geneid | 53371 |
---|---|
ensemblid | ENSG00000138750.16 |
hgncid | 17359 |
symbol | NUP54 |
name | nucleoporin 54 |
refseq_nuc | NM_017426.4 |
refseq_prot | NP_059122.2 |
ensembl_nuc | ENST00000264883.8 |
ensembl_prot | ENSP00000264883.3 |
mane_status | MANE Select |
chr | chr4 |
start | 76114664 |
end | 76148397 |
strand | - |
ver | v1.2 |
region | chr4:76114664-76148397 |
region5000 | chr4:76109664-76153397 |
regionname0 | NUP54_chr4_76114664_76148397 |
regionname5000 | NUP54_chr4_76109664_76153397 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 507 | 240 | 57 | 43 | 103 | 12 | 23 | 80 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0002 | 0/0 | 508 | 85 | 5 | 12 | 61 | 1 | 6 | 46 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0003 | 0/0 | 507 | 43 | 22 | 13 | 3 | 3 | 2 | 3 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0004 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0005 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1524 | 214 | 45 | 43 | 89 | 12 | 23 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0002 | 0/0 | 1527 | 85 | 5 | 12 | 61 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0003 | 0/0 | 1524 | 39 | 18 | 13 | 3 | 3 | 2 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0004 | 0/0 | 1524 | 25 | 11 | 0 | 14 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0005 | 0/0 | 1524 | 4 | 4 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0006 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0007 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 726 | 98 | 27 | 27 | 23 | 10 | 9 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0002 | 0/0 | 726 | 98 | 37 | 15 | 33 | 4 | 9 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0003 | 0/0 | 726 | 87 | 5 | 12 | 62 | 1 | 7 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0004 | 0/0 | 722 | 77 | 7 | 13 | 50 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0005 | 0/0 | 726 | 7 | 6 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0006 | 0/0 | 726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0007 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
t0008 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0010 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1524 | 214 | 45 | 43 | 89 | 12 | 23 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0004 | 0/0 | 1524 | 25 | 11 | 0 | 14 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0002c0002 | 0/0 | 1527 | 85 | 5 | 12 | 61 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0003c0003 | 0/0 | 1524 | 39 | 18 | 13 | 3 | 3 | 2 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0003c0005 | 0/0 | 1524 | 4 | 4 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0004c0006 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0005c0007 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2249 | 37 | 1 | 14 | 6 | 7 | 7 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0001t0002 | 0/0 | 2249 | 98 | 37 | 15 | 33 | 4 | 9 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0001t0004 | 0/0 | 2245 | 70 | 0 | 13 | 50 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0001t0005 | 0/0 | 2249 | 6 | 5 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0001t0006 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0001t0007 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0001t0008 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0004t0001 | 0/0 | 2249 | 18 | 4 | 0 | 14 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0004t0004 | 0/0 | 2245 | 7 | 7 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0001c0008t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0002c0002t0003 | 0/0 | 2252 | 85 | 5 | 12 | 61 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0003c0003t0001 | 0/0 | 2249 | 39 | 18 | 13 | 3 | 3 | 2 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0003c0005t0001 | 0/0 | 2249 | 4 | 4 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0004c0006t0003 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
a0005c0007t0003 | 0/0 | 2252 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | copy fasta | chr4 | 76109664 | 76153397 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0010 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0004t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0001c0008t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0001 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0005t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0005t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0003c0005t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0004c0006t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
a0005c0007t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0229 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00140 | hp1 | a0003 | c0003 | t0001 | g0275 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00423 | hp1 | a0002 | c0002 | t0003 | g0072 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00558 | hp2 | a0002 | c0002 | t0003 | g0065 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00597 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00609 | hp1 | a0002 | c0002 | t0003 | g0080 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0326 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00673 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0270 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0280 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0273 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01099 | hp2 | a0002 | c0002 | t0003 | g0032 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01106 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0278 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0100 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0064 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01243 | hp2 | a0002 | c0002 | t0003 | g0046 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0265 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0291 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01261 | hp1 | a0002 | c0002 | t0003 | g0027 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01346 | hp2 | a0002 | c0002 | t0003 | g0013 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0297 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0242 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0294 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01516 | hp1 | a0003 | c0003 | t0001 | g0274 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01884 | hp1 | a0003 | c0005 | t0001 | g0312 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0037 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01934 | hp2 | a0002 | c0002 | t0003 | g0043 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01975 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01978 | hp1 | a0002 | c0002 | t0003 | g0045 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0102 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0292 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0298 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02015 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02027 | hp1 | a0002 | c0002 | t0003 | g0069 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02040 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02055 | hp1 | a0002 | c0002 | t0003 | g0042 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02055 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02071 | hp1 | a0002 | c0002 | t0003 | g0041 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02080 | hp1 | a0002 | c0002 | t0003 | g0062 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02083 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02129 | hp2 | a0002 | c0002 | t0003 | g0074 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02145 | hp2 | a0003 | c0005 | t0001 | g0310 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0288 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0296 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02155 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0268 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02280 | hp1 | a0001 | c0004 | t0004 | g0306 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0277 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02572 | hp1 | a0003 | c0003 | t0001 | g0279 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0290 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0238 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0272 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0276 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0283 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0241 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0034 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02818 | hp1 | a0001 | c0008 | t0005 | g0304 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0266 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0239 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0311 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0231 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0067 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02970 | hp1 | a0003 | c0003 | t0001 | g0240 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0281 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0317 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03041 | hp2 | a0003 | c0005 | t0001 | g0313 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03130 | hp1 | a0001 | c0004 | t0004 | g0305 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0282 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03195 | hp2 | a0001 | c0004 | t0004 | g0308 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0109 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03516 | hp2 | a0003 | c0003 | t0001 | g0237 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03540 | hp1 | a0001 | c0004 | t0004 | g0302 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0267 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0156 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0143 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0039 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0068 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0035 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0295 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0098 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03927 | hp2 | a0002 | c0002 | t0003 | g0033 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04184 | hp1 | a0005 | c0007 | t0003 | g0066 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0075 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0108 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0284 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18522 | hp2 | a0001 | c0004 | t0004 | g0303 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18747 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18906 | hp2 | a0001 | c0004 | t0001 | g0315 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18939 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18940 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18942 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18943 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18945 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18946 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18948 | hp1 | a0001 | c0004 | t0001 | g0319 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18953 | hp1 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18957 | hp1 | a0002 | c0002 | t0003 | g0061 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18960 | hp1 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18960 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18962 | hp2 | a0001 | c0004 | t0001 | g0320 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18963 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18964 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18965 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18966 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18966 | hp2 | a0001 | c0004 | t0001 | g0321 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18969 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18970 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18972 | hp1 | a0002 | c0002 | t0003 | g0081 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18974 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18974 | hp2 | a0001 | c0004 | t0001 | g0325 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18977 | hp2 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18979 | hp1 | a0004 | c0006 | t0003 | g0031 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18980 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18981 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18984 | hp2 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18989 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18990 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18991 | hp1 | a0001 | c0004 | t0001 | g0316 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18991 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18992 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18994 | hp1 | a0001 | c0004 | t0001 | g0314 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18994 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA18999 | hp2 | a0001 | c0004 | t0001 | g0318 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0289 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19003 | hp2 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19009 | hp2 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19010 | hp2 | a0001 | c0004 | t0001 | g0327 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0324 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19043 | hp1 | a0001 | c0004 | t0004 | g0307 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19062 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19064 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19074 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19076 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19077 | hp1 | a0002 | c0002 | t0003 | g0036 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19077 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19078 | hp2 | a0001 | c0004 | t0001 | g0323 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19081 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19084 | hp2 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0322 | AFR | ASW | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ASW | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA20752 | hp1 | a0002 | c0002 | t0003 | g0063 | EUR | TSI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0236 | EUR | TSI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02109 | hp1 | a0003 | c0003 | t0001 | g0286 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG03471 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA21309 | hp1 | a0001 | c0004 | t0004 | g0309 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0257 | REF | REF | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0010 | REF | REF | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76132681
|
T | C | 1 | a0003 | 43 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(40): Show |
missense_variant | MODERATE | c.749A>G | p.Asn250Ser | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/12 | 772/2249 | 749/1524 | 250/507 | chr4 | 76132681 | ||
chr4:76144165
|
C | CTGT | 3 | a0002a0004a0005 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
disruptive_inframe_insertion | MODERATE | c.276_278dupACA | p.Gln93dup | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/12 | 301/2249 | 278/1524 | 93/507 | chr4 | 76144165 | ||
chr4:76144239
|
T | G | 1 | a0005 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.205A>C | p.Thr69Pro | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/12 | 228/2249 | 205/1524 | 69/507 | chr4 | 76144239 | ||
chr4:76144473
|
C | G | 1 | a0004 | 1 | NA18979.hp1 | missense_variant&splice_region_variant | MODERATE | c.68G>C | p.Gly23Ala | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/12 | 91/2249 | 68/1524 | 23/507 | chr4 | 76144473 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76132650
|
C | T | 1 | a0001c0008 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.780G>A | p.Thr260Thr | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/12 | 803/2249 | 780/1524 | 260/507 | chr4 | 76132650 | ||
chr4:76134321
|
A | G | 3 | a0002c0002a0004c0006a0005c0007 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.564T>C | p.Asp188Asp | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/12 | 587/2249 | 564/1524 | 188/507 | chr4 | 76134321 | ||
chr4:76136348
|
A | G | 3 | a0002c0002a0004c0006a0005c0007 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.360T>C | p.Thr120Thr | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/12 | 383/2249 | 360/1524 | 120/507 | chr4 | 76136348 | ||
chr4:76144427
|
T | C | 3 | a0002c0002a0004c0006a0005c0007 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.114A>G | p.Ala38Ala | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/12 | 137/2249 | 114/1524 | 38/507 | chr4 | 76144427 | ||
chr4:76148321
|
G | A | 3 | a0001c0004a0001c0008a0003c0005 | 30 | HG00673.hp1 HG01884.hp1 HG02083.hp1 others(27): Show |
synonymous_variant | LOW | c.54C>T | p.Thr18Thr | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/12 | 77/2249 | 54/1524 | 18/507 | chr4 | 76148321 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76114729
|
A | T | 1 | a0001c0001t0008 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 637 | chr4 | 76114729 | |||||
chr4:76114742
|
T | A | 3 | a0002c0002t0003a0004c0006t0003a0005c0007t0003 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*624A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 624 | chr4 | 76114742 | |||||
chr4:76114754
|
TTAAG | T | 2 | a0001c0001t0004a0001c0004t0004 | 77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*608_*611delCTTA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 608 | chr4 | 76114754 | |||||
chr4:76114761
|
G | A | 3 | a0002c0002t0003a0004c0006t0003a0005c0007t0003 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 605 | chr4 | 76114761 | |||||
chr4:76114892
|
C | T | 1 | a0001c0001t0006 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 474 | chr4 | 76114892 | |||||
chr4:76114929
|
A | C | 1 | a0001c0001t0007 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 437 | chr4 | 76114929 | |||||
chr4:76114969
|
T | C | 3 | a0001c0001t0002a0001c0001t0007a0001c0001t0008 | 100 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 397 | chr4 | 76114969 | |||||
chr4:76114975
|
G | C | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(7): Show | 271 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*391C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 391 | chr4 | 76114975 | |||||
chr4:76115216
|
G | A | 3 | a0002c0002t0003a0004c0006t0003a0005c0007t0003 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 150 | chr4 | 76115216 | |||||
chr4:76115253
|
T | G | 3 | a0002c0002t0003a0004c0006t0003a0005c0007t0003 | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*113A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 113 | chr4 | 76115253 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76115526
|
T | A | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-32A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115526 | ||||||
chr4:76115591
|
C | G | 1 | a0001c0001t0004g0227 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1396-97G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115591 | ||||||
chr4:76115683
|
T | A | 3 | a0003c0003t0001g0237a0003c0003t0001g0271a0003c0003t0001g0282 | 3 | HG03130.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1396-189A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115683 | ||||||
chr4:76115858
|
T | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1396-364A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115858 | ||||||
chr4:76115878
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1396-384C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115878 | ||||||
chr4:76115892
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1396-398A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115892 | ||||||
chr4:76116125
|
A | T | 1 | a0002c0002t0003g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1396-631T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116125 | ||||||
chr4:76116372
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1396-878A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116372 | ||||||
chr4:76116476
|
T | C | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1396-982A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116476 | ||||||
chr4:76116629
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+1035T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116629 | ||||||
chr4:76116693
|
C | T | 1 | a0003c0003t0001g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1395+971G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116693 | ||||||
chr4:76116807
|
G | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 5 | HG00738.hp1 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+857C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116807 | ||||||
chr4:76117016
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+648G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117016 | ||||||
chr4:76117022
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+642G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117022 | ||||||
chr4:76117023
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+641G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117023 | ||||||
chr4:76117027
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+637A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117027 | ||||||
chr4:76117030
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+634A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117030 | ||||||
chr4:76117031
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+633A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117031 | ||||||
chr4:76117033
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+631T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117033 | ||||||
chr4:76117040
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+624A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117040 | ||||||
chr4:76117292
|
C | A | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1395+372G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117292 | ||||||
chr4:76117320
|
T | C | 138 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(135): Show | 164 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.1395+344A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117320 | ||||||
chr4:76117417
|
C | T | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1395+247G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117417 | ||||||
chr4:76117421
|
C | G | 2 | a0003c0003t0001g0237a0003c0003t0001g0282 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1395+243G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117421 | ||||||
chr4:76117445
|
C | G | 3 | a0002c0002t0003g0032a0002c0002t0003g0039a0002c0002t0003g0040 | 3 | HG01099.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1395+219G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117445 | ||||||
chr4:76117446
|
C | T | 3 | a0002c0002t0003g0032a0002c0002t0003g0039a0002c0002t0003g0040 | 3 | HG01099.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1395+218G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117446 | ||||||
chr4:76117448
|
G | A | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1395+216C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117448 | ||||||
chr4:76117454
|
T | C | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1395+210A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117454 | ||||||
chr4:76117490
|
C | T | 72 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(69): Show | 77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1395+174G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117490 | ||||||
chr4:76117509
|
G | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+155C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117509 | ||||||
chr4:76117541
|
G | A | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1395+123C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117541 | ||||||
chr4:76117567
|
TCTCA | T | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0004t0004g0307 | 3 | HG01081.hp2 HG01258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1395+93_1395+96del others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117567 | ||||||
chr4:76117654
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+10G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117654 | ||||||
chr4:76117821
|
T | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1285-47A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76117821 | ||||||
chr4:76117903
|
C | T | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-129G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76117903 | ||||||
chr4:76118021
|
G | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1284+54C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76118021 | ||||||
chr4:76118028
|
G | T | 1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1284+47C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76118028 | ||||||
chr4:76118040
|
A | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1284+35T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76118040 | ||||||
chr4:76118198
|
T | C | 1 | a0003c0003t0001g0240 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.1165-4A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118198 | ||||||
chr4:76118199
|
A | G | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
splice_region_variant&intron_variant | LOW | c.1165-5T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118199 | ||||||
chr4:76118368
|
T | C | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1165-174A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118368 | ||||||
chr4:76118378
|
A | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-184T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118378 | ||||||
chr4:76118384
|
T | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-190A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118384 | ||||||
chr4:76118568
|
C | CGGGGGTG others(6): Show |
1 | a0001c0001t0002g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1165-375_1165-374i others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118568 | ||||||
chr4:76118568
|
C | T | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1165-374G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118568 | ||||||
chr4:76118569
|
G | GGGGGTGG others(3): Show |
1 | a0001c0001t0004g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1165-376_1165-375i others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118569 | ||||||
chr4:76118573
|
T | G | 2 | a0001c0001t0002g0299a0001c0001t0004g0133 | 2 | HG04115.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1165-379A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TG | 26 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(23): Show | 26 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1165-380dupC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TGGGGCGG others(2): Show |
35 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0082others(32): Show | 41 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TGGGGCGG others(3): Show |
41 | a0001c0001t0001g0253a0001c0001t0002g0017a0001c0001t0002g0018others(38): Show | 44 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TGGGGCGG others(4): Show |
23 | a0001c0001t0002g0148a0001c0001t0002g0150a0001c0001t0002g0158others(20): Show | 25 | HG00558.hp1 HG00639.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TGGGGCGG others(5): Show |
16 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0149others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TGGGGCGG others(6): Show |
6 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0004g0122others(3): Show | 6 | HG02165.hp2 HG02886.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
T | TGGGGCGG others(7): Show |
2 | a0001c0001t0002g0223a0001c0001t0004g0111 | 2 | HG02155.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1165-380_1165-379i others(16): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118573
|
TG | T | 73 | a0001c0001t0001g0230a0001c0001t0004g0014a0001c0001t0004g0115others(70): Show | 95 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1165-380delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | ||||||
chr4:76118577
|
G | GCGGGGGG others(3): Show |
1 | a0001c0001t0004g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1165-384_1165-383i others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118577 | ||||||
chr4:76118579
|
G | C | 2 | a0001c0001t0004g0115a0001c0001t0004g0118 | 2 | NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1165-385C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118579 | ||||||
chr4:76118583
|
G | T | 89 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(86): Show | 111 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1165-389C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118583 | ||||||
chr4:76118641
|
T | C | 70 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(67): Show | 91 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1165-447A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118641 | ||||||
chr4:76118727
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-533C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118727 | ||||||
chr4:76118734
|
G | A | 1 | a0001c0001t0004g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1165-540C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118734 | ||||||
chr4:76118747
|
G | A | 2 | a0001c0001t0004g0093a0001c0001t0004g0135 | 2 | NA19057.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1165-553C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118747 | ||||||
chr4:76118820
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-626A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118820 | ||||||
chr4:76118880
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1165-686G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118880 | ||||||
chr4:76118931
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1165-737C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118931 | ||||||
chr4:76118962
|
C | T | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-768G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118962 | ||||||
chr4:76119022
|
A | T | 72 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(69): Show | 77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1165-828T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119022 | ||||||
chr4:76119258
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1064C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119258 | ||||||
chr4:76119271
|
T | C | 230 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(227): Show | 265 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1165-1077A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119271 | ||||||
chr4:76119294
|
G | A | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165-1100C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119294 | ||||||
chr4:76119334
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1140A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119334 | ||||||
chr4:76119542
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1165-1348G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119542 | ||||||
chr4:76119542
|
CT | C | 176 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(173): Show | 193 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1165-1349delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119542 | ||||||
chr4:76119542
|
CTT | C | 67 | a0001c0001t0002g0082a0001c0001t0004g0133a0002c0002t0003g0001others(64): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1165-1350_1165-134 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119542 | ||||||
chr4:76119543
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1165-1349A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119543 | ||||||
chr4:76119658
|
G | A | 4 | a0002c0002t0003g0029a0002c0002t0003g0053a0002c0002t0003g0069others(1): Show | 4 | HG02027.hp1 HG02129.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-1464C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119658 | ||||||
chr4:76119677
|
T | C | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1165-1483A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119677 | ||||||
chr4:76119710
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-1516C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119710 | ||||||
chr4:76119773
|
G | A | 3 | a0002c0002t0003g0028a0002c0002t0003g0035a0002c0002t0003g0054 | 3 | HG03834.hp1 NA18960.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1165-1579C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119773 | ||||||
chr4:76119842
|
T | G | 1 | a0001c0004t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1165-1648A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119842 | ||||||
chr4:76119855
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1661G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119855 | ||||||
chr4:76119893
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1165-1699A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119893 | ||||||
chr4:76119910
|
A | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1716T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119910 | ||||||
chr4:76120083
|
A | G | 3 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086 | 3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1165-1889T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120083 | ||||||
chr4:76120099
|
C | T | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1165-1905G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120099 | ||||||
chr4:76120101
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1907G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120101 | ||||||
chr4:76120271
|
C | G | 1 | a0001c0001t0004g0127 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1165-2077G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120271 | ||||||
chr4:76120297
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2103A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120297 | ||||||
chr4:76120304
|
T | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2110A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120304 | ||||||
chr4:76120381
|
G | T | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1165-2187C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120381 | ||||||
chr4:76120401
|
G | A | 3 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086 | 3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1165-2207C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120401 | ||||||
chr4:76120421
|
CT | C | 48 | a0001c0001t0001g0244a0001c0004t0001g0004a0001c0004t0001g0314others(45): Show | 51 | HG00140.hp1 HG00673.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1165-2228delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | ||||||
chr4:76120421
|
CTTT | C | 9 | a0001c0001t0002g0184a0001c0001t0002g0199a0001c0001t0002g0200others(6): Show | 9 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1165-2230_1165-222 others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | ||||||
chr4:76120421
|
CTTTT | C | 150 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(147): Show | 164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1165-2231_1165-222 others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | ||||||
chr4:76120421
|
CTTTTT | C | 6 | a0001c0001t0002g0191a0001c0004t0004g0302a0001c0004t0004g0305others(3): Show | 6 | HG01515.hp2 HG02280.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-2232_1165-222 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | ||||||
chr4:76120427
|
T | C | 2 | a0001c0001t0005g0090a0001c0001t0005g0091 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1165-2233A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120427 | ||||||
chr4:76120443
|
T | C | 63 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(60): Show | 84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1165-2249A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120443 | ||||||
chr4:76120443
|
T | TC | 3 | a0002c0002t0003g0045a0002c0002t0003g0060a0002c0002t0003g0069 | 3 | HG01978.hp1 HG02027.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1165-2250_1165-224 others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120443 | ||||||
chr4:76120444
|
T | C | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1165-2250A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120444 | ||||||
chr4:76120459
|
G | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2265C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120459 | ||||||
chr4:76120465
|
T | C | 2 | a0003c0003t0001g0241a0003c0003t0001g0242 | 2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1165-2271A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120465 | ||||||
chr4:76120485
|
A | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2291T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120485 | ||||||
chr4:76120491
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2297C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120491 | ||||||
chr4:76120515
|
C | T | 5 | a0001c0001t0002g0189a0001c0001t0002g0192a0001c0001t0002g0194others(2): Show | 5 | HG02040.hp1 NA18940.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-2321G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120515 | ||||||
chr4:76120574
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2380T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120574 | ||||||
chr4:76120618
|
G | A | 64 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(61): Show | 69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1165-2424C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120618 | ||||||
chr4:76120635
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-2441C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120635 | ||||||
chr4:76120674
|
G | A | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165-2480C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120674 | ||||||
chr4:76120678
|
C | T | 3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1165-2484G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120678 | ||||||
chr4:76121370
|
G | T | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1165-3176C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121370 | ||||||
chr4:76121628
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+3021C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121628 | ||||||
chr4:76121636
|
T | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+3013A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121636 | ||||||
chr4:76121659
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1164+2990A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121659 | ||||||
chr4:76121938
|
TG | T | 4 | a0001c0001t0004g0095a0001c0001t0004g0119a0001c0001t0004g0129others(1): Show | 4 | HG00544.hp1 HG02027.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+2710delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121938 | ||||||
chr4:76121939
|
G | T | 1 | a0001c0001t0004g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1164+2710C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121939 | ||||||
chr4:76122004
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1164+2645A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122004 | ||||||
chr4:76122005
|
A | G | 1 | a0001c0004t0004g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1164+2644T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122005 | ||||||
chr4:76122060
|
G | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+2589C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122060 | ||||||
chr4:76122199
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1164+2450C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122199 | ||||||
chr4:76122297
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+2352A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122297 | ||||||
chr4:76122361
|
C | T | 7 | a0001c0001t0002g0016a0001c0001t0002g0152a0001c0001t0002g0153others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+2288G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122361 | ||||||
chr4:76122362
|
AC | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+2286delG | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122362 | ||||||
chr4:76122401
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1164+2248T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122401 | ||||||
chr4:76122450
|
C | A | 3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1164+2199G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122450 | ||||||
chr4:76122650
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1999A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122650 | ||||||
chr4:76122676
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1164+1973G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122676 | ||||||
chr4:76122708
|
T | C | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1164+1941A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122708 | ||||||
chr4:76122781
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1164+1868A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122781 | ||||||
chr4:76122789
|
A | G | 67 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(64): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1164+1860T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122789 | ||||||
chr4:76122792
|
G | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1857C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122792 | ||||||
chr4:76122794
|
G | GAACCACC others(3): Show |
1 | a0002c0002t0003g0030 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1164+1845_1164+185 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122794 | ||||||
chr4:76122808
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1841A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122808 | ||||||
chr4:76122826
|
T | C | 72 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(69): Show | 77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1164+1823A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122826 | ||||||
chr4:76122971
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+1678C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122971 | ||||||
chr4:76123084
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1565G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123084 | ||||||
chr4:76123105
|
C | T | 249 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(246): Show | 287 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.1164+1544G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123105 | ||||||
chr4:76123238
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1411G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123238 | ||||||
chr4:76123281
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1368G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123281 | ||||||
chr4:76123350
|
C | G | 1 | a0001c0001t0004g0020 | 2 | HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1164+1299G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123350 | ||||||
chr4:76123365
|
A | G | 64 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(61): Show | 69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1164+1284T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123365 | ||||||
chr4:76123387
|
T | C | 2 | a0001c0001t0004g0094a0001c0001t0004g0120 | 2 | NA18978.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1164+1262A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123387 | ||||||
chr4:76123450
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1199G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123450 | ||||||
chr4:76123653
|
C | T | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1164+996G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123653 | ||||||
chr4:76123658
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+991T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123658 | ||||||
chr4:76123803
|
T | C | 137 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(134): Show | 163 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1164+846A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123803 | ||||||
chr4:76123851
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+798C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123851 | ||||||
chr4:76124016
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1164+633A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124016 | ||||||
chr4:76124037
|
T | C | 1 | a0001c0001t0004g0136 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1164+612A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124037 | ||||||
chr4:76124441
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+208G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124441 | ||||||
chr4:76124575
|
A | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+74T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124575 | ||||||
chr4:76124583
|
ATATT | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+62_1164+65del others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124583 | ||||||
chr4:76124609
|
T | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+40A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124609 | ||||||
chr4:76124624
|
TGG | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+23_1164+24del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124624 | ||||||
chr4:76124629
|
G | C | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+20C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124629 | ||||||
chr4:76124783
|
A | G | 1 | a0001c0001t0004g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1057-27T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124783 | ||||||
chr4:76124784
|
G | A | 1 | a0001c0001t0004g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1057-28C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124784 | ||||||
chr4:76124832
|
TTCTAA | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-81_1057-77del others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124832 | ||||||
chr4:76124948
|
T | C | 1 | a0002c0002t0003g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1057-192A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124948 | ||||||
chr4:76124999
|
GA | G | 5 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-244delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124999 | ||||||
chr4:76125061
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-305T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125061 | ||||||
chr4:76125139
|
G | GA | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-384dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125139 | ||||||
chr4:76125258
|
CAACAGAG others(33): Show |
C | 12 | a0002c0002t0003g0002a0002c0002t0003g0005a0002c0002t0003g0030others(9): Show | 18 | HG00558.hp2 HG00673.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1057-542_1057-503d others(42): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125258 | ||||||
chr4:76125269
|
A | G | 54 | a0002c0002t0003g0001a0002c0002t0003g0006a0002c0002t0003g0007others(51): Show | 69 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1057-513T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125269 | ||||||
chr4:76125276
|
TCTCACAG others(37): Show |
T | 2 | a0002c0002t0003g0024a0002c0002t0003g0025 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1057-564_1057-521d others(46): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125276 | ||||||
chr4:76125276
|
TCTCACAG others(43): Show |
T | 1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1057-570_1057-521d others(52): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125276 | ||||||
chr4:76125278
|
T | A | 51 | a0002c0002t0003g0001a0002c0002t0003g0006a0002c0002t0003g0007others(48): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1057-522A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125278 | ||||||
chr4:76125280
|
ACAGAAAC others(29): Show |
A | 4 | a0002c0002t0003g0006a0002c0002t0003g0039a0002c0002t0003g0040others(1): Show | 6 | HG01069.hp1 HG01192.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-560_1057-525d others(38): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125280 | ||||||
chr4:76125282
|
AGAAACAA others(27): Show |
A | 30 | a0002c0002t0003g0007a0002c0002t0003g0011a0002c0002t0003g0013others(27): Show | 34 | HG00423.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1057-560_1057-527d others(36): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125282 | ||||||
chr4:76125283
|
G | C | 17 | a0002c0002t0003g0001a0002c0002t0003g0012a0002c0002t0003g0032others(14): Show | 26 | HG00597.hp2 HG01099.hp2 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.1057-527C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125283 | ||||||
chr4:76125283
|
GAAACAAA | G | 15 | a0001c0004t0001g0004a0001c0004t0001g0314a0001c0004t0001g0315others(12): Show | 18 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(15): Show |
intron_variant | MODIFIER | c.1057-534_1057-528d others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125283 | ||||||
chr4:76125284
|
AAACAAAA others(25): Show |
A | 15 | a0002c0002t0003g0001a0002c0002t0003g0012a0002c0002t0003g0032others(12): Show | 24 | HG00597.hp2 HG01099.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1057-560_1057-529d others(34): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125284 | ||||||
chr4:76125285
|
A | C | 2 | a0002c0002t0003g0044a0002c0002t0003g0075 | 2 | HG04199.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1057-529T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125285 | ||||||
chr4:76125286
|
ACAAAAAA others(23): Show |
A | 2 | a0002c0002t0003g0044a0002c0002t0003g0075 | 2 | HG04199.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1057-560_1057-531d others(32): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125286 | ||||||
chr4:76125316
|
T | TCA | 35 | a0001c0001t0001g0254a0001c0001t0002g0016a0001c0001t0002g0146others(32): Show | 36 | HG00544.hp1 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1057-562_1057-561d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | ||||||
chr4:76125316
|
T | TCACA | 10 | a0001c0001t0002g0153a0001c0001t0002g0165a0001c0001t0002g0218others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1057-564_1057-561d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | ||||||
chr4:76125316
|
T | TCACACAC others(3): Show |
3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1057-570_1057-561d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | ||||||
chr4:76125316
|
TCA | T | 86 | a0001c0001t0001g0021a0001c0001t0001g0234a0001c0001t0001g0247others(83): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1057-562_1057-561d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | ||||||
chr4:76125316
|
TCACA | T | 14 | a0001c0001t0005g0090a0001c0004t0001g0004a0001c0004t0001g0314others(11): Show | 17 | HG00673.hp1 HG02083.hp1 HG03098.hp1 others(14): Show |
intron_variant | MODIFIER | c.1057-564_1057-561d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | ||||||
chr4:76125316
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0004g0106 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1057-570_1057-561d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | ||||||
chr4:76125330
|
A | G | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1057-574T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125330 | ||||||
chr4:76125331
|
C | T | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1057-575G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125331 | ||||||
chr4:76125332
|
A | G | 3 | a0002c0002t0003g0046a0002c0002t0003g0071a0002c0002t0003g0075 | 3 | HG01243.hp2 HG04199.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1057-576T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125332 | ||||||
chr4:76125334
|
A | G | 26 | a0002c0002t0003g0001a0002c0002t0003g0012a0002c0002t0003g0027others(23): Show | 35 | HG00597.hp2 HG01099.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1057-578T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125334 | ||||||
chr4:76125335
|
C | T | 3 | a0002c0002t0003g0050a0002c0002t0003g0060a0002c0002t0003g0077 | 3 | NA18977.hp2 NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1057-579G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125335 | ||||||
chr4:76125336
|
A | G | 51 | a0002c0002t0003g0001a0002c0002t0003g0006a0002c0002t0003g0007others(48): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1057-580T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125336 | ||||||
chr4:76125338
|
A | ACGTG | 5 | a0002c0002t0003g0005a0002c0002t0003g0041a0002c0002t0003g0065others(2): Show | 7 | HG00558.hp2 HG00673.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-583_1057-582i others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125338 | ||||||
chr4:76125338
|
A | G | 51 | a0002c0002t0003g0001a0002c0002t0003g0006a0002c0002t0003g0007others(48): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1057-582T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125338 | ||||||
chr4:76125340
|
A | ACGCGCGC | 2 | a0002c0002t0003g0002a0005c0007t0003g0066 | 6 | HG04184.hp1 NA18939.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-585_1057-584i others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125340 | ||||||
chr4:76125340
|
A | G | 58 | a0002c0002t0003g0001a0002c0002t0003g0005a0002c0002t0003g0006others(55): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-584T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125340 | ||||||
chr4:76125342
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-586T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125342 | ||||||
chr4:76125343
|
C | T | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1057-587G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125343 | ||||||
chr4:76125344
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-588T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125344 | ||||||
chr4:76125345
|
C | CGCGCGCT | 3 | a0002c0002t0003g0049a0002c0002t0003g0057a0002c0002t0003g0063 | 3 | HG02040.hp2 NA19084.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1057-590_1057-589i others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125345 | ||||||
chr4:76125346
|
A | G | 64 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(61): Show | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-590T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125346 | ||||||
chr4:76125348
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-592T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125348 | ||||||
chr4:76125350
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-594T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125350 | ||||||
chr4:76125359
|
C | A | 72 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(69): Show | 77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1057-603G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125359 | ||||||
chr4:76125619
|
G | GGAGAGGG others(1): Show |
55 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(52): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1057-871_1057-864d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
G | GGAGGGGG others(1): Show |
21 | a0001c0001t0004g0095a0001c0001t0004g0097a0001c0001t0004g0098others(18): Show | 21 | HG01106.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1057-864_1057-863i others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
G | GGAGGGGG others(9): Show |
32 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0020others(29): Show | 36 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1057-864_1057-863i others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
G | GGAGGGGG others(17): Show |
6 | a0001c0001t0004g0015a0001c0001t0004g0123a0001c0001t0004g0127others(3): Show | 7 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-864_1057-863i others(26): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
G | GGAGGGGG others(25): Show |
1 | a0001c0001t0004g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1057-864_1057-863i others(34): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
G | GGAGGGGG others(10): Show |
1 | a0001c0001t0004g0143 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1057-864_1057-863i others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
G | GGAGGGGG others(9): Show |
1 | a0001c0001t0004g0145 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1057-864_1057-863i others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125619
|
GGAGAGGG others(1): Show |
G | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-871_1057-864d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | ||||||
chr4:76125623
|
A | AGGGAGAG others(1): Show |
8 | a0001c0001t0002g0151a0001c0001t0002g0157a0001c0001t0002g0158others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1057-875_1057-868d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125623 | ||||||
chr4:76125623
|
A | AGGGAGAG others(9): Show |
2 | a0001c0001t0002g0161a0001c0001t0002g0164 | 2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1057-883_1057-868d others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125623 | ||||||
chr4:76125623
|
A | G | 66 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(63): Show | 71 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1057-867T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125623 | ||||||
chr4:76125630
|
GGGGGAGA others(8): Show |
G | 1 | a0001c0001t0002g0191 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1057-889_1057-875d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125630 | ||||||
chr4:76125631
|
G | A | 12 | a0001c0008t0005g0304a0002c0002t0003g0024a0002c0002t0003g0025others(9): Show | 12 | HG02055.hp2 HG02818.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1057-875C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125631 | ||||||
chr4:76125637
|
A | AGGGGGAG others(10): Show |
1 | a0001c0001t0004g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1057-898_1057-882d others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125637 | ||||||
chr4:76125642
|
GAGAGGGG others(8): Show |
G | 5 | a0001c0001t0002g0208a0002c0002t0003g0033a0002c0002t0003g0048others(2): Show | 5 | HG02647.hp2 HG03831.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-901_1057-887d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125642 | ||||||
chr4:76125643
|
AGAGGGG | A | 54 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(51): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-893_1057-888d others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125643 | ||||||
chr4:76125646
|
GGGGGAGA others(8): Show |
G | 1 | a0001c0001t0002g0221 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1057-905_1057-891d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125646 | ||||||
chr4:76125649
|
GGAGAGGG others(1): Show |
G | 5 | a0001c0001t0002g0016a0001c0001t0002g0152a0001c0001t0002g0153others(2): Show | 6 | HG01884.hp2 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-901_1057-894d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125649 | ||||||
chr4:76125655
|
G | A | 7 | a0002c0002t0003g0024a0002c0002t0003g0025a0002c0002t0003g0030others(4): Show | 7 | HG02055.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-899C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125655 | ||||||
chr4:76125655
|
GGAGAGAG others(9): Show |
G | 54 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0017others(51): Show | 62 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1057-915_1057-900d others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125655 | ||||||
chr4:76125655
|
GGAGAGAG others(17): Show |
G | 9 | a0001c0001t0002g0154a0001c0001t0002g0166a0001c0001t0002g0167others(6): Show | 9 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1057-923_1057-900d others(26): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125655 | ||||||
chr4:76125656
|
GAGAGAGG others(8): Show |
G | 1 | a0001c0001t0002g0214 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1057-915_1057-901d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125656 | ||||||
chr4:76125657
|
A | G | 102 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(99): Show | 107 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1057-901T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125657 | ||||||
chr4:76125661
|
A | AGGGGGAG others(10): Show |
1 | a0001c0001t0004g0108 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1057-906_1057-905i others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125661 | ||||||
chr4:76125663
|
G | A | 8 | a0002c0002t0003g0024a0002c0002t0003g0025a0002c0002t0003g0030others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1057-907C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125663 | ||||||
chr4:76125665
|
G | A | 54 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(51): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-909C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125665 | ||||||
chr4:76125667
|
A | T | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-911T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125667 | ||||||
chr4:76125667
|
AGAGAGGG others(2): Show |
A | 54 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(51): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-920_1057-912d others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125667 | ||||||
chr4:76125669
|
AGAGGGAG | A | 7 | a0002c0002t0003g0024a0002c0002t0003g0025a0002c0002t0003g0030others(4): Show | 7 | HG02055.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-920_1057-914d others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125669 | ||||||
chr4:76125671
|
A | G | 27 | a0001c0001t0002g0016a0001c0001t0002g0146a0001c0001t0002g0147others(24): Show | 28 | HG00423.hp2 HG01109.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.1057-915T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125671 | ||||||
chr4:76125673
|
G | GGGGGAGA others(40): Show |
1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-918_1057-917i others(49): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125673 | ||||||
chr4:76125677
|
A | G | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-921T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125677 | ||||||
chr4:76125678
|
GAGGGAGA others(8): Show |
G | 1 | a0001c0001t0002g0216 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1057-937_1057-923d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125678 | ||||||
chr4:76125679
|
A | G | 63 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(60): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1057-923T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125679 | ||||||
chr4:76125681
|
G | GGAGAGGG others(11): Show |
1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-926_1057-925i others(20): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125681 | ||||||
chr4:76125682
|
G | GAGA | 4 | a0002c0002t0003g0033a0002c0002t0003g0048a0002c0002t0003g0068others(1): Show | 4 | HG03831.hp2 HG03927.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-929_1057-927d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125682 | ||||||
chr4:76125685
|
AGGGAG | A | 62 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(59): Show | 83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1057-934_1057-930d others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125685 | ||||||
chr4:76125689
|
A | G | 69 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(66): Show | 78 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1057-933T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125689 | ||||||
chr4:76125690
|
G | GA | 4 | a0002c0002t0003g0033a0002c0002t0003g0048a0002c0002t0003g0068others(1): Show | 4 | HG03831.hp2 HG03927.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-935dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125690 | ||||||
chr4:76125693
|
AGGGAGAA others(3): Show |
A | 1 | a0001c0001t0002g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1057-947_1057-938d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125693 | ||||||
chr4:76125723
|
G | GAGAAGAG others(5): Show |
1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-968_1057-967i others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125723 | ||||||
chr4:76125735
|
A | T | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-979T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125735 | ||||||
chr4:76125737
|
AAGAGGGA others(9): Show |
A | 14 | a0001c0004t0001g0004a0001c0004t0001g0314a0001c0004t0001g0315others(11): Show | 17 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.1057-997_1057-982d others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125737 | ||||||
chr4:76125744
|
A | AGAGAGGG others(9): Show |
1 | a0001c0001t0001g0261 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1057-1004_1057-989 others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125744 | ||||||
chr4:76125744
|
A | C | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-988T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125744 | ||||||
chr4:76125744
|
AGAGAGGG others(1): Show |
A | 45 | a0001c0001t0001g0260a0001c0001t0002g0163a0001c0001t0002g0181others(42): Show | 45 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1057-996_1057-989d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125744 | ||||||
chr4:76125752
|
G | GGAGAGAG others(37): Show |
1 | a0003c0003t0001g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1057-997_1057-996i others(46): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125752
|
G | GGAGAGGG others(11): Show |
59 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(56): Show | 64 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1057-997_1057-996i others(20): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125752
|
G | GGAGAGGG others(74): Show |
2 | a0001c0004t0004g0305a0001c0004t0004g0309 | 2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1057-997_1057-996i others(83): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125752
|
G | GGAGAGGG others(75): Show |
1 | a0001c0004t0004g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1057-997_1057-996i others(84): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125752
|
G | GGAGAGGG others(37): Show |
1 | a0001c0001t0004g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1057-997_1057-996i others(46): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125752
|
G | GGGAGAGG others(4): Show |
2 | a0001c0001t0002g0190a0001c0001t0002g0216 | 2 | HG01978.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1057-997_1057-996i others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125752
|
G | GGGAGAGG others(13): Show |
1 | a0001c0001t0004g0227 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1057-997_1057-996i others(22): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | ||||||
chr4:76125756
|
A | AGGGGGAG others(13): Show |
1 | a0001c0001t0004g0094 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1057-1001_1057-100 others(24): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125756 | ||||||
chr4:76125758
|
G | A | 67 | a0001c0001t0004g0137a0002c0002t0003g0001a0002c0002t0003g0002others(64): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1057-1002C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125758 | ||||||
chr4:76125760
|
G | A | 3 | a0001c0001t0002g0190a0001c0001t0002g0216a0003c0003t0001g0238 | 3 | HG01978.hp2 HG02622.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1057-1004C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125760 | ||||||
chr4:76125760
|
G | GGAGAGAG others(3): Show |
88 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(85): Show | 97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1057-1005_1057-100 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125760 | ||||||
chr4:76125760
|
G | GGGAGAGA others(4): Show |
1 | a0001c0001t0002g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1057-1005_1057-100 others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125760 | ||||||
chr4:76125762
|
A | G | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1006T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125762 | ||||||
chr4:76125764
|
A | AGAGGGAG others(12): Show |
1 | a0001c0001t0004g0128 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1057-1009_1057-100 others(23): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125764 | ||||||
chr4:76125764
|
A | AGAGGGAG others(75): Show |
1 | a0001c0004t0004g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1057-1009_1057-100 others(86): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125764 | ||||||
chr4:76125766
|
G | A | 71 | a0001c0001t0002g0181a0001c0001t0004g0102a0001c0001t0004g0112others(68): Show | 92 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1057-1010C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125766 | ||||||
chr4:76125768
|
GGA | G | 62 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(59): Show | 83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1057-1014_1057-101 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125768 | ||||||
chr4:76125770
|
A | G | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1014T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125770 | ||||||
chr4:76125774
|
A | G | 4 | a0002c0002t0003g0044a0002c0002t0003g0055a0002c0002t0003g0056others(1): Show | 4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1018T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125774 | ||||||
chr4:76125774
|
AGGGAGAG others(3): Show |
A | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-1028_1057-101 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125774 | ||||||
chr4:76125776
|
G | A | 4 | a0002c0002t0003g0044a0002c0002t0003g0055a0002c0002t0003g0056others(1): Show | 4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1020C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125776 | ||||||
chr4:76125778
|
A | G | 4 | a0001c0001t0002g0181a0001c0001t0004g0102a0001c0001t0004g0112others(1): Show | 4 | HG01981.hp1 HG03540.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-1022T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125778 | ||||||
chr4:76125784
|
G | A | 63 | a0001c0001t0002g0181a0002c0002t0003g0001a0002c0002t0003g0002others(60): Show | 84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1057-1028C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | ||||||
chr4:76125784
|
G | GGGGAGAG others(1): Show |
92 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(89): Show | 101 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1057-1036_1057-102 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | ||||||
chr4:76125784
|
G | GGGGAGAG others(9): Show |
1 | a0001c0001t0002g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1057-1029_1057-102 others(20): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | ||||||
chr4:76125784
|
G | GGGGGAGA others(26): Show |
1 | a0001c0001t0004g0136 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1057-1029_1057-102 others(37): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | ||||||
chr4:76125786
|
G | A | 4 | a0002c0002t0003g0044a0002c0002t0003g0055a0002c0002t0003g0056others(1): Show | 4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1030C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125786 | ||||||
chr4:76125788
|
AG | A | 4 | a0002c0002t0003g0044a0002c0002t0003g0055a0002c0002t0003g0056others(1): Show | 4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1033delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125788 | ||||||
chr4:76125789
|
G | GAGAGGGA others(13): Show |
1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1034_1057-103 others(24): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125789 | ||||||
chr4:76125790
|
AGAGGG | A | 62 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(59): Show | 83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1057-1039_1057-103 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125790 | ||||||
chr4:76125791
|
G | GAGGGAGA others(19): Show |
2 | a0001c0001t0004g0102a0001c0001t0004g0112 | 2 | HG01981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1057-1036_1057-103 others(30): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125791 | ||||||
chr4:76125791
|
G | GAGGGAGA others(1): Show |
63 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(60): Show | 68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1057-1036_1057-103 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125791 | ||||||
chr4:76125791
|
G | T | 1 | a0001c0001t0004g0136 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1057-1035C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125791 | ||||||
chr4:76125792
|
AGGGAGAG others(28): Show |
A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207 | 3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1071_1057-103 others(39): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125792 | ||||||
chr4:76125797
|
G | GAA | 3 | a0002c0002t0003g0044a0002c0002t0003g0055a0002c0002t0003g0056 | 3 | NA18968.hp1 NA18989.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1057-1042_1057-104 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125797 | ||||||
chr4:76125802
|
A | G | 3 | a0002c0002t0003g0044a0002c0002t0003g0055a0002c0002t0003g0056 | 3 | NA18968.hp1 NA18989.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1057-1046T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125802 | ||||||
chr4:76125805
|
G | A | 63 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(60): Show | 84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1057-1049C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125805 | ||||||
chr4:76125807
|
G | T | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1051C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125807 | ||||||
chr4:76125808
|
A | G | 63 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(60): Show | 84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1057-1052T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125808 | ||||||
chr4:76125813
|
GA | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1058delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125813 | ||||||
chr4:76125822
|
GAA | G | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1057-1068_1057-106 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125822 | ||||||
chr4:76125824
|
A | G | 1 | a0002c0002t0003g0070 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1057-1068T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125824 | ||||||
chr4:76125827
|
G | A | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1057-1071C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125827 | ||||||
chr4:76125827
|
G | GGGGAGAG others(18): Show |
1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1072_1057-107 others(29): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125827 | ||||||
chr4:76125827
|
GGGGAGAG others(1): Show |
G | 14 | a0001c0004t0001g0004a0001c0004t0001g0314a0001c0004t0001g0315others(11): Show | 17 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.1057-1079_1057-107 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125827 | ||||||
chr4:76125828
|
G | T | 1 | a0001c0001t0004g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1072C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125828 | ||||||
chr4:76125829
|
G | A | 1 | a0002c0002t0003g0070 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1057-1073C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125829 | ||||||
chr4:76125837
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1081C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125837 | ||||||
chr4:76125847
|
A | G | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207 | 3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1091T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125847 | ||||||
chr4:76125851
|
A | G | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207 | 3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1095T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125851 | ||||||
chr4:76125855
|
G | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207 | 3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1099C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125855 | ||||||
chr4:76125857
|
A | G | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207 | 3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1101T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125857 | ||||||
chr4:76125859
|
G | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207 | 3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1103C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125859 | ||||||
chr4:76125859
|
G | GGA | 64 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(61): Show | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-1104_1057-110 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125859 | ||||||
chr4:76125861
|
G | A | 67 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207others(64): Show | 88 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1057-1105C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125861 | ||||||
chr4:76125865
|
G | A | 68 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0207others(65): Show | 89 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1057-1109C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | ||||||
chr4:76125865
|
G | GGAGAGA | 69 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(66): Show | 74 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1057-1115_1057-111 others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | ||||||
chr4:76125865
|
G | GGAGAGAG others(1): Show |
92 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(89): Show | 101 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1057-1117_1057-111 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | ||||||
chr4:76125865
|
G | GGAGAGAG others(3): Show |
1 | a0001c0001t0002g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1057-1119_1057-111 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | ||||||
chr4:76125922
|
C | G | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1166G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125922 | ||||||
chr4:76125936
|
ATAAT | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1184_1057-118 others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125936 | ||||||
chr4:76125964
|
A | T | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1208T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125964 | ||||||
chr4:76125965
|
T | G | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1209A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125965 | ||||||
chr4:76125968
|
A | T | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1212T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125968 | ||||||
chr4:76125974
|
C | G | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1218G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125974 | ||||||
chr4:76125975
|
A | T | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1219T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125975 | ||||||
chr4:76125977
|
C | A | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1221G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125977 | ||||||
chr4:76125982
|
T | A | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1226A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125982 | ||||||
chr4:76125984
|
T | G | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1228A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125984 | ||||||
chr4:76125985
|
G | T | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1229C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125985 | ||||||
chr4:76125989
|
G | T | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1233C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125989 | ||||||
chr4:76125991
|
A | AAAAAGGT others(6): Show |
1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1236_1057-123 others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125991 | ||||||
chr4:76125998
|
T | G | 1 | a0001c0001t0004g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1242A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125998 | ||||||
chr4:76126066
|
G | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1057-1310C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126066 | ||||||
chr4:76126115
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1359C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126115 | ||||||
chr4:76126351
|
T | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1595A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126351 | ||||||
chr4:76126425
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1669G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126425 | ||||||
chr4:76126468
|
G | C | 1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1057-1712C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126468 | ||||||
chr4:76126634
|
ACCATCTA others(18): Show |
A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1903_1057-187 others(29): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126634 | ||||||
chr4:76126692
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1936C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126692 | ||||||
chr4:76126743
|
G | A | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1057-1987C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126743 | ||||||
chr4:76126761
|
T | C | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1057-2005A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126761 | ||||||
chr4:76126934
|
G | A | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-2178C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126934 | ||||||
chr4:76127046
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1057-2290T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127046 | ||||||
chr4:76127154
|
T | C | 250 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(247): Show | 288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1057-2398A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127154 | ||||||
chr4:76127171
|
G | A | 1 | a0003c0003t0001g0270 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1057-2415C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127171 | ||||||
chr4:76127204
|
G | A | 64 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(61): Show | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-2448C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127204 | ||||||
chr4:76127348
|
C | T | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-2592G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127348 | ||||||
chr4:76127381
|
G | A | 1 | a0001c0004t0001g0325 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1057-2625C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127381 | ||||||
chr4:76127385
|
T | C | 67 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(64): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1057-2629A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127385 | ||||||
chr4:76127389
|
G | A | 64 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(61): Show | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-2633C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127389 | ||||||
chr4:76127411
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-2655C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127411 | ||||||
chr4:76127415
|
G | A | 1 | a0001c0001t0004g0093 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1057-2659C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127415 | ||||||
chr4:76127432
|
C | CA | 12 | a0001c0001t0001g0245a0001c0001t0001g0250a0001c0001t0001g0254others(9): Show | 12 | HG00597.hp1 HG01109.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1057-2677dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127432
|
C | CAAA | 52 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(49): Show | 73 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1057-2679_1057-267 others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127432
|
C | CAAAA | 10 | a0002c0002t0003g0026a0002c0002t0003g0033a0002c0002t0003g0045others(7): Show | 10 | HG00609.hp1 HG01243.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1057-2680_1057-267 others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127432
|
C | CAAAAA | 6 | a0001c0001t0002g0160a0001c0001t0002g0183a0001c0001t0002g0189others(3): Show | 6 | HG02976.hp2 NA18946.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-2681_1057-267 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127432
|
C | CAAAAAA | 59 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0017others(56): Show | 67 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1057-2682_1057-267 others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127432
|
C | CAAAAAAA | 26 | a0001c0001t0002g0016a0001c0001t0002g0146a0001c0001t0002g0147others(23): Show | 27 | HG00423.hp2 HG01258.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1057-2683_1057-267 others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127432
|
CA | C | 13 | a0001c0001t0001g0256a0001c0001t0004g0098a0001c0001t0004g0103others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1057-2677delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | ||||||
chr4:76127532
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-2776G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127532 | ||||||
chr4:76127545
|
C | T | 250 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(247): Show | 288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1057-2789G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127545 | ||||||
chr4:76127706
|
G | A | 2 | a0003c0003t0001g0289a0003c0003t0001g0293 | 2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1056+2950C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127706 | ||||||
chr4:76127750
|
G | A | 1 | a0001c0001t0005g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1056+2906C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127750 | ||||||
chr4:76127824
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+2832T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127824 | ||||||
chr4:76127859
|
G | A | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1056+2797C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127859 | ||||||
chr4:76127862
|
C | T | 4 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(1): Show | 4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+2794G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127862 | ||||||
chr4:76128112
|
T | C | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1056+2544A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128112 | ||||||
chr4:76128117
|
A | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+2539T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128117 | ||||||
chr4:76128134
|
A | G | 4 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(1): Show | 4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+2522T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128134 | ||||||
chr4:76128367
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+2289G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128367 | ||||||
chr4:76128396
|
G | GA | 10 | a0001c0001t0001g0245a0001c0001t0002g0146a0001c0001t0002g0147others(7): Show | 10 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1056+2259dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128396 | ||||||
chr4:76128396
|
G | GAA | 158 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(155): Show | 172 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1056+2258_1056+225 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128396 | ||||||
chr4:76128531
|
G | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1056+2125C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128531 | ||||||
chr4:76128650
|
T | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+2006A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128650 | ||||||
chr4:76128947
|
G | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1056+1709C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128947 | ||||||
chr4:76128985
|
C | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1671G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128985 | ||||||
chr4:76129024
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1632A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129024 | ||||||
chr4:76129071
|
G | T | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1056+1585C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129071 | ||||||
chr4:76129088
|
A | G | 1 | a0001c0001t0004g0125 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1056+1568T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129088 | ||||||
chr4:76129140
|
T | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1056+1516A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129140 | ||||||
chr4:76129155
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1501T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129155 | ||||||
chr4:76129208
|
C | T | 4 | a0003c0003t0001g0272a0003c0003t0001g0277a0003c0003t0001g0279others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056+1448G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129208 | ||||||
chr4:76129209
|
G | C | 2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1056+1447C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129209 | ||||||
chr4:76129221
|
TAAAAG | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1430_1056+143 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129221 | ||||||
chr4:76129470
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1186C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129470 | ||||||
chr4:76129518
|
A | C | 1 | a0002c0002t0003g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1056+1138T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129518 | ||||||
chr4:76129614
|
T | C | 1 | a0003c0003t0001g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1056+1042A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129614 | ||||||
chr4:76129781
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1056+875G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129781 | ||||||
chr4:76129820
|
G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0246others(1): Show | 4 | HG01081.hp2 HG01243.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+836C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129820 | ||||||
chr4:76129843
|
C | T | 3 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148 | 3 | HG01891.hp2 HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1056+813G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129843 | ||||||
chr4:76129863
|
C | CA | 39 | a0001c0001t0001g0023a0001c0001t0001g0232a0001c0001t0001g0234others(36): Show | 41 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1056+792dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | ||||||
chr4:76129863
|
CA | C | 24 | a0001c0001t0002g0175a0001c0001t0002g0180a0001c0001t0002g0184others(21): Show | 24 | HG01358.hp1 HG01891.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.1056+792delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | ||||||
chr4:76129863
|
CAA | C | 45 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0017others(42): Show | 53 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1056+791_1056+792d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | ||||||
chr4:76129863
|
CAAA | C | 30 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0157others(27): Show | 30 | HG01069.hp2 HG01109.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.1056+790_1056+792d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | ||||||
chr4:76129863
|
CAAAA | C | 64 | a0001c0001t0002g0016a0001c0001t0002g0146a0001c0001t0002g0149others(61): Show | 68 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.1056+789_1056+792d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | ||||||
chr4:76129882
|
A | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01081.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1056+774T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129882 | ||||||
chr4:76129883
|
AAAAAACC others(5): Show |
A | 54 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(51): Show | 74 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1056+761_1056+772d others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129883 | ||||||
chr4:76129884
|
AAAAACCT others(4): Show |
A | 10 | a0002c0002t0003g0013a0002c0002t0003g0036a0002c0002t0003g0057others(7): Show | 11 | HG01346.hp2 HG02015.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1056+761_1056+771d others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129884 | ||||||
chr4:76129885
|
AAAACCTT others(3): Show |
A | 2 | a0002c0002t0003g0024a0002c0002t0003g0025 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1056+761_1056+770d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129885 | ||||||
chr4:76129966
|
G | GT | 15 | a0001c0001t0001g0232a0001c0001t0001g0247a0001c0001t0001g0248others(12): Show | 15 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1056+689dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
G | GTT | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0233others(8): Show | 13 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1056+688_1056+689d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GT | G | 23 | a0003c0003t0001g0237a0003c0003t0001g0238a0003c0003t0001g0239others(20): Show | 23 | HG00140.hp1 HG00738.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1056+689delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTT | G | 13 | a0003c0003t0001g0231a0003c0003t0001g0241a0003c0003t0001g0242others(10): Show | 13 | HG01069.hp2 HG01168.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1056+688_1056+689d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTT | G | 7 | a0001c0004t0001g0314a0001c0004t0001g0315a0001c0004t0001g0316others(4): Show | 7 | HG02976.hp1 NA18906.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.1056+687_1056+689d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTT | G | 7 | a0001c0001t0002g0082a0001c0001t0002g0178a0001c0004t0001g0004others(4): Show | 10 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+686_1056+689d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTT | G | 34 | a0001c0001t0002g0003a0001c0001t0002g0018a0001c0001t0002g0083others(31): Show | 38 | HG00544.hp2 HG01070.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1056+685_1056+689d others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTT | G | 28 | a0001c0001t0002g0009a0001c0001t0002g0017a0001c0001t0002g0019others(25): Show | 32 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1056+684_1056+689d others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(1): Show |
G | 14 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1056+682_1056+689d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(2): Show |
G | 20 | a0001c0001t0002g0016a0001c0001t0002g0149a0001c0001t0002g0150others(17): Show | 21 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.1056+681_1056+689d others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(3): Show |
G | 20 | a0001c0001t0004g0115a0001c0004t0004g0306a0001c0004t0004g0309others(17): Show | 21 | HG00597.hp2 HG01243.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1056+680_1056+689d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(4): Show |
G | 71 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0097others(68): Show | 91 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1056+679_1056+689d others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(5): Show |
G | 44 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(41): Show | 49 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1056+678_1056+689d others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0004t0004g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1056+677_1056+689d others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129966
|
GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0005g0085 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1056+669_1056+689d others(23): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | ||||||
chr4:76129980
|
T | G | 3 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110 | 3 | HG03239.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1056+676A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129980 | ||||||
chr4:76130011
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+645G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130011 | ||||||
chr4:76130036
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+620T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130036 | ||||||
chr4:76130040
|
G | T | 1 | a0001c0001t0004g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1056+616C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130040 | ||||||
chr4:76130044
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1056+612C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130044 | ||||||
chr4:76130115
|
G | A | 1 | a0001c0004t0004g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1056+541C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130115 | ||||||
chr4:76130183
|
A | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+473T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130183 | ||||||
chr4:76130496
|
T | A | 34 | a0001c0001t0002g0016a0001c0001t0002g0146a0001c0001t0002g0147others(31): Show | 35 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1056+160A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130496 | ||||||
chr4:76130509
|
G | T | 32 | a0001c0001t0002g0016a0001c0001t0002g0146a0001c0001t0002g0147others(29): Show | 33 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1056+147C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130509 | ||||||
chr4:76130550
|
G | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+106C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130550 | ||||||
chr4:76130825
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.963-76G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76130825 | ||||||
chr4:76130878
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.963-129T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76130878 | ||||||
chr4:76130915
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.963-166T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76130915 | ||||||
chr4:76131031
|
C | A | 1 | a0002c0002t0003g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.962+199G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76131031 | ||||||
chr4:76131038
|
C | CT | 64 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(61): Show | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.962+191dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76131038 | ||||||
chr4:76131135
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.962+95A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76131135 | ||||||
chr4:76131377
|
T | C | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.908-93A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131377 | ||||||
chr4:76131499
|
T | C | 1 | a0002c0002t0003g0075 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908-215A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131499 | ||||||
chr4:76131567
|
T | C | 1 | a0002c0002t0003g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.908-283A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131567 | ||||||
chr4:76131675
|
GA | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.908-392delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131675 | ||||||
chr4:76131696
|
T | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(69): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.908-412A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131696 | ||||||
chr4:76131971
|
T | C | 3 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086 | 3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.907+552A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131971 | ||||||
chr4:76131975
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.907+548C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131975 | ||||||
chr4:76132036
|
T | C | 1 | a0001c0001t0004g0142 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.907+487A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132036 | ||||||
chr4:76132049
|
A | G | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.907+474T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132049 | ||||||
chr4:76132118
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.907+405C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132118 | ||||||
chr4:76132335
|
C | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.907+188G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132335 | ||||||
chr4:76132380
|
A | T | 1 | a0003c0003t0001g0290 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907+143T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132380 | ||||||
chr4:76132405
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.907+118T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132405 | ||||||
chr4:76132409
|
C | T | 289 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(286): Show | 327 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.907+114G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132409 | ||||||
chr4:76132489
|
T | C | 1 | a0002c0002t0003g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.907+34A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132489 | ||||||
chr4:76132746
|
A | G | 1 | a0001c0004t0004g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.711-27T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132746 | ||||||
chr4:76132826
|
A | T | 1 | a0001c0001t0002g0185 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.711-107T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132826 | ||||||
chr4:76132829
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.711-110A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132829 | ||||||
chr4:76132860
|
C | CT | 9 | a0001c0001t0002g0170a0001c0001t0004g0095a0001c0001t0004g0097others(6): Show | 9 | HG00438.hp1 HG00597.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.711-142dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132860 | ||||||
chr4:76132860
|
CT | C | 9 | a0001c0001t0002g0016a0001c0001t0002g0152a0001c0001t0002g0153others(6): Show | 10 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.711-142delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132860 | ||||||
chr4:76132879
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-160G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132879 | ||||||
chr4:76132991
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-272G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132991 | ||||||
chr4:76133001
|
G | A | 58 | a0001c0004t0001g0004a0001c0004t0001g0314a0001c0004t0001g0315others(55): Show | 61 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.711-282C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133001 | ||||||
chr4:76133016
|
CAT | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-299_711-298del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133016 | ||||||
chr4:76133021
|
A | G | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.711-302T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133021 | ||||||
chr4:76133029
|
C | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-310G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133029 | ||||||
chr4:76133047
|
GAT | G | 157 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(154): Show | 187 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.711-330_711-329del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133047 | ||||||
chr4:76133051
|
T | G | 64 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(61): Show | 85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.711-332A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133051 | ||||||
chr4:76133057
|
T | C | 64 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(61): Show | 69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.711-338A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133057 | ||||||
chr4:76133062
|
A | T | 1 | a0001c0001t0002g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.711-343T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133062 | ||||||
chr4:76133063
|
T | C | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711-344A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133063 | ||||||
chr4:76133064
|
A | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.711-345T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133064 | ||||||
chr4:76133144
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-425G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133144 | ||||||
chr4:76133146
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-427G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133146 | ||||||
chr4:76133152
|
C | T | 4 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(1): Show | 4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-433G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133152 | ||||||
chr4:76133272
|
T | C | 2 | a0001c0004t0004g0305a0001c0004t0004g0306 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.711-553A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133272 | ||||||
chr4:76133312
|
G | GT | 95 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(92): Show | 104 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.711-594dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133312 | ||||||
chr4:76133312
|
GT | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-594delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133312 | ||||||
chr4:76133367
|
T | G | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.711-648A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133367 | ||||||
chr4:76133398
|
T | C | 70 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(67): Show | 91 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.711-679A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133398 | ||||||
chr4:76133462
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+713G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133462 | ||||||
chr4:76133469
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+706G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133469 | ||||||
chr4:76133553
|
C | T | 67 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(64): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.710+622G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133553 | ||||||
chr4:76133697
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+478G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133697 | ||||||
chr4:76133706
|
T | C | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+469A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133706 | ||||||
chr4:76133732
|
G | GA | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+442_710+443ins others(1): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133732 | ||||||
chr4:76133741
|
T | C | 1 | a0001c0004t0001g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.710+434A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133741 | ||||||
chr4:76133911
|
A | G | 1 | a0001c0001t0004g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.710+264T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133911 | ||||||
chr4:76133917
|
A | G | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.710+258T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133917 | ||||||
chr4:76134038
|
C | G | 1 | a0002c0002t0003g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.710+137G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76134038 | ||||||
chr4:76134425
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.523-63T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134425 | ||||||
chr4:76134473
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0170a0001c0001t0002g0171 | 3 | HG02572.hp2 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.523-111C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134473 | ||||||
chr4:76134511
|
C | T | 3 | a0002c0002t0003g0032a0002c0002t0003g0039a0002c0002t0003g0040 | 3 | HG01099.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.523-149G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134511 | ||||||
chr4:76134593
|
CTT | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.523-233_523-232del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134593 | ||||||
chr4:76134734
|
A | ATTG | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.523-373_523-372ins others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134734 | ||||||
chr4:76134760
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.523-398A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134760 | ||||||
chr4:76134770
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.523-408C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134770 | ||||||
chr4:76134909
|
T | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.523-547A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134909 | ||||||
chr4:76135020
|
A | C | 64 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(61): Show | 69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.523-658T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135020 | ||||||
chr4:76135028
|
CATA | C | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181 | 3 | HG01891.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.523-669_523-667del others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135028 | ||||||
chr4:76135139
|
G | T | 12 | a0003c0003t0001g0236a0003c0003t0001g0270a0003c0003t0001g0272others(9): Show | 12 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-777C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135139 | ||||||
chr4:76135306
|
A | C | 1 | a0001c0001t0002g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.522+880T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135306 | ||||||
chr4:76135311
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+875G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135311 | ||||||
chr4:76135345
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+841C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135345 | ||||||
chr4:76135373
|
A | G | 2 | a0001c0001t0005g0090a0001c0001t0005g0091 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.522+813T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135373 | ||||||
chr4:76135578
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+608T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135578 | ||||||
chr4:76135585
|
T | C | 1 | a0003c0003t0001g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.522+601A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135585 | ||||||
chr4:76135596
|
A | T | 1 | a0001c0001t0004g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.522+590T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135596 | ||||||
chr4:76135655
|
G | A | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.522+531C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135655 | ||||||
chr4:76135734
|
A | G | 2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.522+452T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135734 | ||||||
chr4:76135751
|
G | A | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.522+435C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135751 | ||||||
chr4:76135828
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+358A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135828 | ||||||
chr4:76135870
|
T | C | 1 | a0001c0001t0004g0143 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.522+316A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135870 | ||||||
chr4:76136595
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-183G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136595 | ||||||
chr4:76136669
|
C | A | 289 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(286): Show | 327 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.296-257G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136669 | ||||||
chr4:76136731
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-319C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136731 | ||||||
chr4:76136752
|
G | T | 58 | a0001c0004t0001g0004a0001c0004t0001g0314a0001c0004t0001g0315others(55): Show | 61 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.296-340C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136752 | ||||||
chr4:76136783
|
G | A | 1 | a0003c0003t0001g0296 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.296-371C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136783 | ||||||
chr4:76136904
|
T | G | 2 | a0002c0002t0003g0076a0002c0002t0003g0077 | 2 | HG02129.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.296-492A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136904 | ||||||
chr4:76136981
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-569T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136981 | ||||||
chr4:76136988
|
TTTTCTAA others(40): Show |
T | 1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-623_296-577del others(47): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136988 | ||||||
chr4:76137096
|
A | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-684T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137096 | ||||||
chr4:76137098
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-686G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137098 | ||||||
chr4:76137165
|
A | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-753T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137165 | ||||||
chr4:76137258
|
A | G | 7 | a0001c0001t0002g0016a0001c0001t0002g0152a0001c0001t0002g0153others(4): Show | 8 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-846T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137258 | ||||||
chr4:76137365
|
C | T | 67 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(64): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.296-953G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137365 | ||||||
chr4:76137617
|
G | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1205C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137617 | ||||||
chr4:76137635
|
G | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1223C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137635 | ||||||
chr4:76137642
|
C | CACTT | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1231_296-1230i others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137642 | ||||||
chr4:76137676
|
AG | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.296-1265delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137676 | ||||||
chr4:76137830
|
T | C | 42 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(39): Show | 46 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.296-1418A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137830 | ||||||
chr4:76137850
|
G | C | 1 | a0003c0003t0001g0297 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.296-1438C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137850 | ||||||
chr4:76137877
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1465A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137877 | ||||||
chr4:76137877
|
TAGC | T | 3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.296-1468_296-1466d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137877 | ||||||
chr4:76137911
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1499A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137911 | ||||||
chr4:76137944
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1532T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137944 | ||||||
chr4:76137966
|
G | C | 2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-1554C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137966 | ||||||
chr4:76137977
|
G | A | 235 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(232): Show | 270 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.296-1565C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137977 | ||||||
chr4:76138022
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.296-1610C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138022 | ||||||
chr4:76138268
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1856G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138268 | ||||||
chr4:76138329
|
TG | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1918delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138329 | ||||||
chr4:76138361
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1949G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138361 | ||||||
chr4:76138654
|
G | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-2242C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138654 | ||||||
chr4:76138696
|
G | GCACTTCA others(39): Show |
1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-2285_296-2284i others(48): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138696 | ||||||
chr4:76138817
|
A | T | 4 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(1): Show | 4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2405T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138817 | ||||||
chr4:76138959
|
AT | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2548delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138959 | ||||||
chr4:76139007
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.296-2595G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139007 | ||||||
chr4:76139260
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2848C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139260 | ||||||
chr4:76139311
|
T | C | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | NA18612.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.296-2899A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139311 | ||||||
chr4:76139322
|
C | T | 67 | a0001c0008t0005g0304a0002c0002t0003g0001a0002c0002t0003g0002others(64): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.296-2910G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139322 | ||||||
chr4:76139350
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-2938T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139350 | ||||||
chr4:76139426
|
T | TA | 59 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0017others(56): Show | 67 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.296-3015dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139426 | ||||||
chr4:76139452
|
C | CAGA | 71 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(68): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.296-3043_296-3041d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139452 | ||||||
chr4:76139493
|
T | C | 2 | a0001c0001t0005g0090a0001c0001t0005g0091 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-3081A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139493 | ||||||
chr4:76139716
|
G | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.296-3304C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139716 | ||||||
chr4:76139750
|
C | T | 67 | a0001c0008t0005g0304a0002c0002t0003g0001a0002c0002t0003g0002others(64): Show | 88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.296-3338G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139750 | ||||||
chr4:76139917
|
T | G | 2 | a0001c0001t0005g0090a0001c0001t0005g0091 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-3505A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139917 | ||||||
chr4:76139972
|
T | C | 1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-3560A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139972 | ||||||
chr4:76139977
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-3565C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139977 | ||||||
chr4:76140113
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-3701C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140113 | ||||||
chr4:76140285
|
G | GT | 70 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(67): Show | 90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.295+3863dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140285 | ||||||
chr4:76140285
|
G | GTT | 7 | a0002c0002t0003g0011a0002c0002t0003g0024a0002c0002t0003g0036others(4): Show | 8 | HG01928.hp2 HG03453.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+3862_295+3863d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140285 | ||||||
chr4:76140285
|
GT | G | 68 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(65): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.295+3863delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140285 | ||||||
chr4:76140363
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+3786C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140363 | ||||||
chr4:76140387
|
G | A | 3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.295+3762C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140387 | ||||||
chr4:76140447
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3702T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140447 | ||||||
chr4:76140682
|
C | T | 2 | a0002c0002t0003g0028a0002c0002t0003g0035 | 2 | HG03834.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.295+3467G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140682 | ||||||
chr4:76140683
|
A | G | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+3466T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140683 | ||||||
chr4:76140687
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3462C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140687 | ||||||
chr4:76140694
|
T | C | 4 | a0003c0005t0001g0310a0003c0005t0001g0311a0003c0005t0001g0312others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+3455A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140694 | ||||||
chr4:76140741
|
G | A | 1 | a0001c0001t0004g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.295+3408C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140741 | ||||||
chr4:76140837
|
G | C | 1 | a0002c0002t0003g0026 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.295+3312C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140837 | ||||||
chr4:76140942
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3207A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140942 | ||||||
chr4:76141015
|
G | A | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.295+3134C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141015 | ||||||
chr4:76141037
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3112T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141037 | ||||||
chr4:76141059
|
C | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3090G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141059 | ||||||
chr4:76141149
|
T | A | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.295+3000A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141149 | ||||||
chr4:76141154
|
A | AATACATG others(1): Show |
93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+2987_295+2994d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141154 | ||||||
chr4:76141247
|
G | A | 1 | a0001c0001t0004g0145 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.295+2902C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141247 | ||||||
chr4:76141251
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2898T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141251 | ||||||
chr4:76141252
|
T | C | 3 | a0001c0004t0004g0305a0001c0004t0004g0306a0001c0004t0004g0309 | 3 | HG02280.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.295+2897A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141252 | ||||||
chr4:76141397
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2752A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141397 | ||||||
chr4:76141509
|
C | T | 1 | a0003c0003t0001g0287 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.295+2640G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141509 | ||||||
chr4:76141656
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.295+2493C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141656 | ||||||
chr4:76141711
|
GT | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2437delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141711 | ||||||
chr4:76141758
|
A | AG | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2390_295+2391i others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141758 | ||||||
chr4:76141810
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2339G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141810 | ||||||
chr4:76141821
|
C | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | NA18612.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.295+2328G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141821 | ||||||
chr4:76141861
|
T | C | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+2288A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141861 | ||||||
chr4:76141887
|
T | TA | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.295+2261dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141887 | ||||||
chr4:76141895
|
C | A | 1 | a0001c0001t0002g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.295+2254G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141895 | ||||||
chr4:76142090
|
C | T | 1 | a0001c0001t0004g0094 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.295+2059G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142090 | ||||||
chr4:76142137
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2012G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142137 | ||||||
chr4:76142162
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.295+1987C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142162 | ||||||
chr4:76142259
|
A | G | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+1890T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142259 | ||||||
chr4:76142275
|
C | T | 1 | a0001c0004t0004g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.295+1874G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142275 | ||||||
chr4:76142344
|
C | T | 3 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0218 | 3 | HG02809.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.295+1805G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142344 | ||||||
chr4:76142388
|
G | A | 250 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(247): Show | 288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.295+1761C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142388 | ||||||
chr4:76142396
|
G | A | 3 | a0003c0003t0001g0265a0003c0003t0001g0266a0003c0003t0001g0286 | 3 | HG01255.hp1 HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.295+1753C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142396 | ||||||
chr4:76142510
|
G | A | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+1639C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142510 | ||||||
chr4:76142513
|
T | A | 6 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1636A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142513 | ||||||
chr4:76142741
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+1408C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142741 | ||||||
chr4:76142867
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+1282A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142867 | ||||||
chr4:76142963
|
C | T | 3 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086 | 3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.295+1186G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142963 | ||||||
chr4:76143017
|
T | C | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+1132A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143017 | ||||||
chr4:76143073
|
T | A | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.295+1076A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143073 | ||||||
chr4:76143118
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+1031C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143118 | ||||||
chr4:76143172
|
C | T | 3 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0068 | 3 | HG02735.hp1 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.295+977G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143172 | ||||||
chr4:76143212
|
A | C | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+937T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143212 | ||||||
chr4:76143332
|
G | A | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+817C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143332 | ||||||
chr4:76143340
|
G | A | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+809C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143340 | ||||||
chr4:76143344
|
A | G | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.295+805T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143344 | ||||||
chr4:76143387
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+762G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143387 | ||||||
chr4:76143406
|
C | A | 3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.295+743G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143406 | ||||||
chr4:76143426
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+723T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143426 | ||||||
chr4:76143433
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+716C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143433 | ||||||
chr4:76143436
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+713A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143436 | ||||||
chr4:76143476
|
C | A | 1 | a0001c0001t0002g0218 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.295+673G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143476 | ||||||
chr4:76143534
|
G | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+615C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143534 | ||||||
chr4:76143553
|
G | A | 3 | a0003c0003t0001g0231a0003c0003t0001g0267a0003c0003t0001g0268 | 3 | HG02258.hp2 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.295+596C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143553 | ||||||
chr4:76143599
|
G | A | 1 | a0002c0002t0003g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.295+550C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143599 | ||||||
chr4:76143690
|
T | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+459A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143690 | ||||||
chr4:76143786
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+363G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143786 | ||||||
chr4:76143989
|
C | T | 93 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(90): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+160G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143989 | ||||||
chr4:76144070
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+79T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76144070 | ||||||
chr4:76144111
|
C | T | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+38G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76144111 | ||||||
chr4:76144135
|
A | C | 1 | a0002c0002t0003g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.295+14T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76144135 | ||||||
chr4:76144323
|
T | TA | 12 | a0003c0003t0001g0287a0003c0003t0001g0288a0003c0003t0001g0289others(9): Show | 12 | HG01255.hp2 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-32dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144323 | ||||||
chr4:76144323
|
TAA | T | 166 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(163): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.152-33_152-32delTT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144323 | ||||||
chr4:76144323
|
TAAA | T | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.152-34_152-32delTT others(1): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144323 | ||||||
chr4:76144365
|
T | C | 228 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(225): Show | 263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.151+25A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144365 | ||||||
chr4:76144978
|
T | G | 1 | a0001c0001t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.68-505A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76144978 | ||||||
chr4:76144993
|
G | C | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-520C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76144993 | ||||||
chr4:76144994
|
A | C | 1 | a0002c0002t0003g0026 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-521T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76144994 | ||||||
chr4:76145084
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-611G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145084 | ||||||
chr4:76145089
|
G | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-616C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145089 | ||||||
chr4:76145090
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-617C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145090 | ||||||
chr4:76145104
|
G | A | 1 | a0002c0002t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.68-631C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145104 | ||||||
chr4:76145119
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-646G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145119 | ||||||
chr4:76145122
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-649A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145122 | ||||||
chr4:76145148
|
G | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-675C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145148 | ||||||
chr4:76145149
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.68-676A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145149 | ||||||
chr4:76145175
|
G | A | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-702C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145175 | ||||||
chr4:76145177
|
G | C | 1 | a0002c0002t0003g0026 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-704C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145177 | ||||||
chr4:76145178
|
C | T | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-705G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145178 | ||||||
chr4:76145183
|
C | T | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.68-710G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145183 | ||||||
chr4:76145190
|
C | T | 2 | a0001c0004t0004g0305a0001c0004t0004g0306 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.68-717G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145190 | ||||||
chr4:76145191
|
G | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-718C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145191 | ||||||
chr4:76145234
|
C | T | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-761G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145234 | ||||||
chr4:76145290
|
C | T | 5 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-817G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145290 | ||||||
chr4:76145292
|
C | T | 250 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(247): Show | 288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.68-819G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145292 | ||||||
chr4:76145317
|
C | CA | 29 | a0001c0001t0001g0285a0001c0001t0005g0087a0001c0001t0005g0091others(26): Show | 29 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-845dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | ||||||
chr4:76145317
|
CA | C | 59 | a0001c0001t0001g0230a0001c0001t0002g0220a0001c0001t0002g0221others(56): Show | 80 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.68-845delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | ||||||
chr4:76145317
|
CAA | C | 63 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0018others(60): Show | 70 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.68-846_68-845delTT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | ||||||
chr4:76145317
|
CAAA | C | 94 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0146others(91): Show | 101 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.68-847_68-845delTT others(1): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | ||||||
chr4:76145317
|
CAAAA | C | 6 | a0001c0001t0004g0093a0001c0004t0004g0302a0001c0004t0004g0305others(3): Show | 6 | HG02280.hp1 HG02818.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-848_68-845delTT others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | ||||||
chr4:76145370
|
C | CT | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-898dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145370 | ||||||
chr4:76145425
|
T | C | 4 | a0002c0002t0003g0078a0002c0002t0003g0079a0002c0002t0003g0080others(1): Show | 4 | HG00609.hp1 NA18945.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-952A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145425 | ||||||
chr4:76145434
|
T | C | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-961A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145434 | ||||||
chr4:76145675
|
A | G | 1 | a0001c0008t0005g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68-1202T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145675 | ||||||
chr4:76145734
|
G | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1261C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145734 | ||||||
chr4:76145761
|
C | G | 3 | a0001c0004t0004g0303a0001c0004t0004g0307a0001c0004t0004g0308 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.68-1288G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145761 | ||||||
chr4:76145980
|
C | T | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.68-1507G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145980 | ||||||
chr4:76145982
|
C | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1509G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145982 | ||||||
chr4:76146012
|
A | G | 1 | a0002c0002t0003g0028 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.68-1539T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146012 | ||||||
chr4:76146177
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1704A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146177 | ||||||
chr4:76146182
|
G | A | 4 | a0001c0004t0004g0302a0001c0004t0004g0305a0001c0004t0004g0306others(1): Show | 4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1709C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146182 | ||||||
chr4:76146215
|
A | G | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.68-1742T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146215 | ||||||
chr4:76146236
|
A | G | 64 | a0001c0001t0004g0008a0001c0001t0004g0014a0001c0001t0004g0015others(61): Show | 69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.68-1763T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146236 | ||||||
chr4:76146246
|
G | T | 1 | a0001c0001t0002g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.68-1773C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146246 | ||||||
chr4:76146272
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.68-1799T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146272 | ||||||
chr4:76146281
|
C | T | 165 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(162): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-1808G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146281 | ||||||
chr4:76146295
|
ATTG | A | 6 | a0001c0001t0004g0224a0001c0001t0004g0225a0001c0001t0004g0226others(3): Show | 6 | NA18964.hp1 NA18971.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-1825_68-1823del others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146295 | ||||||
chr4:76146296
|
T | C | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1823A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146296 | ||||||
chr4:76146330
|
A | G | 65 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(62): Show | 86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-1857T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146330 | ||||||
chr4:76146347
|
A | G | 2 | a0001c0001t0005g0090a0001c0001t0005g0091 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-1874T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146347 | ||||||
chr4:76146489
|
G | C | 2 | a0001c0004t0004g0307a0001c0004t0004g0308 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67+1819C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146489 | ||||||
chr4:76146529
|
G | T | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG00323.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.67+1779C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146529 | ||||||
chr4:76146582
|
GTAAA | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+1722_67+1725del others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146582 | ||||||
chr4:76146638
|
A | G | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+1670T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146638 | ||||||
chr4:76146715
|
C | A | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.67+1593G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146715 | ||||||
chr4:76146837
|
T | A | 1 | a0001c0004t0004g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+1471A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146837 | ||||||
chr4:76146863
|
C | G | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.67+1445G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146863 | ||||||
chr4:76147195
|
C | T | 231 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(228): Show | 266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.67+1113G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147195 | ||||||
chr4:76147214
|
A | ATATAT | 66 | a0002c0002t0003g0001a0002c0002t0003g0002a0002c0002t0003g0005others(63): Show | 87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+1093_67+1094ins others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147214 | ||||||
chr4:76147229
|
T | C | 12 | a0003c0003t0001g0287a0003c0003t0001g0288a0003c0003t0001g0289others(9): Show | 12 | HG01255.hp2 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+1079A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147229 | ||||||
chr4:76147281
|
C | T | 229 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0016others(226): Show | 263 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.67+1027G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147281 | ||||||
chr4:76147409
|
C | T | 1 | a0002c0002t0003g0027 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.67+899G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147409 | ||||||
chr4:76147500
|
C | CAAAATTG others(7): Show |
1 | a0002c0002t0003g0026 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.67+794_67+807dupCT others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147500 | ||||||
chr4:76147733
|
A | G | 2 | a0002c0002t0003g0024a0002c0002t0003g0025 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67+575T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147733 | ||||||
chr4:76147755
|
C | A | 1 | a0001c0001t0002g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67+553G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147755 | ||||||
chr4:76147786
|
A | G | 1 | a0001c0004t0004g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+522T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147786 | ||||||
chr4:76147828
|
T | TA | 15 | a0001c0004t0001g0004a0001c0004t0001g0314a0001c0004t0001g0315others(12): Show | 18 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+479dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147828 | ||||||
chr4:76147889
|
G | C | 1 | a0001c0001t0004g0300 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.67+419C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147889 | ||||||
chr4:76147911
|
C | T | 4 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(1): Show | 4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+397G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147911 | ||||||
chr4:76147943
|
G | A | 68 | a0001c0001t0002g0082a0001c0001t0002g0083a0002c0002t0003g0001others(65): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+365C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147943 | ||||||
chr4:76148060
|
C | G | 68 | a0001c0001t0002g0082a0001c0001t0002g0083a0002c0002t0003g0001others(65): Show | 89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+248G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76148060 | ||||||
chr4:76148101
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.67+207C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76148101 |