|
C | T | 1 | a0001c0001t0001g0018 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+897G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669459 | ||||||
chr19:48669463
|
C | T | 1 | a0001c0002t0002g0136 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.631+893G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669463 | ||||||
chr19:48669465
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631+891A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669465 | ||||||
chr19:48669465
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 108 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.631+891A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669465 | ||||||
chr19:48669468
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0041others(4): Show | 40 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.631+888A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669468 | ||||||
chr19:48669468
|
T | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0059a0001c0001t0001g0075others(13): Show | 27 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.631+888A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669468 | ||||||
chr19:48669468
|
TCAC | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(12): Show | 41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+885_631+887del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669468 | ||||||
chr19:48669471
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(14): Show | 45 | HG01074.hp1 HG01074.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.631+885G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669471 | ||||||
chr19:48669472
|
C | A | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+884G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669472 | ||||||
chr19:48669473
|
A | G | 1 | a0003c0006t0002g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+883T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669473 | ||||||
chr19:48669474
|
C | T | 9 | a0001c0002t0002g0011a0001c0002t0002g0032a0001c0002t0002g0136others(6): Show | 20 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.631+882G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669474 | ||||||
chr19:48669477
|
T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0041others(22): Show | 79 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.631+879A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669477 | ||||||
chr19:48669480
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0017others(7): Show | 53 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.631+876G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669480 | ||||||
chr19:48669483
|
C | T | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0087others(10): Show | 24 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.631+873G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669483 | ||||||
chr19:48669486
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0028others(23): Show | 69 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.631+870A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669486 | ||||||
chr19:48669486
|
T | TCAC | 2 | a0001c0001t0001g0012a0001c0001t0001g0087 | 8 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+867_631+869dup others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669486 | ||||||
chr19:48669489
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0041others(8): Show | 54 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+867G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669489 | ||||||
chr19:48669492
|
T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.631+864A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669492 | ||||||
chr19:48669495
|
C | CACCACCA others(28): Show |
1 | a0001c0001t0001g0059 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.631+860_631+861ins others(35): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669495 | ||||||
chr19:48669495
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+861G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669495 | ||||||
chr19:48669498
|
C | CCACCACC others(92): Show |
1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.631+857_631+858ins others(99): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669498 | ||||||
chr19:48669498
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(24): Show | 99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.631+858G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669498 | ||||||
chr19:48669501
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+855G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669501 | ||||||
chr19:48669502
|
CACG | C | 1 | a0001c0001t0001g0018 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+851_631+853del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669502 | ||||||
chr19:48669504
|
C | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(16): Show | 53 | HG01074.hp1 HG01074.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.631+852G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669504 | ||||||
chr19:48669504
|
CGACCAT | C | 3 | a0001c0003t0001g0023a0001c0003t0001g0053a0008c0013t0002g0130 | 7 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+846_631+851del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669504 | ||||||
chr19:48669505
|
G | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(60): Show | 183 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.631+851C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669505 | ||||||
chr19:48669507
|
C | T | 8 | a0001c0001t0001g0087a0001c0002t0002g0011a0001c0002t0002g0032others(5): Show | 19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+849G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669507 | ||||||
chr19:48669508
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(12): Show | 41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+848G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669508 | ||||||
chr19:48669510
|
T | A | 4 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(1): Show | 14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+846A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | ||||||
chr19:48669510
|
T | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(27): Show | 68 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.631+846A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | ||||||
chr19:48669510
|
T | TCATCACC others(142): Show |
1 | a0001c0002t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+845_631+846ins others(149): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | ||||||
chr19:48669510
|
TCATCACC others(26): Show |
T | 15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(12): Show | 43 | HG01074.hp1 HG01074.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.631+813_631+845del others(33): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | ||||||
chr19:48669513
|
T | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0071others(10): Show | 32 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.631+843A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669513 | ||||||
chr19:48669513
|
TCAC | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(12): Show | 41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+840_631+842del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669513 | ||||||
chr19:48669513
|
TCACCACC others(201): Show |
T | 3 | a0001c0002t0002g0014a0001c0002t0002g0048a0001c0002t0002g0135 | 9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+635_631+842del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669513 | ||||||
chr19:48669516
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 13 | HG01978.hp2 HG01981.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.631+840G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669516 | ||||||
chr19:48669519
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0041others(7): Show | 43 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.631+837G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669519 | ||||||
chr19:48669522
|
C | T | 6 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0002t0002g0010others(3): Show | 16 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+834G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669522 | ||||||
chr19:48669523
|
C | T | 8 | a0001c0001t0001g0059a0001c0002t0002g0011a0001c0002t0002g0032others(5): Show | 19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+833G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669523 | ||||||
chr19:48669525
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0003t0001g0023others(1): Show | 8 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+831G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669525 | ||||||
chr19:48669528
|
T | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0075others(5): Show | 12 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.631+828A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669528 | ||||||
chr19:48669528
|
T | TCATCACC others(215): Show |
1 | a0001c0001t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.631+827_631+828ins others(222): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669528 | ||||||
chr19:48669531
|
C | T | 10 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0081others(7): Show | 21 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.631+825G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669531 | ||||||
chr19:48669534
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0028others(18): Show | 50 | HG00280.hp2 HG00408.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.631+822G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669534 | ||||||
chr19:48669537
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(14): Show | 43 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.631+819G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669537 | ||||||
chr19:48669540
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(25): Show | 90 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.631+816A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669540 | ||||||
chr19:48669543
|
C | CCACCACC others(134): Show |
1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+812_631+813ins others(141): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | ||||||
chr19:48669543
|
C | CCACCACC others(289): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.631+812_631+813ins others(296): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | ||||||
chr19:48669543
|
C | CCATCACC others(2): Show |
8 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0041others(5): Show | 41 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.631+812_631+813ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | ||||||
chr19:48669543
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631+813G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | ||||||
chr19:48669544
|
C | CACCATCA others(106): Show |
1 | a0001c0001t0001g0012 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+811_631+812ins others(113): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669544 | ||||||
chr19:48669544
|
C | CATCATCA others(5): Show |
8 | a0001c0001t0001g0059a0001c0002t0002g0011a0001c0002t0002g0032others(5): Show | 19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+811_631+812ins others(12): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669544 | ||||||
chr19:48669544
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(14): Show | 43 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.631+812G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669544 | ||||||
chr19:48669546
|
C | CCACCATC others(83): Show |
1 | a0001c0002t0002g0114 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.631+809_631+810ins others(90): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669546 | ||||||
chr19:48669546
|
C | CCACCATC others(44): Show |
1 | a0001c0001t0001g0100 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+809_631+810ins others(51): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669546 | ||||||
chr19:48669546
|
C | T | 1 | a0001c0001t0001g0018 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+810G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669546 | ||||||
chr19:48669549
|
C | CCATCATC others(71): Show |
1 | a0001c0002t0002g0052 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.631+806_631+807ins others(78): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | ||||||
chr19:48669549
|
C | CCATCATC others(32): Show |
1 | a0001c0001t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631+806_631+807ins others(39): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | ||||||
chr19:48669549
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(26): Show | 73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.631+807G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | ||||||
chr19:48669549
|
CCACCAT | C | 2 | a0001c0003t0001g0023a0001c0003t0001g0053 | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+801_631+806del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | ||||||
chr19:48669552
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0126a0001c0002t0002g0010others(3): Show | 16 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+804G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669552 | ||||||
chr19:48669555
|
T | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0075a0001c0002t0002g0052others(1): Show | 8 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+801A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669555 | ||||||
chr19:48669555
|
TCACCAC | T | 4 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(1): Show | 14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+795_631+800del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669555 | ||||||
chr19:48669558
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(15): Show | 67 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.631+798G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669558 | ||||||
chr19:48669558
|
CCACCACC others(11): Show |
C | 1 | a0001c0015t0001g0073 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.631+780_631+797del others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669558 | ||||||
chr19:48669565
|
C | T | 1 | a0001c0002t0002g0136 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.631+791G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669565 | ||||||
chr19:48669567
|
T | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0001g0034others(3): Show | 7 | HG01891.hp1 HG01978.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.631+789A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669567 | ||||||
chr19:48669568
|
C | G | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+788G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669568 | ||||||
chr19:48669570
|
C | T | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0100others(3): Show | 6 | HG01978.hp2 HG01981.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+786G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669570 | ||||||
chr19:48669573
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.631+783G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669573 | ||||||
chr19:48669573
|
CCATCACC others(105): Show |
C | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+671_631+782del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669573 | ||||||
chr19:48669575
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+781T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669575 | ||||||
chr19:48669576
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 145 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.631+780A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669576
|
T | TCACCACC others(2): Show |
13 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0002g0044others(10): Show | 41 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.631+771_631+779dup others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669576
|
T | TCACCACC others(269): Show |
1 | a0001c0002t0002g0115 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.631+779_631+780ins others(276): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669576
|
T | TCACCACC others(86): Show |
1 | a0001c0002t0002g0043 | 2 | HG00544.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.631+779_631+780ins others(93): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669576
|
T | TCACCACC others(353): Show |
1 | a0001c0002t0002g0030 | 3 | NA18960.hp1 NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.631+779_631+780ins others(360): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669576
|
T | TCACCACC others(386): Show |
1 | a0001c0002t0002g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.631+779_631+780ins others(393): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669576
|
T | TCACCATC others(2): Show |
36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.631+779_631+780ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | ||||||
chr19:48669582
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+774G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669582 | ||||||
chr19:48669583
|
C | T | 2 | a0001c0001t0001g0060a0001c0002t0002g0136 | 2 | HG02040.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.631+773G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669583 | ||||||
chr19:48669585
|
C | T | 3 | a0001c0001t0001g0127a0001c0002t0002g0134a0001c0002t0002g0151 | 3 | HG00733.hp2 HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.631+771G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669585 | ||||||
chr19:48669586
|
G | C | 18 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072others(15): Show | 29 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.631+770C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669586 | ||||||
chr19:48669588
|
C | T | 2 | a0001c0001t0001g0060a0001c0002t0002g0136 | 2 | HG02040.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.631+768G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669588 | ||||||
chr19:48669591
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+765G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669591 | ||||||
chr19:48669594
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+762A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669594 | ||||||
chr19:48669597
|
CCACCACC others(176): Show |
C | 2 | a0001c0002t0002g0134a0001c0002t0002g0151 | 2 | HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.631+576_631+758del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669597 | ||||||
chr19:48669600
|
C | T | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+756G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669600 | ||||||
chr19:48669603
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+753G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669603 | ||||||
chr19:48669609
|
T | C | 6 | a0001c0001t0001g0126a0001c0002t0001g0034a0001c0002t0002g0010others(3): Show | 17 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+747A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669609 | ||||||
chr19:48669615
|
C | T | 2 | a0001c0001t0001g0100a0001c0002t0001g0034 | 3 | HG01891.hp1 HG02293.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+741G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669615 | ||||||
chr19:48669618
|
C | T | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+738G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669618 | ||||||
chr19:48669628
|
C | T | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+728G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669628 | ||||||
chr19:48669630
|
CCAGT | C | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+722_631+725del others(4): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669630 | ||||||
chr19:48669632
|
AG | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.631+723delC | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669632 | ||||||
chr19:48669633
|
G | A | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+723C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669633 | ||||||
chr19:48669634
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0001g0034 | 4 | HG01891.hp1 HG06807.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+722A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669634 | ||||||
chr19:48669644
|
CACCACCA others(3): Show |
C | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+702_631+711del others(10): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669644 | ||||||
chr19:48669646
|
C | T | 1 | a0001c0002t0001g0034 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+710G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669646 | ||||||
chr19:48669655
|
A | C | 2 | a0001c0001t0001g0100a0001c0004t0001g0106 | 2 | HG02293.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.631+701T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669655 | ||||||
chr19:48669655
|
A | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0001g0034 | 4 | HG01891.hp1 HG06807.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+701T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669655 | ||||||
chr19:48669661
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+695G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669661 | ||||||
chr19:48669667
|
T | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(14): Show | 58 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.631+689A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669667 | ||||||
chr19:48669673
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0001g0034 | 4 | HG01891.hp1 HG06807.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+683A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669673 | ||||||
chr19:48669676
|
T | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072others(6): Show | 20 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.631+680A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669676 | ||||||
chr19:48669679
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+677G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669679 | ||||||
chr19:48669680
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+676G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669680 | ||||||
chr19:48669682
|
C | T | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+674G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669682 | ||||||
chr19:48669688
|
CCACCACC others(2): Show |
C | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+659_631+667del others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669688 | ||||||
chr19:48669691
|
C | T | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+665G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669691 | ||||||
chr19:48669694
|
CCAT | C | 26 | a0001c0001t0001g0149a0001c0001t0002g0145a0001c0002t0001g0109others(23): Show | 70 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.631+659_631+661del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669694 | ||||||
chr19:48669697
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+659A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669697 | ||||||
chr19:48669706
|
T | C | 7 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0126others(4): Show | 17 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+650A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669706 | ||||||
chr19:48669710
|
C | T | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+646G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669710 | ||||||
chr19:48669712
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+644G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669712 | ||||||
chr19:48669715
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02040.hp1 NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+641A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669715 | ||||||
chr19:48669721
|
C | CCACCACC others(11): Show |
4 | a0001c0003t0001g0022a0001c0003t0001g0023a0001c0003t0001g0053others(1): Show | 11 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.631+617_631+634dup others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669721 | ||||||
chr19:48669721
|
C | T | 6 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(3): Show | 16 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+635G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669721 | ||||||
chr19:48669724
|
C | CCACCACC others(2): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0061others(4): Show | 27 | NA18939.hp2 NA18944.hp2 NA18945.hp1 others(24): Show |
intron_variant | MODIFIER | c.631+623_631+631dup others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669724 | ||||||
chr19:48669724
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02040.hp1 NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+632G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669724 | ||||||
chr19:48669730
|
CCAT | C | 5 | a0001c0001t0001g0126a0001c0002t0002g0010a0001c0002t0002g0046others(2): Show | 15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+623_631+625del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669730 | ||||||
chr19:48669733
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02040.hp1 NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+623A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669733 | ||||||
chr19:48669734
|
C | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0126a0001c0002t0002g0010others(3): Show | 16 | HG01243.hp1 HG01884.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+622G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669734 | ||||||
chr19:48669742
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+614G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669742 | ||||||
chr19:48669749
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+607G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669749 | ||||||
chr19:48669750
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+606T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669750 | ||||||
chr19:48669751
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+605A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669751 | ||||||
chr19:48669754
|
CCATCGTC others(19): Show |
C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+576_631+601del others(26): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669754 | ||||||
chr19:48669759
|
G | A | 47 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0126others(44): Show | 115 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.631+597C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669759 | ||||||
chr19:48669760
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+596A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669760 | ||||||
chr19:48669767
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+589A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669767 | ||||||
chr19:48669768
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+588T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669768 | ||||||
chr19:48669771
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+585T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669771 | ||||||
chr19:48669772
|
TCACCATC others(40): Show |
T | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+537_631+583del others(47): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669772 | ||||||
chr19:48669776
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.631+580G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669776 | ||||||
chr19:48669789
|
C | T | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+567G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669789 | ||||||
chr19:48669792
|
T | C | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+564A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669792 | ||||||
chr19:48669795
|
C | T | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+561G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669795 | ||||||
chr19:48669807
|
T | C | 2 | a0001c0002t0002g0131a0008c0013t0002g0130 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+549A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669807 | ||||||
chr19:48669810
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | NA18942.hp2 NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+546A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669810 | ||||||
chr19:48669812
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+544T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669812 | ||||||
chr19:48669816
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+540A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669816 | ||||||
chr19:48669819
|
C | CCACCACC others(47): Show |
1 | a0001c0001t0001g0074 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.631+483_631+536dup others(54): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669819 | ||||||
chr19:48669819
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+537G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669819 | ||||||
chr19:48669825
|
C | T | 5 | a0001c0001t0001g0055a0001c0002t0001g0054a0001c0002t0001g0153others(2): Show | 8 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+531G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669825 | ||||||
chr19:48669826
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+530G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669826 | ||||||
chr19:48669831
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+525A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669831 | ||||||
chr19:48669835
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+521G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669835 | ||||||
chr19:48669836
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+520T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669836 | ||||||
chr19:48669837
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.631+519A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669837 | ||||||
chr19:48669840
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+516G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669840 | ||||||
chr19:48669845
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+511T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669845 | ||||||
chr19:48669846
|
C | T | 1 | a0008c0013t0002g0130 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+510G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669846 | ||||||
chr19:48669847
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+509A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669847 | ||||||
chr19:48669847
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0002g0131others(1): Show | 4 | HG02615.hp1 HG03139.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+509A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669847 | ||||||
chr19:48669848
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+508T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669848 | ||||||
chr19:48669849
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+507G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669849 | ||||||
chr19:48669849
|
C | T | 2 | a0001c0002t0002g0131a0008c0013t0002g0130 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+507G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669849 | ||||||
chr19:48669852
|
T | C | 2 | a0001c0002t0002g0131a0008c0013t0002g0130 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+504A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669852 | ||||||
chr19:48669855
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+501G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669855 | ||||||
chr19:48669858
|
CCACCATC others(20): Show |
C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+471_631+497del others(27): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669858 | ||||||
chr19:48669868
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+488G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669868 | ||||||
chr19:48669869
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+487T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669869 | ||||||
chr19:48669870
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+486A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669870 | ||||||
chr19:48669873
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+483A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669873 | ||||||
chr19:48669879
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+477G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669879 | ||||||
chr19:48669880
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+476A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669880 | ||||||
chr19:48669881
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+475T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669881 | ||||||
chr19:48669891
|
T | C | 1 | a0001c0001t0001g0016 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+465A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669891 | ||||||
chr19:48669891
|
T | TCACCAC | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01168.hp2 HG01993.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.631+459_631+464dup others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669891 | ||||||
chr19:48669897
|
C | T | 1 | a0001c0001t0001g0016 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+459G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669897 | ||||||
chr19:48669900
|
C | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0002g0010others(2): Show | 15 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.631+456G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669900 | ||||||
chr19:48669903
|
T | TCATCACC others(5): Show |
1 | a0001c0001t0001g0016 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+452_631+453ins others(12): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669903 | ||||||
chr19:48669906
|
C | T | 1 | a0001c0001t0001g0016 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+450G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669906 | ||||||
chr19:48669909
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+447G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669909 | ||||||
chr19:48669913
|
C | CACCATCA others(14): Show |
1 | a0001c0015t0001g0073 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.631+422_631+442dup others(21): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669913 | ||||||
chr19:48669918
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+438A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669918 | ||||||
chr19:48669947
|
ACCACCAC others(30): Show |
A | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(15): Show | 58 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.631+372_631+408del others(37): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669947 | ||||||
chr19:48669952
|
CACCATCA others(33): Show |
C | 1 | a0001c0001t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+364_631+403del others(40): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669952 | ||||||
chr19:48669954
|
CCATCACC others(11): Show |
C | 1 | a0001c0001t0001g0059 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.631+384_631+401del others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669954 | ||||||
chr19:48669960
|
C | CCAT | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(111): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.631+393_631+395dup others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669960 | ||||||
chr19:48669963
|
T | C | 1 | a0001c0001t0001g0016 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+393A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669963 | ||||||
chr19:48669966
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+390G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669966 | ||||||
chr19:48669972
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(112): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.631+384A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669972 | ||||||
chr19:48669972
|
T | TCACCATC others(11): Show |
1 | a0001c0001t0001g0016 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+383_631+384ins others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669972 | ||||||
chr19:48669983
|
AT | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(112): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.631+372delA | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669983 | ||||||
chr19:48669990
|
C | CTACCATC others(8): Show |
1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+365_631+366ins others(15): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669990 | ||||||
chr19:48669996
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+360A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669996 | ||||||
chr19:48670002
|
TCACCACC others(8): Show |
T | 1 | a0001c0002t0002g0047 | 2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.631+339_631+353del others(15): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48670002 | ||||||
chr19:48670026
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.631+330A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48670026 | ||||||
chr19:48671017
|
G | A | 1 | a0001c0002t0002g0031 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20-11C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671017 | ||||||
chr19:48671035
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-29C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671035 | ||||||
chr19:48671275
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20-269C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671275 | ||||||
chr19:48671478
|
A | G | 58 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0126others(55): Show | 141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-472T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671478 | ||||||
chr19:48671642
|
G | A | 1 | a0001c0002t0002g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-20-636C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671642 | ||||||
chr19:48672012
|
C | T | 5 | a0001c0002t0002g0015a0001c0002t0002g0128a0001c0002t0002g0129others(2): Show | 9 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+920G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672012 | ||||||
chr19:48672094
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(68): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-21+838G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672094 | ||||||
chr19:48672151
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0057 | 3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-21+781G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672151 | ||||||
chr19:48672353
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-21+579C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672353 | ||||||
chr19:48672429
|
C | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0002g0010others(2): Show | 15 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+503G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672429 | ||||||
chr19:48672496
|
A | G | 2 | a0001c0002t0002g0013a0001c0002t0002g0031 | 9 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+436T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672496 | ||||||
chr19:48672642
|
CTT | C | 47 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0149others(44): Show | 118 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-21+288_-21+289del others(2): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672642 | ||||||
chr19:48672707
|
G | C | 8 | a0001c0001t0001g0055a0001c0002t0001g0054a0001c0002t0001g0153others(5): Show | 17 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21+225C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672707 | ||||||
chr19:48672778
|
C | G | 1 | a0001c0002t0002g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-21+154G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672778 | ||||||
chr19:48672909
|
T | C | 2 | a0001c0002t0002g0155a0001c0002t0002g0156 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-21+23A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672909 |