geneid | 54888 |
---|---|
ensemblid | ENSG00000037474.15 |
hgncid | 25994 |
symbol | NSUN2 |
name | NOP2/Sun RNA methyltransferase 2 |
refseq_nuc | NM_017755.6 |
refseq_prot | NP_060225.4 |
ensembl_nuc | ENST00000264670.11 |
ensembl_prot | ENSP00000264670.6 |
mane_status | MANE Select |
chr | chr5 |
start | 6599239 |
end | 6633044 |
strand | - |
ver | v1.2 |
region | chr5:6599239-6633044 |
region5000 | chr5:6594239-6638044 |
regionname0 | NSUN2_chr5_6599239_6633044 |
regionname5000 | NSUN2_chr5_6594239_6638044 |
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 | 767 | 389 | 83 | 72 | 176 | 15 | 41 | 133 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002 | 0/0 | 767 | 20 | 8 | 7 | 0 | 1 | 4 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0003 | 0/0 | 767 | 17 | 0 | 0 | 17 | 0 | 0 | 12 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0004 | 0/0 | 767 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0005 | 0/0 | 767 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0006 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0007 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
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 | 1/0 | 2304 | 111 | 43 | 20 | 33 | 8 | 6 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0002 | 0/0 | 2304 | 101 | 4 | 9 | 74 | 1 | 13 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0003 | 0/1 | 2304 | 75 | 14 | 20 | 29 | 3 | 8 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0004 | 0/0 | 2304 | 73 | 9 | 12 | 39 | 2 | 11 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0005 | 0/0 | 2304 | 17 | 0 | 0 | 17 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0006 | 0/0 | 2304 | 8 | 5 | 3 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0007 | 0/0 | 2304 | 8 | 2 | 4 | 0 | 1 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0008 | 0/0 | 2304 | 8 | 7 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0009 | 0/0 | 2304 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0010 | 0/0 | 2304 | 6 | 0 | 5 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0011 | 0/0 | 2304 | 4 | 0 | 1 | 0 | 1 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0012 | 0/0 | 2304 | 4 | 0 | 4 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0013 | 0/0 | 2304 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0014 | 0/0 | 2304 | 3 | 0 | 0 | 0 | 0 | 3 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0015 | 0/0 | 2304 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0016 | 0/0 | 2304 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0017 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0018 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0019 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0020 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
c0021 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
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 | 753 | 340 | 91 | 53 | 150 | 12 | 32 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0002 | 0/0 | 753 | 81 | 3 | 22 | 43 | 3 | 10 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0003 | 0/0 | 752 | 9 | 0 | 6 | 0 | 1 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0004 | 0/0 | 753 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0005 | 0/0 | 753 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0006 | 0/0 | 753 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0007 | 0/0 | 753 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0008 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
t0009 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
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 | 1/0 | 6 | 0 | 0 | 3 | 2 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
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 | 1/0 | 2304 | 111 | 43 | 20 | 33 | 8 | 6 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0002 | 0/0 | 2304 | 101 | 4 | 9 | 74 | 1 | 13 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0003 | 0/1 | 2304 | 75 | 14 | 20 | 29 | 3 | 8 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0004 | 0/0 | 2304 | 73 | 9 | 12 | 39 | 2 | 11 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0009 | 0/0 | 2304 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0010 | 0/0 | 2304 | 6 | 0 | 5 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0011 | 0/0 | 2304 | 4 | 0 | 1 | 0 | 1 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0012 | 0/0 | 2304 | 4 | 0 | 4 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0013 | 0/0 | 2304 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0015 | 0/0 | 2304 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0018 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0019 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0006 | 0/0 | 2304 | 8 | 5 | 3 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0007 | 0/0 | 2304 | 8 | 2 | 4 | 0 | 1 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0014 | 0/0 | 2304 | 3 | 0 | 0 | 0 | 0 | 3 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0017 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0003c0005 | 0/0 | 2304 | 17 | 0 | 0 | 17 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0004c0008 | 0/0 | 2304 | 8 | 7 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0005c0016 | 0/0 | 2304 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0006c0020 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0007c0021 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3056 | 99 | 39 | 17 | 29 | 7 | 6 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0001t0002 | 0/0 | 3056 | 9 | 1 | 3 | 4 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0001t0004 | 0/0 | 3056 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0002t0001 | 0/0 | 3056 | 100 | 4 | 9 | 74 | 1 | 12 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0002t0007 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0003t0001 | 0/1 | 3056 | 73 | 14 | 19 | 28 | 3 | 8 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0003t0002 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0003t0006 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0004t0001 | 0/0 | 3056 | 9 | 7 | 1 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0004t0002 | 0/0 | 3056 | 62 | 2 | 11 | 37 | 2 | 10 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0004t0005 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0004t0008 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0009t0001 | 0/0 | 3056 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0010t0001 | 0/0 | 3056 | 4 | 0 | 3 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0010t0002 | 0/0 | 3056 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0011t0001 | 0/0 | 3056 | 4 | 0 | 1 | 0 | 1 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0012t0002 | 0/0 | 3056 | 4 | 0 | 4 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0013t0001 | 0/0 | 3056 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0015t0001 | 0/0 | 3056 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0018t0001 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0001c0019t0002 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0006t0001 | 0/0 | 3056 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0006t0003 | 0/0 | 3055 | 3 | 0 | 3 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0006t0009 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0007t0001 | 0/0 | 3056 | 4 | 2 | 1 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0007t0003 | 0/0 | 3055 | 4 | 0 | 3 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0014t0001 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0014t0003 | 0/0 | 3055 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0002c0017t0001 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0003c0005t0001 | 0/0 | 3056 | 17 | 0 | 0 | 17 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0004c0008t0001 | 0/0 | 3056 | 8 | 7 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0005c0016t0002 | 0/0 | 3056 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0006c0020t0001 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
a0007c0021t0001 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | copy fasta | chr5 | 6594239 | 6638044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 6 | 0 | 0 | 3 | 2 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0002t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0003t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0004t0008g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0010t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0010t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0010t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0010t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0010t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0010t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0011t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0011t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0011t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0012t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0012t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0012t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0012t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0013t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0013t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0013t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0013t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0015t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0015t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0018t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0001c0019t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0006t0009g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0007t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0007t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0007t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0007t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0007t0003g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0014t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0014t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0014t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0002c0017t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0003c0005t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0004c0008t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0004c0008t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0004c0008t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0004c0008t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0004c0008t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0004c0008t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0005c0016t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0006c0020t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
a0007c0021t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0345 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0298 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00140 | hp2 | a0001 | c0004 | t0002 | g0167 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00280 | hp1 | a0001 | c0004 | t0002 | g0177 | EUR | FIN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0296 | EUR | FIN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00408 | hp2 | a0001 | c0004 | t0002 | g0027 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00423 | hp2 | a0003 | c0005 | t0001 | g0247 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00558 | hp2 | a0003 | c0005 | t0001 | g0257 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00597 | hp1 | a0001 | c0004 | t0002 | g0178 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00609 | hp2 | a0003 | c0005 | t0001 | g0239 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00621 | hp1 | a0001 | c0004 | t0002 | g0175 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00621 | hp2 | a0001 | c0004 | t0002 | g0359 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0107 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00642 | hp2 | a0002 | c0007 | t0003 | g0006 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0364 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0121 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00741 | hp1 | a0001 | c0004 | t0002 | g0202 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01069 | hp1 | a0001 | c0012 | t0002 | g0153 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01070 | hp2 | a0001 | c0004 | t0002 | g0002 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01071 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01071 | hp2 | a0001 | c0012 | t0002 | g0152 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01074 | hp1 | a0001 | c0010 | t0002 | g0105 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01074 | hp2 | a0002 | c0007 | t0001 | g0131 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01099 | hp1 | a0002 | c0007 | t0003 | g0006 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01106 | hp1 | a0002 | c0006 | t0003 | g0094 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01106 | hp2 | a0001 | c0004 | t0002 | g0201 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0111 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01167 | hp1 | a0002 | c0006 | t0003 | g0096 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01168 | hp1 | a0002 | c0007 | t0003 | g0006 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01192 | hp2 | a0001 | c0011 | t0001 | g0045 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01243 | hp1 | a0002 | c0006 | t0003 | g0095 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01243 | hp2 | a0004 | c0008 | t0001 | g0044 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01256 | hp1 | a0001 | c0010 | t0001 | g0058 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01257 | hp1 | a0005 | c0016 | t0002 | g0026 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01257 | hp2 | a0001 | c0010 | t0001 | g0059 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01258 | hp1 | a0005 | c0016 | t0002 | g0026 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0110 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01346 | hp1 | a0001 | c0004 | t0002 | g0024 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0103 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01496 | hp1 | a0001 | c0015 | t0001 | g0087 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01515 | hp1 | a0001 | c0011 | t0001 | g0046 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0020 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0020 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01891 | hp2 | a0001 | c0009 | t0001 | g0047 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01928 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01934 | hp2 | a0001 | c0004 | t0002 | g0024 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01943 | hp2 | a0001 | c0003 | t0006 | g0115 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01952 | hp1 | a0001 | c0004 | t0001 | g0186 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01975 | hp1 | a0001 | c0010 | t0001 | g0060 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01975 | hp2 | a0001 | c0012 | t0002 | g0150 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01978 | hp2 | a0001 | c0012 | t0002 | g0151 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01981 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01993 | hp2 | a0001 | c0004 | t0002 | g0168 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02004 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02015 | hp2 | a0003 | c0005 | t0001 | g0237 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02040 | hp1 | a0001 | c0004 | t0001 | g0160 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02040 | hp2 | a0001 | c0004 | t0002 | g0023 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0203 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02055 | hp2 | a0001 | c0009 | t0001 | g0053 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0097 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02080 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02083 | hp2 | a0003 | c0005 | t0001 | g0270 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02129 | hp1 | a0001 | c0004 | t0002 | g0149 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02132 | hp1 | a0001 | c0004 | t0002 | g0148 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02135 | hp2 | a0001 | c0004 | t0002 | g0196 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0093 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02165 | hp2 | a0001 | c0004 | t0002 | g0189 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02257 | hp2 | a0001 | c0004 | t0002 | g0156 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02258 | hp1 | a0002 | c0006 | t0009 | g0372 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02293 | hp1 | a0001 | c0010 | t0002 | g0119 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0321 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02300 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02451 | hp1 | a0004 | c0008 | t0001 | g0044 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0366 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02572 | hp2 | a0002 | c0006 | t0001 | g0064 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02602 | hp1 | a0001 | c0010 | t0001 | g0057 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02602 | hp2 | a0001 | c0004 | t0002 | g0209 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02615 | hp2 | a0001 | c0009 | t0001 | g0049 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02622 | hp1 | a0004 | c0008 | t0001 | g0043 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02622 | hp2 | a0002 | c0007 | t0001 | g0133 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02630 | hp1 | a0001 | c0013 | t0001 | g0216 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02683 | hp2 | a0002 | c0014 | t0003 | g0246 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0139 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02717 | hp2 | a0002 | c0007 | t0001 | g0129 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02723 | hp1 | a0002 | c0006 | t0001 | g0066 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0154 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02735 | hp1 | a0001 | c0004 | t0002 | g0179 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02735 | hp2 | a0001 | c0011 | t0001 | g0013 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02738 | hp1 | a0001 | c0004 | t0002 | g0198 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02738 | hp2 | a0002 | c0014 | t0003 | g0262 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02809 | hp1 | a0004 | c0008 | t0001 | g0369 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02809 | hp2 | a0001 | c0018 | t0001 | g0137 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02895 | hp1 | a0001 | c0009 | t0001 | g0052 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02897 | hp1 | a0001 | c0009 | t0001 | g0050 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0155 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0092 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0104 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03017 | hp2 | a0001 | c0004 | t0002 | g0206 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03041 | hp1 | a0004 | c0008 | t0001 | g0370 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03195 | hp1 | a0004 | c0008 | t0001 | g0043 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03195 | hp2 | a0001 | c0009 | t0001 | g0051 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03209 | hp1 | a0002 | c0006 | t0001 | g0014 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03209 | hp2 | a0001 | c0013 | t0001 | g0215 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03239 | hp2 | a0002 | c0007 | t0001 | g0132 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03453 | hp1 | a0001 | c0015 | t0001 | g0068 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03486 | hp2 | a0001 | c0009 | t0001 | g0048 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03490 | hp1 | a0006 | c0020 | t0001 | g0282 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03491 | hp2 | a0001 | c0002 | t0007 | g0229 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03688 | hp1 | a0001 | c0011 | t0001 | g0013 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0309 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0099 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0250 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03831 | hp2 | a0001 | c0004 | t0002 | g0023 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03942 | hp1 | a0001 | c0004 | t0002 | g0210 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04115 | hp1 | a0001 | c0004 | t0002 | g0211 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04115 | hp2 | a0001 | c0004 | t0002 | g0195 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0114 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04184 | hp2 | a0001 | c0004 | t0005 | g0176 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04228 | hp1 | a0001 | c0004 | t0002 | g0200 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0117 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18522 | hp1 | a0004 | c0008 | t0001 | g0368 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18522 | hp2 | a0001 | c0013 | t0001 | g0214 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18612 | hp1 | a0001 | c0004 | t0002 | g0358 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18747 | hp1 | a0001 | c0004 | t0002 | g0193 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0144 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18941 | hp1 | a0001 | c0004 | t0002 | g0134 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18943 | hp2 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18944 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18945 | hp1 | a0001 | c0004 | t0002 | g0173 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18945 | hp2 | a0003 | c0005 | t0001 | g0230 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18947 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18950 | hp2 | a0003 | c0005 | t0001 | g0272 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18952 | hp2 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18953 | hp2 | a0001 | c0004 | t0002 | g0197 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18954 | hp2 | a0001 | c0004 | t0002 | g0174 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18956 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18957 | hp1 | a0001 | c0004 | t0002 | g0185 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18962 | hp2 | a0001 | c0004 | t0002 | g0028 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18963 | hp2 | a0001 | c0004 | t0002 | g0170 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18967 | hp1 | a0003 | c0005 | t0001 | g0255 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18968 | hp1 | a0001 | c0004 | t0002 | g0320 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18969 | hp1 | a0003 | c0005 | t0001 | g0234 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18969 | hp2 | a0007 | c0021 | t0001 | g0362 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18970 | hp2 | a0003 | c0005 | t0001 | g0225 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18971 | hp1 | a0001 | c0004 | t0002 | g0135 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18975 | hp1 | a0001 | c0004 | t0002 | g0183 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18980 | hp1 | a0001 | c0019 | t0002 | g0199 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18981 | hp1 | a0003 | c0005 | t0001 | g0287 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18983 | hp2 | a0001 | c0004 | t0002 | g0172 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18988 | hp2 | a0001 | c0004 | t0002 | g0147 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18991 | hp2 | a0001 | c0004 | t0002 | g0140 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18998 | hp1 | a0003 | c0005 | t0001 | g0271 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19001 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19030 | hp1 | a0002 | c0017 | t0001 | g0054 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19056 | hp1 | a0001 | c0004 | t0002 | g0192 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19060 | hp1 | a0001 | c0004 | t0002 | g0181 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19065 | hp1 | a0001 | c0004 | t0002 | g0190 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19068 | hp2 | a0001 | c0004 | t0002 | g0318 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19072 | hp2 | a0003 | c0005 | t0001 | g0227 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19079 | hp1 | a0001 | c0004 | t0008 | g0371 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19080 | hp1 | a0001 | c0004 | t0002 | g0159 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19081 | hp2 | a0003 | c0005 | t0001 | g0248 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19083 | hp1 | a0001 | c0004 | t0002 | g0027 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19089 | hp2 | a0001 | c0004 | t0002 | g0136 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19090 | hp1 | a0001 | c0004 | t0002 | g0028 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19091 | hp2 | a0003 | c0005 | t0001 | g0285 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | ASW | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ASW | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20752 | hp1 | a0002 | c0007 | t0003 | g0006 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0112 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0069 | SAS | GIH | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20905 | hp2 | a0002 | c0014 | t0001 | g0233 | SAS | GIH | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0113 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02109 | hp1 | a0002 | c0006 | t0001 | g0014 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02559 | hp1 | a0004 | c0008 | t0001 | g0367 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA18955 | hp2 | a0001 | c0004 | t0002 | g0319 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0244 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA21309 | hp1 | a0001 | c0013 | t0001 | g0213 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0323 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0108 | REF | REF | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:6599930
|
C | T | 1 | a0005 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.2300G>A | p.Arg767Gln | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2365/3056 | 2300/2304 | 767/767 | chr5 | 6599930 | ||
chr5:6599951
|
G | T | 1 | a0002 | 20 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(17): Show |
missense_variant | MODERATE | c.2279C>A | p.Pro760Gln | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2344/3056 | 2279/2304 | 760/767 | chr5 | 6599951 | ||
chr5:6604216
|
C | T | 1 | a0003 | 17 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(14): Show |
missense_variant | MODERATE | c.1879G>A | p.Val627Ile | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/19 | 1944/3056 | 1879/2304 | 627/767 | chr5 | 6604216 | ||
chr5:6604654
|
C | T | 1 | a0006 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1769G>A | p.Arg590Lys | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/19 | 1834/3056 | 1769/2304 | 590/767 | chr5 | 6604654 | ||
chr5:6631920
|
G | C | 1 | a0007 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.312C>G | p.Asp104Glu | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/19 | 377/3056 | 312/2304 | 104/767 | chr5 | 6631920 | ||
chr5:6632958
|
G | A | 1 | a0004 | 8 | HG01243.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.22C>T | p.Arg8Trp | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 87/3056 | 22/2304 | 8/767 | chr5 | 6632958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:6600007
|
G | A | 1 | a0001c0015 | 2 | HG01496.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2223C>T | p.Pro741Pro | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2288/3056 | 2223/2304 | 741/767 | chr5 | 6600007 | ||
chr5:6600037
|
G | A | 5 | a0001c0004a0001c0010a0001c0011others(2): Show | 88 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
synonymous_variant | LOW | c.2193C>T | p.Asp731Asp | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2258/3056 | 2193/2304 | 731/767 | chr5 | 6600037 | ||
chr5:6604674
|
C | T | 4 | a0001c0002a0002c0014a0003c0005others(1): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
synonymous_variant | LOW | c.1749G>A | p.Thr583Thr | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/19 | 1814/3056 | 1749/2304 | 583/767 | chr5 | 6604674 | ||
chr5:6607250
|
A | G | 1 | a0001c0019 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.1458T>C | p.His486His | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/19 | 1523/3056 | 1458/2304 | 486/767 | chr5 | 6607250 | ||
chr5:6622026
|
G | T | 3 | a0001c0009a0001c0018a0002c0017 | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
synonymous_variant | LOW | c.612C>A | p.Val204Val | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/19 | 677/3056 | 612/2304 | 204/767 | chr5 | 6622026 | ||
chr5:6623241
|
C | T | 1 | a0001c0012 | 4 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(1): Show |
synonymous_variant | LOW | c.510G>A | p.Leu170Leu | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/19 | 575/3056 | 510/2304 | 170/767 | chr5 | 6623241 | ||
chr5:6632730
|
G | A | 1 | a0001c0013 | 4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.123C>T | p.Ile41Ile | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/19 | 188/3056 | 123/2304 | 41/767 | chr5 | 6632730 | ||
chr5:6632929
|
C | T | 6 | a0001c0003a0001c0009a0001c0010others(3): Show | 99 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(96): Show |
synonymous_variant | LOW | c.51G>A | p.Glu17Glu | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 116/3056 | 51/2304 | 17/767 | chr5 | 6632929 | ||
chr5:6632959
|
A | G | 1 | a0001c0011 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
synonymous_variant | LOW | c.21T>C | p.Gly7Gly | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 86/3056 | 21/2304 | 7/767 | chr5 | 6632959 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:6599302
|
T | C | 1 | a0001c0003t0006 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 624 | chr5 | 6599302 | |||||
chr5:6599345
|
A | G | 1 | a0001c0001t0004 | 3 | HG02647.hp1 HG02965.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 581 | chr5 | 6599345 | |||||
chr5:6599363
|
G | A | 1 | a0001c0002t0007 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 563 | chr5 | 6599363 | |||||
chr5:6599379
|
TG | T | 3 | a0002c0006t0003a0002c0007t0003a0002c0014t0003 | 9 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*546delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 546 | chr5 | 6599379 | |||||
chr5:6599704
|
A | G | 1 | a0001c0004t0005 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 222 | chr5 | 6599704 | |||||
chr5:6599827
|
C | T | 9 | a0001c0001t0002a0001c0003t0002a0001c0004t0002others(6): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*99G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 99 | chr5 | 6599827 | |||||
chr5:6633016
|
G | A | 1 | a0001c0004t0008 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 37 | chr5 | 6633016 | |||||
chr5:6633042
|
T | C | 1 | a0002c0006t0009 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 63 | chr5 | 6633042 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:6600276
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1998-44A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600276 | ||||||
chr5:6600379
|
G | GT | 243 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(240): Show | 279 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.1998-148_1998-147i others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600379 | ||||||
chr5:6600384
|
CG | C | 3 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0288 | 3 | NA18965.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1998-153delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600384 | ||||||
chr5:6600385
|
GA | G | 228 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0124others(225): Show | 263 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.1998-154delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600385 | ||||||
chr5:6600490
|
A | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0142others(10): Show | 15 | HG00639.hp2 HG02257.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1998-258T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600490 | ||||||
chr5:6600551
|
C | T | 1 | a0001c0002t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1998-319G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600551 | ||||||
chr5:6600552
|
G | A | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998-320C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600552 | ||||||
chr5:6600559
|
C | G | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998-327G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600559 | ||||||
chr5:6600589
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0165 | 5 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998-357C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600589 | ||||||
chr5:6600654
|
T | TGGGAGAC others(41): Show |
1 | a0001c0001t0002g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1998-470_1998-423d others(50): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600654 | ||||||
chr5:6600654
|
TGGGAGAC others(41): Show |
T | 1 | a0001c0004t0002g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1998-470_1998-423d others(50): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600654 | ||||||
chr5:6600680
|
T | C | 241 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(238): Show | 278 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.1998-448A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600680 | ||||||
chr5:6600751
|
T | C | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1998-519A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600751 | ||||||
chr5:6600891
|
T | C | 110 | a0001c0001t0001g0030a0001c0001t0001g0130a0001c0001t0001g0162others(107): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1998-659A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600891 | ||||||
chr5:6600942
|
A | T | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1998-710T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600942 | ||||||
chr5:6600952
|
G | GT | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998-721_1998-720i others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600952 | ||||||
chr5:6600953
|
C | T | 112 | a0001c0001t0001g0029a0001c0001t0001g0142a0001c0001t0001g0143others(109): Show | 131 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1998-721G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600953 | ||||||
chr5:6600963
|
G | A | 1 | a0001c0011t0001g0046 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1998-731C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600963 | ||||||
chr5:6600966
|
G | A | 1 | a0001c0003t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1998-734C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600966 | ||||||
chr5:6601009
|
T | C | 1 | a0001c0002t0001g0315 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1998-777A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601009 | ||||||
chr5:6601031
|
T | TCTGACCT others(25): Show |
2 | a0001c0009t0001g0053a0002c0017t0001g0054 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1998-831_1998-800d others(34): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601031 | ||||||
chr5:6601057
|
G | A | 2 | a0001c0002t0001g0365a0001c0002t0001g0366 | 2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1998-825C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601057 | ||||||
chr5:6601124
|
T | C | 1 | a0001c0001t0001g0042 | 2 | HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1998-892A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601124 | ||||||
chr5:6601144
|
T | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0126others(24): Show | 31 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1998-912A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601144 | ||||||
chr5:6601163
|
TA | T | 116 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0334others(113): Show | 136 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1998-932delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601163 | ||||||
chr5:6601163
|
TAA | T | 93 | a0001c0001t0001g0041a0001c0001t0001g0124a0001c0001t0001g0141others(90): Show | 104 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1998-933_1998-932d others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601163 | ||||||
chr5:6601163
|
TAAA | T | 112 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0125others(109): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1998-934_1998-932d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601163 | ||||||
chr5:6601196
|
C | T | 319 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(316): Show | 372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.1998-964G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601196 | ||||||
chr5:6601333
|
CA | C | 4 | a0001c0004t0001g0186a0001c0012t0002g0151a0001c0012t0002g0152others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998-1102delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601333 | ||||||
chr5:6601336
|
AC | A | 97 | a0001c0001t0001g0041a0001c0001t0001g0125a0001c0001t0001g0162others(94): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1998-1105delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601336 | ||||||
chr5:6601385
|
C | G | 82 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0162others(79): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1997+1076G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601385 | ||||||
chr5:6601570
|
C | G | 3 | a0001c0001t0001g0220a0001c0003t0001g0098a0002c0006t0009g0372 | 3 | HG02258.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1997+891G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601570 | ||||||
chr5:6601586
|
C | A | 27 | a0001c0001t0001g0275a0001c0001t0001g0333a0001c0003t0001g0016others(24): Show | 31 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1997+875G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601586 | ||||||
chr5:6601600
|
A | ATCCC | 160 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0130others(157): Show | 186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1997+857_1997+860d others(6): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601600 | ||||||
chr5:6601606
|
C | T | 1 | a0001c0003t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1997+855G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601606 | ||||||
chr5:6601687
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1997+774C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601687 | ||||||
chr5:6601830
|
C | T | 1 | a0001c0009t0001g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1997+631G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601830 | ||||||
chr5:6601831
|
G | A | 2 | a0003c0005t0001g0271a0003c0005t0001g0272 | 2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1997+630C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601831 | ||||||
chr5:6601910
|
G | A | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1997+551C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601910 | ||||||
chr5:6602040
|
G | A | 1 | a0001c0001t0001g0352 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1997+421C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602040 | ||||||
chr5:6602162
|
C | T | 5 | a0001c0003t0001g0007a0001c0003t0001g0116a0001c0003t0001g0117others(2): Show | 7 | HG01943.hp2 HG01993.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1997+299G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602162 | ||||||
chr5:6602259
|
T | TGAGTGTT others(147): Show |
2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1997+201_1997+202i others(156): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602259 | ||||||
chr5:6602314
|
G | T | 1 | a0001c0003t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1997+147C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602314 | ||||||
chr5:6602431
|
T | C | 251 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(248): Show | 288 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.1997+30A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602431 | ||||||
chr5:6602432
|
G | A | 2 | a0001c0002t0007g0229a0001c0003t0001g0121 | 2 | HG00735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1997+29C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602432 | ||||||
chr5:6602555
|
G | C | 116 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(113): Show | 132 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1958-55C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602555 | ||||||
chr5:6602581
|
T | C | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-81A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602581 | ||||||
chr5:6602693
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1958-193T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602693 | ||||||
chr5:6602698
|
G | A | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-198C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602698 | ||||||
chr5:6602730
|
A | G | 2 | a0001c0002t0001g0250a0001c0002t0001g0261 | 2 | HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1958-230T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602730 | ||||||
chr5:6602806
|
T | C | 1 | a0001c0002t0001g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1958-306A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602806 | ||||||
chr5:6602865
|
C | T | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1958-365G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602865 | ||||||
chr5:6602887
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1958-387T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602887 | ||||||
chr5:6603104
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1958-604G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603104 | ||||||
chr5:6603110
|
G | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1958-610C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603110 | ||||||
chr5:6603159
|
A | C | 1 | a0001c0004t0001g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1958-659T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603159 | ||||||
chr5:6603220
|
G | A | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1958-720C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603220 | ||||||
chr5:6603400
|
C | G | 1 | a0001c0013t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1957+738G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603400 | ||||||
chr5:6603430
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1957+708C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603430 | ||||||
chr5:6603552
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0163others(8): Show | 14 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1957+586C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603552 | ||||||
chr5:6603566
|
T | C | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957+572A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603566 | ||||||
chr5:6603598
|
G | A | 122 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(119): Show | 138 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1957+540C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603598 | ||||||
chr5:6603599
|
G | T | 1 | a0001c0002t0007g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1957+539C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603599 | ||||||
chr5:6603625
|
G | C | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+513C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603625 | ||||||
chr5:6603638
|
C | T | 1 | a0001c0004t0002g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1957+500G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603638 | ||||||
chr5:6603751
|
G | A | 1 | a0001c0003t0001g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1957+387C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603751 | ||||||
chr5:6603829
|
C | T | 116 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(113): Show | 132 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1957+309G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603829 | ||||||
chr5:6603833
|
G | A | 1 | a0001c0004t0002g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1957+305C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603833 | ||||||
chr5:6603925
|
A | G | 1 | a0001c0013t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1957+213T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603925 | ||||||
chr5:6604026
|
A | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957+112T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6604026 | ||||||
chr5:6604092
|
A | G | 120 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0267others(117): Show | 141 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1957+46T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6604092 | ||||||
chr5:6604329
|
G | A | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1819-53C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604329 | ||||||
chr5:6604420
|
AC | A | 245 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(242): Show | 282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1819-145delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604420 | ||||||
chr5:6604427
|
C | G | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1819-151G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604427 | ||||||
chr5:6604451
|
G | A | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1818+154C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604451 | ||||||
chr5:6604752
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1738-67C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604752 | ||||||
chr5:6604818
|
C | T | 208 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(205): Show | 240 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1738-133G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604818 | ||||||
chr5:6604829
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1738-144G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604829 | ||||||
chr5:6604830
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1738-145C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604830 | ||||||
chr5:6604839
|
C | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(25): Show | 33 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1738-154G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604839 | ||||||
chr5:6604857
|
G | A | 202 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(199): Show | 234 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1738-172C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604857 | ||||||
chr5:6604858
|
T | C | 1 | a0001c0002t0001g0286 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1738-173A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604858 | ||||||
chr5:6604899
|
A | T | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-214T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604899 | ||||||
chr5:6604963
|
G | A | 1 | a0001c0003t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1738-278C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604963 | ||||||
chr5:6605158
|
G | A | 261 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(258): Show | 301 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.1737+115C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605158 | ||||||
chr5:6605176
|
G | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1737+97C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605176 | ||||||
chr5:6605212
|
C | T | 1 | a0001c0002t0001g0309 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1737+61G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605212 | ||||||
chr5:6605227
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG00544.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1737+46G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605227 | ||||||
chr5:6605256
|
G | A | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+17C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605256 | ||||||
chr5:6605419
|
C | A | 250 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(247): Show | 287 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.1602-11G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605419 | ||||||
chr5:6605422
|
CATT | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602-17_1602-15del others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605422 | ||||||
chr5:6605427
|
T | C | 4 | a0001c0003t0001g0104a0001c0003t0001g0107a0001c0003t0001g0113others(1): Show | 4 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602-19A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605427 | ||||||
chr5:6605566
|
T | G | 1 | a0001c0004t0002g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1602-158A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605566 | ||||||
chr5:6605658
|
C | T | 1 | a0001c0004t0002g0135 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1602-250G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605658 | ||||||
chr5:6605716
|
G | T | 90 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(87): Show | 104 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1602-308C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605716 | ||||||
chr5:6605720
|
T | C | 2 | a0003c0005t0001g0234a0003c0005t0001g0247 | 2 | HG00423.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1602-312A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605720 | ||||||
chr5:6605823
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1602-415A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605823 | ||||||
chr5:6605857
|
AT | A | 202 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(199): Show | 234 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1602-450delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605857 | ||||||
chr5:6605906
|
A | G | 208 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(205): Show | 240 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1602-498T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605906 | ||||||
chr5:6605975
|
T | A | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-567A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605975 | ||||||
chr5:6606180
|
T | C | 1 | a0001c0002t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1601+640A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606180 | ||||||
chr5:6606190
|
C | T | 202 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(199): Show | 234 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1601+630G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606190 | ||||||
chr5:6606210
|
T | C | 245 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(242): Show | 282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1601+610A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606210 | ||||||
chr5:6606332
|
G | A | 90 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(87): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1601+488C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606332 | ||||||
chr5:6606342
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1601+478C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606342 | ||||||
chr5:6606362
|
C | A | 34 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(31): Show | 39 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1601+458G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606362 | ||||||
chr5:6606440
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1601+380G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606440 | ||||||
chr5:6606441
|
G | A | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+379C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606441 | ||||||
chr5:6606531
|
C | T | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+289G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606531 | ||||||
chr5:6606574
|
C | T | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(25): Show | 33 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1601+246G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606574 | ||||||
chr5:6606587
|
G | GT | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1601+232dupA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606587 | ||||||
chr5:6606618
|
A | G | 3 | a0001c0004t0002g0170a0001c0004t0002g0185a0001c0004t0002g0196 | 3 | HG02135.hp2 NA18957.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1601+202T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606618 | ||||||
chr5:6606633
|
CTTAAA | C | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+182_1601+186d others(7): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606633 | ||||||
chr5:6606694
|
G | A | 92 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(89): Show | 106 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1601+126C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606694 | ||||||
chr5:6606697
|
TA | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0162others(11): Show | 17 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1601+122delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606697 | ||||||
chr5:6606697
|
TAA | T | 34 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(31): Show | 39 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1601+121_1601+122d others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606697 | ||||||
chr5:6606697
|
TAAA | T | 200 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(197): Show | 232 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.1601+120_1601+122d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606697 | ||||||
chr5:6607009
|
A | G | 1 | a0001c0010t0002g0119 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1509-97T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607009 | ||||||
chr5:6607012
|
GAAC | G | 245 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(242): Show | 282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1509-103_1509-101d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607012 | ||||||
chr5:6607022
|
C | T | 35 | a0001c0001t0001g0232a0001c0001t0001g0275a0001c0001t0001g0276others(32): Show | 40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1509-110G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607022 | ||||||
chr5:6607031
|
T | C | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509-119A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607031 | ||||||
chr5:6607042
|
C | T | 3 | a0001c0001t0004g0138a0001c0001t0004g0208a0001c0001t0004g0323 | 3 | HG02647.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1509-130G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607042 | ||||||
chr5:6607110
|
C | T | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1508+90G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607110 | ||||||
chr5:6607416
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1324-32T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607416 | ||||||
chr5:6607495
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1324-111G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607495 | ||||||
chr5:6607504
|
T | G | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-120A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607504 | ||||||
chr5:6607627
|
T | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324-243A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607627 | ||||||
chr5:6607803
|
T | C | 245 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(242): Show | 282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1324-419A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607803 | ||||||
chr5:6607837
|
AG | A | 5 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-454delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607837 | ||||||
chr5:6607935
|
T | C | 4 | a0002c0006t0003g0094a0002c0006t0003g0095a0002c0006t0003g0096others(1): Show | 7 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1324-551A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607935 | ||||||
chr5:6607943
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(24): Show | 32 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1324-559C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607943 | ||||||
chr5:6607986
|
TTTTTAAC others(1): Show |
T | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-610_1324-603d others(10): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607986 | ||||||
chr5:6608037
|
T | C | 209 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(206): Show | 241 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.1324-653A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608037 | ||||||
chr5:6608223
|
G | C | 3 | a0001c0002t0001g0226a0001c0002t0001g0254a0001c0002t0001g0364 | 3 | HG00673.hp1 NA18941.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1324-839C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608223 | ||||||
chr5:6608228
|
C | A | 16 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(13): Show | 19 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1324-844G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608228 | ||||||
chr5:6608248
|
C | A | 105 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(102): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1324-864G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608248 | ||||||
chr5:6608317
|
T | C | 1 | a0001c0004t0002g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1324-933A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608317 | ||||||
chr5:6608326
|
A | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324-942T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608326 | ||||||
chr5:6608421
|
A | T | 261 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(258): Show | 301 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.1324-1037T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608421 | ||||||
chr5:6608516
|
A | G | 40 | a0001c0001t0001g0232a0001c0001t0001g0275a0001c0001t0001g0276others(37): Show | 45 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1324-1132T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608516 | ||||||
chr5:6608609
|
A | C | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1217T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608609 | ||||||
chr5:6608670
|
A | G | 1 | a0001c0003t0001g0073 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1323+1156T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608670 | ||||||
chr5:6608676
|
G | A | 1 | a0001c0002t0001g0315 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1323+1150C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608676 | ||||||
chr5:6608764
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(338): Show | 397 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(394): Show |
intron_variant | MODIFIER | c.1323+1062T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608764 | ||||||
chr5:6608844
|
T | C | 207 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(204): Show | 239 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1323+982A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608844 | ||||||
chr5:6608911
|
C | T | 31 | a0001c0003t0001g0007a0001c0003t0001g0020a0001c0003t0001g0021others(28): Show | 35 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1323+915G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608911 | ||||||
chr5:6608912
|
G | A | 2 | a0001c0004t0002g0140a0001c0004t0002g0192 | 2 | NA18991.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1323+914C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608912 | ||||||
chr5:6608953
|
C | T | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+873G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608953 | ||||||
chr5:6608975
|
C | A | 153 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0001g0145others(150): Show | 180 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1323+851G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608975 | ||||||
chr5:6608979
|
G | A | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+847C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608979 | ||||||
chr5:6608999
|
G | A | 157 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0001g0145others(154): Show | 184 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1323+827C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608999 | ||||||
chr5:6609001
|
C | A | 11 | a0001c0001t0001g0126a0001c0001t0001g0143a0001c0009t0001g0047others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1323+825G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609001 | ||||||
chr5:6609011
|
C | T | 1 | a0001c0002t0001g0307 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1323+815G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609011 | ||||||
chr5:6609025
|
C | T | 2 | a0001c0003t0001g0063a0001c0003t0001g0092 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1323+801G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609025 | ||||||
chr5:6609026
|
G | A | 198 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0001g0145others(195): Show | 230 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1323+800C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609026 | ||||||
chr5:6609051
|
G | A | 2 | a0001c0001t0004g0138a0001c0001t0004g0208 | 2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1323+775C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609051 | ||||||
chr5:6609157
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1323+669G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609157 | ||||||
chr5:6609246
|
G | A | 1 | a0001c0004t0002g0193 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1323+580C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609246 | ||||||
chr5:6609283
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1323+543C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609283 | ||||||
chr5:6609315
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1323+511G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609315 | ||||||
chr5:6609401
|
G | A | 1 | a0001c0004t0001g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1323+425C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609401 | ||||||
chr5:6609760
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1323+66G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609760 | ||||||
chr5:6610054
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227-132A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610054 | ||||||
chr5:6610065
|
A | AT | 10 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(7): Show | 11 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1227-144dupA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610065 | ||||||
chr5:6610065
|
A | ATT | 8 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227-145_1227-144d others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610065 | ||||||
chr5:6610065
|
AT | A | 32 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(29): Show | 35 | HG00140.hp1 HG01074.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1227-144delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610065 | ||||||
chr5:6610082
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1227-160C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610082 | ||||||
chr5:6610124
|
T | C | 208 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(205): Show | 240 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1227-202A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610124 | ||||||
chr5:6610124
|
T | G | 1 | a0004c0008t0001g0044 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1227-202A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610124 | ||||||
chr5:6610127
|
G | A | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227-205C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610127 | ||||||
chr5:6610136
|
C | T | 217 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(214): Show | 249 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1227-214G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610136 | ||||||
chr5:6610149
|
C | T | 3 | a0001c0001t0004g0138a0001c0001t0004g0208a0001c0001t0004g0323 | 3 | HG02647.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1227-227G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610149 | ||||||
chr5:6610150
|
G | A | 208 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(205): Show | 240 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1227-228C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610150 | ||||||
chr5:6610199
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1227-277C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610199 | ||||||
chr5:6610224
|
T | G | 2 | a0001c0003t0001g0101a0001c0003t0001g0102 | 2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1227-302A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610224 | ||||||
chr5:6610238
|
A | G | 1 | a0001c0003t0001g0015 | 2 | NA19001.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1227-316T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610238 | ||||||
chr5:6610246
|
T | TC | 4 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 7 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1227-325_1227-324i others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610246 | ||||||
chr5:6610278
|
T | C | 245 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(242): Show | 282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1227-356A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610278 | ||||||
chr5:6610332
|
C | T | 1 | a0001c0003t0001g0017 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1227-410G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610332 | ||||||
chr5:6610363
|
C | T | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227-441G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610363 | ||||||
chr5:6610613
|
G | A | 1 | a0001c0001t0004g0323 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1226+342C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610613 | ||||||
chr5:6610673
|
G | T | 202 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(199): Show | 234 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1226+282C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610673 | ||||||
chr5:6610683
|
CA | C | 198 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0001g0145others(195): Show | 230 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.1226+271delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610683 | ||||||
chr5:6610755
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1226+200T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610755 | ||||||
chr5:6610785
|
G | A | 1 | a0001c0004t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1226+170C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610785 | ||||||
chr5:6610798
|
T | C | 92 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(89): Show | 106 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1226+157A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610798 | ||||||
chr5:6610951
|
T | A | 1 | a0001c0002t0001g0236 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.1226+4A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610951 | ||||||
chr5:6611102
|
T | C | 16 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0031others(13): Show | 22 | HG00438.hp2 HG00673.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.1096-17A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611102 | ||||||
chr5:6611155
|
G | A | 1 | a0002c0007t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1096-70C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611155 | ||||||
chr5:6611252
|
A | G | 2 | a0001c0004t0002g0135a0001c0004t0002g0136 | 2 | NA18971.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1096-167T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611252 | ||||||
chr5:6611448
|
T | TA | 9 | a0001c0003t0001g0022a0001c0003t0001g0067a0001c0003t0001g0122others(6): Show | 12 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1095+276dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAA | 89 | a0001c0001t0001g0267a0001c0002t0001g0005a0001c0002t0001g0009others(86): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1095+271_1095+276d others(8): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA | 17 | a0001c0002t0001g0037a0001c0002t0001g0039a0001c0002t0001g0212others(14): Show | 19 | HG02056.hp2 HG02523.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+270_1095+276d others(9): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(3): Show |
1 | a0004c0008t0001g0369 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1095+267_1095+276d others(12): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(4): Show |
16 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(13): Show | 19 | HG00423.hp1 HG01074.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+266_1095+276d others(13): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(7): Show |
1 | a0001c0003t0001g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1095+263_1095+276d others(16): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(8): Show |
17 | a0001c0001t0001g0127a0001c0001t0001g0145a0001c0001t0001g0146others(14): Show | 19 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+262_1095+276d others(17): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(9): Show |
16 | a0001c0001t0001g0276a0001c0003t0001g0070a0001c0003t0001g0071others(13): Show | 16 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+261_1095+276d others(18): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(10): Show |
23 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(20): Show | 26 | HG01109.hp1 HG01261.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1095+260_1095+276d others(19): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(11): Show |
13 | a0001c0001t0001g0041a0001c0001t0001g0232a0001c0001t0001g0280others(10): Show | 15 | HG00408.hp1 HG00597.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+276_1095+277i others(20): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(12): Show |
9 | a0001c0001t0001g0275a0001c0001t0001g0325a0001c0001t0001g0327others(6): Show | 12 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+276_1095+277i others(21): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(13): Show |
6 | a0001c0001t0001g0330a0001c0001t0001g0332a0001c0001t0004g0138others(3): Show | 6 | HG00735.hp1 HG01952.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+276_1095+277i others(22): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0004g0323 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1095+276_1095+277i others(23): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
T | TAAAAAAA others(15): Show |
1 | a0001c0003t0001g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1095+276_1095+277i others(24): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
TA | T | 6 | a0001c0001t0001g0341a0001c0004t0002g0168a0002c0006t0003g0094others(3): Show | 9 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1095+276delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
TAAA | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1095+274_1095+276d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611448
|
TAAAAAAA others(2): Show |
T | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1095+268_1095+276d others(11): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | ||||||
chr5:6611519
|
G | GA | 10 | a0001c0002t0001g0265a0001c0009t0001g0047a0001c0009t0001g0048others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+205dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611519 | ||||||
chr5:6611520
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1095+205T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611520 | ||||||
chr5:6611528
|
A | C | 1 | a0001c0004t0002g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1095+197T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611528 | ||||||
chr5:6611644
|
A | T | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1095+81T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611644 | ||||||
chr5:6611712
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1095+13C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611712 | ||||||
chr5:6611870
|
C | A | 202 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(199): Show | 234 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1022-72G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611870 | ||||||
chr5:6611914
|
T | C | 88 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(85): Show | 99 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1022-116A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611914 | ||||||
chr5:6611935
|
G | A | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-137C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611935 | ||||||
chr5:6611956
|
C | T | 24 | a0001c0003t0001g0020a0001c0003t0001g0021a0001c0003t0001g0056others(21): Show | 26 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1022-158G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611956 | ||||||
chr5:6611960
|
G | A | 1 | a0004c0008t0001g0044 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1022-162C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611960 | ||||||
chr5:6612083
|
G | A | 1 | a0001c0001t0001g0354 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1022-285C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612083 | ||||||
chr5:6612130
|
A | G | 220 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(217): Show | 252 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.1022-332T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612130 | ||||||
chr5:6612259
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 9 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-461C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612259 | ||||||
chr5:6612272
|
A | G | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-474T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612272 | ||||||
chr5:6612293
|
G | A | 4 | a0001c0003t0001g0019a0001c0003t0001g0088a0001c0003t0001g0089others(1): Show | 5 | NA18940.hp1 NA18942.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-495C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612293 | ||||||
chr5:6612311
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-513T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612311 | ||||||
chr5:6612319
|
CA | C | 6 | a0001c0001t0001g0267a0001c0003t0001g0062a0001c0003t0001g0065others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-522delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612319 | ||||||
chr5:6612351
|
A | G | 261 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(258): Show | 301 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.1022-553T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612351 | ||||||
chr5:6612409
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1022-611C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612409 | ||||||
chr5:6612540
|
C | A | 5 | a0001c0003t0001g0098a0001c0013t0001g0213a0001c0013t0001g0214others(2): Show | 5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-742G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612540 | ||||||
chr5:6612557
|
G | A | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-759C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612557 | ||||||
chr5:6612557
|
G | C | 1 | a0001c0004t0001g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1022-759C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612557 | ||||||
chr5:6612662
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-864C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612662 | ||||||
chr5:6612767
|
C | T | 4 | a0001c0001t0002g0184a0001c0001t0002g0194a0001c0004t0002g0183others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-969G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612767 | ||||||
chr5:6612782
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1022-984T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612782 | ||||||
chr5:6612793
|
G | C | 16 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(13): Show | 19 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022-995C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612793 | ||||||
chr5:6612796
|
G | A | 4 | a0002c0006t0003g0094a0002c0006t0003g0095a0002c0006t0003g0096others(1): Show | 7 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-998C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612796 | ||||||
chr5:6612866
|
A | G | 1 | a0001c0001t0002g0182 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1022-1068T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612866 | ||||||
chr5:6612873
|
C | A | 1 | a0001c0002t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1022-1075G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612873 | ||||||
chr5:6613030
|
G | C | 1 | a0001c0012t0002g0150 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1022-1232C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613030 | ||||||
chr5:6613033
|
A | G | 211 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(208): Show | 243 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.1022-1235T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613033 | ||||||
chr5:6613045
|
G | C | 5 | a0001c0002t0001g0038a0001c0002t0001g0304a0001c0002t0001g0305others(2): Show | 6 | NA18942.hp2 NA18948.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-1247C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613045 | ||||||
chr5:6613305
|
G | A | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1022-1507C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613305 | ||||||
chr5:6613404
|
C | T | 105 | a0001c0002t0001g0005a0001c0002t0001g0009a0001c0002t0001g0010others(102): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1022-1606G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613404 | ||||||
chr5:6613456
|
G | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-1658C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613456 | ||||||
chr5:6613571
|
G | A | 1 | a0001c0004t0002g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1022-1773C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613571 | ||||||
chr5:6613641
|
G | A | 4 | a0002c0006t0003g0094a0002c0006t0003g0095a0002c0006t0003g0096others(1): Show | 7 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-1843C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613641 | ||||||
chr5:6613706
|
G | A | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-1908C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613706 | ||||||
chr5:6613709
|
C | A | 1 | a0001c0002t0001g0266 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1022-1911G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613709 | ||||||
chr5:6613714
|
T | C | 239 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(236): Show | 276 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.1022-1916A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613714 | ||||||
chr5:6613821
|
G | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0204others(2): Show | 5 | HG02258.hp2 HG06807.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-2023C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613821 | ||||||
chr5:6613889
|
G | C | 1 | a0001c0002t0001g0235 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1022-2091C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613889 | ||||||
chr5:6613922
|
C | A | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-2124G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613922 | ||||||
chr5:6614053
|
G | A | 2 | a0001c0001t0004g0138a0001c0001t0004g0208 | 2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1022-2255C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614053 | ||||||
chr5:6614093
|
CG | C | 7 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0050others(4): Show | 7 | HG01891.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-2296delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614093 | ||||||
chr5:6614095
|
G | A | 236 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(233): Show | 273 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.1022-2297C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614095 | ||||||
chr5:6614095
|
G | GA | 57 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0336others(54): Show | 69 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1022-2298dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614095 | ||||||
chr5:6614095
|
GA | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 9 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-2298delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614095 | ||||||
chr5:6614110
|
A | C | 12 | a0001c0003t0001g0055a0002c0006t0001g0014a0002c0007t0001g0129others(9): Show | 15 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1022-2312T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614110 | ||||||
chr5:6614111
|
A | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(1): Show | 4 | HG01891.hp1 HG02698.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-2313T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614111 | ||||||
chr5:6614119
|
A | ACCCTCC | 124 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0145others(121): Show | 147 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1022-2322_1022-232 others(10): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614119 | ||||||
chr5:6614119
|
A | C | 15 | a0001c0001t0004g0138a0001c0002t0001g0273a0001c0003t0001g0097others(12): Show | 18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2321T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614119 | ||||||
chr5:6614120
|
A | ACCCTCCC | 61 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0141others(58): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1022-2323_1022-232 others(11): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614120 | ||||||
chr5:6614120
|
A | C | 139 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0145others(136): Show | 165 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1022-2322T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614120 | ||||||
chr5:6614121
|
A | C | 15 | a0001c0001t0004g0138a0001c0002t0001g0273a0001c0003t0001g0097others(12): Show | 18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2323T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614121 | ||||||
chr5:6614122
|
A | C | 221 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(218): Show | 255 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.1022-2324T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614122 | ||||||
chr5:6614122
|
A | T | 15 | a0001c0001t0004g0138a0001c0002t0001g0273a0001c0003t0001g0097others(12): Show | 18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2324T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614122 | ||||||
chr5:6614124
|
C | CCTCCCAC others(2): Show |
9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(6): Show | 9 | HG01109.hp2 HG01123.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1022-2327_1022-232 others(13): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614124 | ||||||
chr5:6614124
|
C | CTCCCACC others(1): Show |
36 | a0001c0001t0001g0030a0001c0001t0001g0142a0001c0001t0001g0143others(33): Show | 42 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1022-2327_1022-232 others(12): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614124 | ||||||
chr5:6614124
|
C | T | 185 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0126others(182): Show | 213 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1022-2326G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614124 | ||||||
chr5:6614127
|
C | CCTCA | 15 | a0001c0001t0004g0138a0001c0002t0001g0273a0001c0003t0001g0097others(12): Show | 18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2330_1022-232 others(8): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614127 | ||||||
chr5:6614128
|
A | C | 15 | a0001c0001t0004g0138a0001c0002t0001g0273a0001c0003t0001g0097others(12): Show | 18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2330T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614128 | ||||||
chr5:6614129
|
AC | A | 230 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(227): Show | 264 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.1022-2332delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614129 | ||||||
chr5:6614130
|
C | A | 15 | a0001c0001t0004g0138a0001c0002t0001g0273a0001c0003t0001g0097others(12): Show | 18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2332G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614130 | ||||||
chr5:6614200
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1022-2402G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614200 | ||||||
chr5:6614311
|
C | A | 1 | a0001c0004t0002g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1021+2416G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614311 | ||||||
chr5:6614462
|
C | A | 1 | a0001c0003t0001g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1021+2265G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614462 | ||||||
chr5:6614467
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+2260C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614467 | ||||||
chr5:6614540
|
G | C | 211 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(208): Show | 243 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.1021+2187C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614540 | ||||||
chr5:6614542
|
T | C | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1021+2185A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614542 | ||||||
chr5:6614651
|
C | T | 208 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(205): Show | 240 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1021+2076G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614651 | ||||||
chr5:6614767
|
T | G | 1 | a0001c0004t0002g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1021+1960A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614767 | ||||||
chr5:6614850
|
G | A | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1021+1877C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614850 | ||||||
chr5:6614850
|
G | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021+1877C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614850 | ||||||
chr5:6614856
|
A | G | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1021+1871T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614856 | ||||||
chr5:6614947
|
A | C | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1021+1780T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614947 | ||||||
chr5:6614979
|
A | C | 205 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(202): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1021+1748T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614979 | ||||||
chr5:6615042
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01255.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+1685G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615042 | ||||||
chr5:6615275
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 9 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021+1452T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615275 | ||||||
chr5:6615388
|
C | A | 3 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0288 | 3 | NA18965.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1021+1339G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615388 | ||||||
chr5:6615430
|
T | C | 221 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0126others(218): Show | 251 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.1021+1297A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615430 | ||||||
chr5:6615510
|
T | C | 1 | a0002c0006t0003g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1021+1217A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615510 | ||||||
chr5:6615516
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1021+1211A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615516 | ||||||
chr5:6615615
|
GC | G | 253 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(250): Show | 290 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1021+1111delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615615 | ||||||
chr5:6615627
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0324a0001c0001t0001g0325others(7): Show | 11 | HG01261.hp2 HG01884.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021+1100G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615627 | ||||||
chr5:6615878
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021+849C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615878 | ||||||
chr5:6615884
|
C | A | 1 | a0002c0006t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1021+843G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615884 | ||||||
chr5:6615991
|
A | G | 12 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0128others(9): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+736T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615991 | ||||||
chr5:6616107
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1021+620G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616107 | ||||||
chr5:6616121
|
A | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0145others(55): Show | 65 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.1021+606T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616121 | ||||||
chr5:6616141
|
T | C | 1 | a0001c0002t0001g0269 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1021+586A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616141 | ||||||
chr5:6616164
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(181): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1021+563T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616164 | ||||||
chr5:6616214
|
C | G | 1 | a0001c0002t0001g0290 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1021+513G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616214 | ||||||
chr5:6616253
|
G | C | 1 | a0001c0004t0002g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1021+474C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616253 | ||||||
chr5:6616270
|
G | A | 2 | a0001c0003t0001g0021a0001c0003t0001g0111 | 3 | HG00735.hp2 HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1021+457C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616270 | ||||||
chr5:6616290
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1021+437C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616290 | ||||||
chr5:6616295
|
T | C | 186 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0161others(183): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1021+432A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616295 | ||||||
chr5:6616419
|
T | C | 230 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0124others(227): Show | 266 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.1021+308A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616419 | ||||||
chr5:6616455
|
G | T | 2 | a0001c0002t0001g0291a0001c0002t0001g0292 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1021+272C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616455 | ||||||
chr5:6616623
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+104G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616623 | ||||||
chr5:6616669
|
CAT | C | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.1021+56_1021+57del others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616669 | ||||||
chr5:6616675
|
C | A | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.1021+52G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616675 | ||||||
chr5:6616676
|
A | T | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.1021+51T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616676 | ||||||
chr5:6616678
|
A | AAAAATTT others(237): Show |
1 | a0001c0002t0001g0300 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1021+48_1021+49ins others(244): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616678 | ||||||
chr5:6616678
|
A | AAAAATTT others(238): Show |
246 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(243): Show | 283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1021+48_1021+49ins others(245): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616678 | ||||||
chr5:6616681
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021+46T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616681 | ||||||
chr5:6616886
|
G | C | 3 | a0001c0001t0001g0275a0001c0002t0001g0273a0001c0002t0001g0274 | 3 | HG00438.hp1 HG00544.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.891-29C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6616886 | ||||||
chr5:6616898
|
C | A | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.891-41G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6616898 | ||||||
chr5:6617044
|
AT | A | 5 | a0001c0003t0001g0062a0001c0003t0001g0065a0002c0006t0001g0064others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.891-188delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617044 | ||||||
chr5:6617108
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891-251T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617108 | ||||||
chr5:6617368
|
C | T | 116 | a0001c0001t0001g0232a0001c0001t0001g0267a0001c0001t0001g0275others(113): Show | 133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.891-511G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617368 | ||||||
chr5:6617429
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.890+521T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617429 | ||||||
chr5:6617498
|
C | T | 3 | a0001c0004t0002g0002a0001c0004t0002g0024a0001c0004t0002g0168 | 8 | HG01070.hp2 HG01071.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.890+452G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617498 | ||||||
chr5:6617601
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890+349G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617601 | ||||||
chr5:6618073
|
T | C | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.816-49A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618073 | ||||||
chr5:6618210
|
G | C | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.816-186C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618210 | ||||||
chr5:6618302
|
G | A | 1 | a0001c0002t0001g0290 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.816-278C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618302 | ||||||
chr5:6618317
|
A | C | 5 | a0001c0003t0001g0062a0001c0003t0001g0065a0002c0006t0001g0064others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-293T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618317 | ||||||
chr5:6618334
|
T | C | 5 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0204others(2): Show | 5 | HG02258.hp2 HG06807.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-310A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618334 | ||||||
chr5:6618546
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816-522A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618546 | ||||||
chr5:6618590
|
T | C | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.816-566A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618590 | ||||||
chr5:6618643
|
T | C | 83 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(80): Show | 94 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.816-619A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618643 | ||||||
chr5:6618761
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.816-737T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618761 | ||||||
chr5:6618839
|
G | A | 6 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0061others(3): Show | 8 | HG00673.hp2 NA18940.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.816-815C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618839 | ||||||
chr5:6618882
|
A | G | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-858T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618882 | ||||||
chr5:6618896
|
T | G | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-872A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618896 | ||||||
chr5:6618903
|
G | A | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-879C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618903 | ||||||
chr5:6619105
|
G | A | 1 | a0001c0002t0007g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.815+1001C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619105 | ||||||
chr5:6619167
|
A | T | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.815+939T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619167 | ||||||
chr5:6619182
|
T | C | 1 | a0001c0004t0002g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.815+924A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619182 | ||||||
chr5:6619265
|
G | A | 3 | a0001c0010t0001g0058a0001c0010t0001g0059a0001c0010t0001g0060 | 3 | HG01256.hp1 HG01257.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.815+841C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619265 | ||||||
chr5:6619351
|
G | A | 3 | a0002c0006t0003g0094a0002c0006t0003g0095a0002c0006t0003g0096 | 3 | HG01106.hp1 HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.815+755C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619351 | ||||||
chr5:6619458
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.815+648G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619458 | ||||||
chr5:6619587
|
T | C | 3 | a0001c0002t0001g0040a0001c0002t0001g0316a0001c0002t0001g0317 | 4 | HG00609.hp1 NA18991.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.815+519A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619587 | ||||||
chr5:6619620
|
C | T | 252 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(249): Show | 289 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.815+486G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619620 | ||||||
chr5:6619766
|
G | A | 5 | a0001c0003t0001g0062a0001c0003t0001g0065a0002c0006t0001g0064others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+340C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619766 | ||||||
chr5:6619785
|
A | G | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.815+321T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619785 | ||||||
chr5:6619797
|
AACAC | A | 5 | a0001c0003t0001g0062a0001c0003t0001g0065a0002c0006t0001g0064others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+305_815+308del others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619797 | ||||||
chr5:6619810
|
A | G | 86 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(83): Show | 97 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.815+296T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619810 | ||||||
chr5:6619848
|
CTGTTT | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(23): Show | 34 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.815+253_815+257del others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619848 | ||||||
chr5:6619979
|
C | T | 86 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(83): Show | 97 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.815+127G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619979 | ||||||
chr5:6620034
|
A | G | 5 | a0001c0003t0001g0062a0001c0003t0001g0065a0002c0006t0001g0064others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+72T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6620034 | ||||||
chr5:6620080
|
G | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.815+26C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6620080 | ||||||
chr5:6620346
|
A | G | 250 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(247): Show | 287 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.623-48T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620346 | ||||||
chr5:6620546
|
G | T | 119 | a0001c0001t0001g0232a0001c0001t0001g0267a0001c0001t0001g0275others(116): Show | 137 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.623-248C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620546 | ||||||
chr5:6620597
|
C | CA | 10 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(7): Show | 10 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.623-300dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620597 | ||||||
chr5:6620731
|
C | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(23): Show | 34 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.623-433G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620731 | ||||||
chr5:6620816
|
A | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.623-518T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620816 | ||||||
chr5:6620874
|
T | G | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG00597.hp2 HG02135.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-576A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620874 | ||||||
chr5:6620918
|
A | G | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 284 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.623-620T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620918 | ||||||
chr5:6621046
|
C | G | 1 | a0001c0001t0001g0357 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.623-748G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621046 | ||||||
chr5:6621097
|
A | G | 252 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(249): Show | 289 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.623-799T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621097 | ||||||
chr5:6621105
|
A | C | 116 | a0001c0001t0001g0232a0001c0001t0001g0267a0001c0001t0001g0275others(113): Show | 133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.623-807T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621105 | ||||||
chr5:6621171
|
G | A | 2 | a0001c0002t0001g0283a0006c0020t0001g0282 | 2 | HG02683.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.622+845C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621171 | ||||||
chr5:6621224
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0333 | 2 | HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.622+792C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621224 | ||||||
chr5:6621304
|
T | C | 1 | a0001c0002t0001g0308 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.622+712A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621304 | ||||||
chr5:6621335
|
C | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(14): Show | 23 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.622+681G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621335 | ||||||
chr5:6621368
|
A | G | 3 | a0001c0004t0002g0167a0001c0004t0002g0201a0001c0004t0002g0202 | 3 | HG00140.hp2 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.622+648T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621368 | ||||||
chr5:6621476
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0163others(11): Show | 17 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.622+540A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621476 | ||||||
chr5:6621486
|
C | T | 2 | a0004c0008t0001g0367a0004c0008t0001g0368 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.622+530G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621486 | ||||||
chr5:6621487
|
A | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0163others(15): Show | 21 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.622+529T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621487 | ||||||
chr5:6621488
|
C | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0163others(8): Show | 14 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+528G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621488 | ||||||
chr5:6621515
|
A | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02818.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622+501T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621515 | ||||||
chr5:6621527
|
T | G | 1 | a0001c0003t0001g0112 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.622+489A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621527 | ||||||
chr5:6621533
|
G | A | 2 | a0002c0006t0003g0094a0002c0006t0003g0096 | 2 | HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.622+483C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621533 | ||||||
chr5:6621564
|
T | C | 5 | a0001c0002t0001g0284a0001c0003t0001g0019a0001c0003t0001g0088others(2): Show | 6 | NA18940.hp1 NA18942.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+452A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621564 | ||||||
chr5:6621576
|
G | A | 2 | a0001c0001t0004g0138a0001c0001t0004g0208 | 2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.622+440C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621576 | ||||||
chr5:6621597
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+419T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621597 | ||||||
chr5:6621606
|
G | A | 1 | a0004c0008t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.622+410C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621606 | ||||||
chr5:6621653
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.622+363G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621653 | ||||||
chr5:6621747
|
C | CA | 224 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(221): Show | 255 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.622+268dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621747 | ||||||
chr5:6621747
|
C | CAA | 16 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(13): Show | 22 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.622+267_622+268dup others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621747 | ||||||
chr5:6621904
|
T | G | 91 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(88): Show | 102 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.622+112A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621904 | ||||||
chr5:6622009
|
T | A | 1 | a0002c0007t0003g0006 | 4 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.622+7A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6622009 | ||||||
chr5:6622012
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.622+4T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6622012 | ||||||
chr5:6622103
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.538-3T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622103 | ||||||
chr5:6622106
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.538-6T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622106 | ||||||
chr5:6622107
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.538-7T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622107 | ||||||
chr5:6622109
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-9T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622109 | ||||||
chr5:6622114
|
A | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-14T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622114 | ||||||
chr5:6622116
|
G | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-16C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622116 | ||||||
chr5:6622124
|
T | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-24A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622124 | ||||||
chr5:6622127
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-27T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622127 | ||||||
chr5:6622129
|
G | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-29C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622129 | ||||||
chr5:6622134
|
T | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-34A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622134 | ||||||
chr5:6622142
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-42G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622142 | ||||||
chr5:6622145
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-45T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622145 | ||||||
chr5:6622147
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-47T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622147 | ||||||
chr5:6622150
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-50G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622150 | ||||||
chr5:6622152
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-52T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622152 | ||||||
chr5:6622156
|
T | A | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-56A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622156 | ||||||
chr5:6622158
|
A | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-58T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622158 | ||||||
chr5:6622159
|
A | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-59T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622159 | ||||||
chr5:6622163
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-63T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622163 | ||||||
chr5:6622164
|
A | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-64T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622164 | ||||||
chr5:6622165
|
A | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-65T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622165 | ||||||
chr5:6622166
|
G | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-66C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622166 | ||||||
chr5:6622169
|
A | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-69T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622169 | ||||||
chr5:6622172
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-72G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622172 | ||||||
chr5:6622174
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-74T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622174 | ||||||
chr5:6622175
|
G | GATGGGGT others(8): Show |
1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-76_538-75insAA others(13): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622175 | ||||||
chr5:6622187
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-87G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622187 | ||||||
chr5:6622192
|
C | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-92G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622192 | ||||||
chr5:6622201
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-101T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622201 | ||||||
chr5:6622202
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-102T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622202 | ||||||
chr5:6622208
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-108G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622208 | ||||||
chr5:6622209
|
T | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-109A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622209 | ||||||
chr5:6622210
|
T | C | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-110A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622210 | ||||||
chr5:6622215
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-115T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622215 | ||||||
chr5:6622222
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-122G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622222 | ||||||
chr5:6622223
|
T | A | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-123A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622223 | ||||||
chr5:6622224
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-124T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622224 | ||||||
chr5:6622229
|
A | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-129T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622229 | ||||||
chr5:6622233
|
C | G | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-133G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622233 | ||||||
chr5:6622233
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.538-133G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622233 | ||||||
chr5:6622235
|
T | A | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-135A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622235 | ||||||
chr5:6622241
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-141T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622241 | ||||||
chr5:6622243
|
TTTTAGGG others(12): Show |
T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-162_538-144del others(19): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622243 | ||||||
chr5:6622267
|
A | T | 1 | a0001c0004t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-167T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622267 | ||||||
chr5:6622469
|
T | C | 2 | a0001c0004t0002g0135a0001c0004t0002g0136 | 2 | NA18971.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.538-369A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622469 | ||||||
chr5:6622555
|
A | C | 1 | a0001c0001t0001g0232 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.538-455T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622555 | ||||||
chr5:6622589
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(3): Show | 7 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.538-489A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622589 | ||||||
chr5:6622622
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.538-522G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622622 | ||||||
chr5:6622676
|
C | T | 25 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0124others(22): Show | 32 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.537+538G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622676 | ||||||
chr5:6622677
|
G | A | 83 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(80): Show | 94 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.537+537C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622677 | ||||||
chr5:6622717
|
C | T | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+497G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622717 | ||||||
chr5:6622747
|
T | A | 1 | a0001c0003t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.537+467A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622747 | ||||||
chr5:6622790
|
T | C | 1 | a0001c0001t0001g0041 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.537+424A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622790 | ||||||
chr5:6622847
|
C | CA | 6 | a0001c0002t0001g0231a0001c0002t0001g0286a0001c0003t0001g0055others(3): Show | 6 | HG01074.hp2 HG01978.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+366dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622847 | ||||||
chr5:6622847
|
C | CAA | 208 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(205): Show | 237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.537+365_537+366dup others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622847 | ||||||
chr5:6622911
|
A | G | 1 | a0003c0005t0001g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.537+303T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622911 | ||||||
chr5:6622965
|
C | T | 1 | a0004c0008t0001g0367 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.537+249G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622965 | ||||||
chr5:6622972
|
T | C | 213 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0127others(210): Show | 242 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.537+242A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622972 | ||||||
chr5:6622975
|
G | A | 1 | a0003c0005t0001g0285 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.537+239C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622975 | ||||||
chr5:6623044
|
GA | G | 38 | a0001c0001t0001g0029a0001c0001t0001g0124a0001c0001t0001g0125others(35): Show | 46 | HG00642.hp2 HG00738.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.537+169delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623044 | ||||||
chr5:6623044
|
GAA | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+168_537+169del others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623044 | ||||||
chr5:6623074
|
G | A | 4 | a0001c0013t0001g0213a0001c0013t0001g0214a0001c0013t0001g0215others(1): Show | 4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+140C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623074 | ||||||
chr5:6623097
|
G | C | 1 | a0001c0010t0002g0119 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.537+117C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623097 | ||||||
chr5:6623110
|
A | T | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+104T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623110 | ||||||
chr5:6623137
|
A | G | 4 | a0001c0010t0001g0057a0001c0010t0001g0058a0001c0010t0001g0059others(1): Show | 4 | HG01256.hp1 HG01257.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+77T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623137 | ||||||
chr5:6623205
|
A | G | 6 | a0001c0004t0001g0008a0001c0004t0001g0154a0001c0004t0001g0155others(3): Show | 8 | HG02257.hp2 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+9T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623205 | ||||||
chr5:6623206
|
T | C | 1 | a0002c0006t0003g0095 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.537+8A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623206 | ||||||
chr5:6623319
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-34C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623319 | ||||||
chr5:6623319
|
G | GA | 309 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0041others(306): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.466-35dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623319 | ||||||
chr5:6623319
|
G | GAA | 25 | a0001c0001t0001g0289a0001c0001t0001g0331a0001c0001t0001g0332others(22): Show | 25 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.466-36_466-35dupTT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623319 | ||||||
chr5:6623334
|
C | T | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-49G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623334 | ||||||
chr5:6623585
|
G | C | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-300C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623585 | ||||||
chr5:6623855
|
CCT | C | 92 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(89): Show | 103 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.466-572_466-571del others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623855 | ||||||
chr5:6623955
|
C | G | 3 | a0001c0004t0002g0023a0001c0004t0002g0148a0001c0004t0002g0149 | 4 | HG02040.hp2 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-670G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623955 | ||||||
chr5:6624181
|
C | A | 92 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(89): Show | 103 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.466-896G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624181 | ||||||
chr5:6624258
|
C | T | 83 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(80): Show | 94 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.466-973G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624258 | ||||||
chr5:6624282
|
G | A | 121 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0232others(118): Show | 139 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.466-997C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624282 | ||||||
chr5:6624406
|
A | G | 1 | a0001c0003t0001g0099 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.466-1121T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624406 | ||||||
chr5:6624482
|
C | T | 5 | a0001c0003t0001g0062a0001c0003t0001g0063a0001c0003t0001g0065others(2): Show | 5 | HG02572.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1082G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624482 | ||||||
chr5:6624787
|
G | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+777C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624787 | ||||||
chr5:6624808
|
TTAGAAAA | T | 92 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0001g0146others(89): Show | 103 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.465+749_465+755del others(7): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624808 | ||||||
chr5:6624861
|
C | A | 120 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0232others(117): Show | 138 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.465+703G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624861 | ||||||
chr5:6625018
|
T | C | 1 | a0001c0002t0001g0290 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.465+546A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625018 | ||||||
chr5:6625078
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.465+486C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625078 | ||||||
chr5:6625102
|
G | GAA | 14 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0130others(11): Show | 19 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.465+460_465+461dup others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625102 | ||||||
chr5:6625478
|
G | A | 2 | a0001c0002t0001g0291a0001c0002t0001g0292 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.465+86C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625478 | ||||||
chr5:6625844
|
A | C | 1 | a0001c0001t0001g0334 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.360-175T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6625844 | ||||||
chr5:6625935
|
T | G | 5 | a0001c0002t0001g0035a0001c0002t0001g0217a0001c0002t0001g0293others(2): Show | 6 | NA18988.hp1 NA18989.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.360-266A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6625935 | ||||||
chr5:6625978
|
G | A | 63 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(60): Show | 72 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.360-309C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6625978 | ||||||
chr5:6626060
|
C | T | 1 | a0001c0004t0002g0147 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.360-391G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626060 | ||||||
chr5:6626117
|
A | G | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-448T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626117 | ||||||
chr5:6626125
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.360-456A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626125 | ||||||
chr5:6626133
|
T | C | 4 | a0001c0002t0001g0040a0001c0002t0001g0315a0001c0002t0001g0316others(1): Show | 5 | HG00609.hp1 NA18991.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-464A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626133 | ||||||
chr5:6626325
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.360-656A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626325 | ||||||
chr5:6626380
|
CT | C | 103 | a0001c0001t0001g0232a0001c0001t0001g0267a0001c0001t0001g0275others(100): Show | 118 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.360-712delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626380 | ||||||
chr5:6626424
|
T | C | 1 | a0002c0007t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.360-755A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626424 | ||||||
chr5:6626448
|
T | C | 247 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(244): Show | 283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.360-779A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626448 | ||||||
chr5:6626560
|
C | G | 251 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(248): Show | 287 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.360-891G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626560 | ||||||
chr5:6626595
|
C | A | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-926G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626595 | ||||||
chr5:6626697
|
G | A | 1 | a0001c0004t0002g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.360-1028C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626697 | ||||||
chr5:6626884
|
T | C | 1 | a0001c0003t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.360-1215A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626884 | ||||||
chr5:6626945
|
A | C | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1276T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626945 | ||||||
chr5:6627087
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(3): Show | 7 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.360-1418G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627087 | ||||||
chr5:6627299
|
T | C | 6 | a0001c0003t0001g0007a0001c0003t0001g0116a0001c0003t0001g0117others(3): Show | 8 | HG01943.hp2 HG01993.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-1630A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627299 | ||||||
chr5:6627376
|
A | T | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360-1707T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627376 | ||||||
chr5:6627542
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-1873C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627542 | ||||||
chr5:6627761
|
T | A | 1 | a0001c0003t0001g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.360-2092A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627761 | ||||||
chr5:6627866
|
A | G | 3 | a0001c0002t0001g0031a0001c0002t0001g0218a0001c0002t0001g0224 | 4 | HG02155.hp2 NA18971.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-2197T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627866 | ||||||
chr5:6627884
|
C | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0004g0323 | 3 | HG01255.hp2 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.360-2215G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627884 | ||||||
chr5:6627997
|
G | A | 3 | a0002c0006t0003g0094a0002c0006t0003g0095a0002c0006t0003g0096 | 3 | HG01106.hp1 HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.360-2328C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627997 | ||||||
chr5:6628068
|
C | T | 9 | a0001c0009t0001g0047a0001c0009t0001g0048a0001c0009t0001g0049others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360-2399G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628068 | ||||||
chr5:6628085
|
T | C | 15 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(12): Show | 20 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-2416A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628085 | ||||||
chr5:6628351
|
A | T | 126 | a0001c0001t0001g0029a0001c0001t0001g0126a0001c0001t0001g0127others(123): Show | 145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.360-2682T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628351 | ||||||
chr5:6628414
|
A | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0219a0001c0001t0001g0220others(3): Show | 7 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.360-2745T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628414 | ||||||
chr5:6628419
|
A | T | 1 | a0001c0003t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.360-2750T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628419 | ||||||
chr5:6628522
|
T | A | 1 | a0001c0002t0001g0297 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.360-2853A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628522 | ||||||
chr5:6628928
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.359+2945G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628928 | ||||||
chr5:6628929
|
G | A | 2 | a0001c0013t0001g0215a0001c0013t0001g0216 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.359+2944C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628929 | ||||||
chr5:6629368
|
C | G | 1 | a0001c0004t0002g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+2505G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629368 | ||||||
chr5:6629500
|
T | A | 1 | a0001c0003t0001g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.359+2373A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629500 | ||||||
chr5:6629721
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+2152C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629721 | ||||||
chr5:6629756
|
C | A | 1 | a0001c0003t0001g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359+2117G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629756 | ||||||
chr5:6629817
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(113): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.359+2056C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629817 | ||||||
chr5:6629925
|
C | T | 4 | a0001c0013t0001g0213a0001c0013t0001g0214a0001c0013t0001g0215others(1): Show | 4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+1948G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629925 | ||||||
chr5:6629990
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.359+1883T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629990 | ||||||
chr5:6630005
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.359+1868A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630005 | ||||||
chr5:6630161
|
A | G | 1 | a0001c0002t0001g0223 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.359+1712T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630161 | ||||||
chr5:6630435
|
G | C | 2 | a0001c0002t0001g0036a0001c0002t0001g0298 | 3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.359+1438C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630435 | ||||||
chr5:6630496
|
G | C | 2 | a0001c0002t0001g0365a0001c0002t0001g0366 | 2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.359+1377C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630496 | ||||||
chr5:6630826
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0004g0208 | 3 | HG02572.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.359+1047C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630826 | ||||||
chr5:6630870
|
G | A | 3 | a0001c0004t0002g0209a0001c0004t0002g0210a0001c0004t0002g0211 | 3 | HG02602.hp2 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.359+1003C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630870 | ||||||
chr5:6630880
|
G | A | 115 | a0001c0001t0001g0232a0001c0001t0001g0267a0001c0001t0001g0275others(112): Show | 132 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.359+993C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630880 | ||||||
chr5:6630913
|
A | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0141others(87): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.359+960T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630913 | ||||||
chr5:6631222
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.359+651G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631222 | ||||||
chr5:6631229
|
G | A | 1 | a0001c0001t0001g0360 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.359+644C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631229 | ||||||
chr5:6631282
|
TACA | T | 4 | a0001c0010t0001g0057a0001c0010t0001g0058a0001c0010t0001g0059others(1): Show | 4 | HG01256.hp1 HG01257.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.359+588_359+590del others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631282 | ||||||
chr5:6631377
|
C | A | 10 | a0001c0003t0001g0055a0001c0009t0001g0047a0001c0009t0001g0048others(7): Show | 11 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.359+496G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631377 | ||||||
chr5:6631394
|
T | C | 1 | a0001c0001t0001g0361 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.359+479A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631394 | ||||||
chr5:6631527
|
G | A | 26 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0039others(23): Show | 30 | HG00609.hp1 HG02074.hp1 HG02523.hp1 others(27): Show |
intron_variant | MODIFIER | c.359+346C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631527 | ||||||
chr5:6631653
|
C | G | 1 | a0001c0013t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359+220G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631653 | ||||||
chr5:6631692
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.359+181T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631692 | ||||||
chr5:6631823
|
G | C | 10 | a0001c0003t0001g0055a0001c0009t0001g0047a0001c0009t0001g0048others(7): Show | 11 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.359+50C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631823 | ||||||
chr5:6632011
|
A | G | 1 | a0001c0003t0001g0056 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.255-34T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632011 | ||||||
chr5:6632030
|
T | C | 2 | a0001c0003t0001g0120a0001c0003t0001g0121 | 2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.255-53A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632030 | ||||||
chr5:6632052
|
C | T | 4 | a0001c0013t0001g0213a0001c0013t0001g0214a0001c0013t0001g0215others(1): Show | 4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-75G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632052 | ||||||
chr5:6632182
|
T | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0141others(87): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.255-205A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632182 | ||||||
chr5:6632207
|
C | A | 246 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(243): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.255-230G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632207 | ||||||
chr5:6632211
|
A | AT | 246 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(243): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.255-235_255-234ins others(1): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632211 | ||||||
chr5:6632228
|
CA | C | 3 | a0001c0011t0001g0013a0001c0011t0001g0045a0001c0011t0001g0046 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-252delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632228 | ||||||
chr5:6632254
|
T | C | 1 | a0001c0002t0001g0363 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.255-277A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632254 | ||||||
chr5:6632316
|
T | C | 2 | a0001c0003t0001g0022a0001c0003t0001g0122 | 3 | HG02615.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.254+283A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632316 | ||||||
chr5:6632500
|
G | A | 3 | a0001c0002t0001g0364a0001c0002t0001g0365a0001c0002t0001g0366 | 3 | HG00673.hp1 HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.254+99C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632500 | ||||||
chr5:6632762
|
G | A | 88 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(85): Show | 99 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(96): Show |
splice_region_variant&intron_variant | LOW | c.97-6C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632762 | ||||||
chr5:6632796
|
G | A | 199 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0124others(196): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.97-40C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632796 | ||||||
chr5:6632829
|
G | T | 199 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0124others(196): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.96+55C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632829 | ||||||
chr5:6632832
|
C | A | 1 | a0001c0003t0001g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+52G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632832 | ||||||
chr5:6632867
|
C | T | 2 | a0004c0008t0001g0367a0004c0008t0001g0368 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.96+17G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632867 |