geneid | 79730 |
---|---|
ensemblid | ENSG00000179299.17 |
hgncid | 25857 |
symbol | NSUN7 |
name | NOP2/Sun RNA methyltransferase family member 7 |
refseq_nuc | NM_024677.6 |
refseq_prot | NP_078953.4 |
ensembl_nuc | ENST00000381782.7 |
ensembl_prot | ENSP00000371201.2 |
mane_status | MANE Select |
chr | chr4 |
start | 40749955 |
end | 40811184 |
strand | + |
ver | v1.2 |
region | chr4:40749955-40811184 |
region5000 | chr4:40744955-40816184 |
regionname0 | NSUN7_chr4_40749955_40811184 |
regionname5000 | NSUN7_chr4_40744955_40816184 |
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 | 0/1 | 718 | 212 | 48 | 45 | 96 | 6 | 16 | 80 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002 | 0/0 | 718 | 100 | 12 | 5 | 67 | 0 | 16 | 53 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003 | 0/0 | 718 | 50 | 13 | 24 | 6 | 2 | 5 | 5 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0004 | 0/0 | 718 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0005 | 0/0 | 718 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0006 | 0/0 | 718 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0007 | 1/0 | 718 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0008 | 0/0 | 718 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0009 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0010 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0011 | 0/0 | 218 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0012 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0013 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0014 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0015 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0016 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0017 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0018 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0019 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
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 | 0/1 | 2157 | 211 | 47 | 45 | 96 | 6 | 16 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0002 | 0/0 | 2157 | 99 | 12 | 4 | 67 | 0 | 16 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0003 | 0/0 | 2157 | 49 | 13 | 24 | 6 | 2 | 4 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0004 | 0/0 | 2157 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0005 | 1/0 | 2157 | 3 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0006 | 0/0 | 2157 | 3 | 2 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0007 | 0/0 | 2157 | 3 | 1 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0008 | 0/0 | 2157 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0009 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0010 | 0/0 | 2157 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0011 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0012 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0013 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0014 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0015 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0016 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0017 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0018 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0019 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0020 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0021 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0022 | 0/0 | 2157 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
c0023 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
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 | 2683 | 194 | 29 | 27 | 116 | 1 | 19 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0002 | 0/0 | 2682 | 50 | 11 | 11 | 23 | 3 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0003 | 0/0 | 2687 | 27 | 1 | 17 | 1 | 2 | 6 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0004 | 0/0 | 2684 | 21 | 2 | 3 | 13 | 0 | 3 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0005 | 0/0 | 2684 | 12 | 0 | 3 | 7 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0006 | 0/0 | 2688 | 8 | 2 | 4 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0007 | 0/0 | 2684 | 7 | 2 | 0 | 5 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0008 | 0/0 | 2685 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0009 | 0/0 | 2686 | 6 | 1 | 3 | 0 | 2 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0010 | 0/0 | 2681 | 6 | 6 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0011 | 0/0 | 2684 | 4 | 3 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0012 | 0/0 | 2685 | 3 | 2 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0013 | 0/0 | 2683 | 3 | 0 | 1 | 0 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0014 | 0/0 | 2685 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0015 | 0/0 | 2685 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0016 | 0/0 | 2685 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0017 | 0/0 | 2687 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0018 | 0/0 | 2682 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0019 | 0/0 | 2682 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0020 | 0/0 | 2686 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0021 | 0/0 | 2689 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0022 | 0/0 | 2688 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0023 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0024 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0025 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0026 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0027 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0028 | 0/0 | 2684 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0029 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0030 | 0/0 | 2689 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0031 | 0/0 | 2687 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0032 | 0/0 | 2686 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0033 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0034 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0035 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0036 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0037 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0038 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0039 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0040 | 0/0 | 2686 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0041 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0042 | 0/0 | 2683 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0043 | 0/0 | 2682 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0044 | 0/0 | 2684 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0045 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0046 | 0/0 | 2686 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0047 | 0/0 | 2687 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
t0048 | 0/0 | 2689 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0003 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
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 | 0/1 | 2157 | 211 | 47 | 45 | 96 | 6 | 16 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0013 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002 | 0/0 | 2157 | 99 | 12 | 4 | 67 | 0 | 16 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0010 | 0/0 | 2157 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003 | 0/0 | 2157 | 49 | 13 | 24 | 6 | 2 | 4 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0022 | 0/0 | 2157 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0004c0004 | 0/0 | 2157 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0004c0014 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0005c0007 | 0/0 | 2157 | 3 | 1 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0006c0006 | 0/0 | 2157 | 3 | 2 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0007c0005 | 1/0 | 2157 | 3 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0008c0008 | 0/0 | 2157 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0009c0023 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0010c0021 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0011c0019 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0012c0015 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0013c0012 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0014c0016 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0015c0017 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0016c0011 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0017c0018 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0018c0020 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0019c0009 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4839 | 116 | 25 | 22 | 61 | 1 | 6 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0002 | 0/0 | 4838 | 41 | 6 | 11 | 19 | 3 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0004 | 0/0 | 4840 | 10 | 2 | 3 | 4 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0005 | 0/0 | 4840 | 5 | 0 | 2 | 2 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0007 | 0/0 | 4840 | 6 | 1 | 0 | 5 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0009 | 0/0 | 4842 | 6 | 1 | 3 | 0 | 2 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0010 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0012 | 0/0 | 4841 | 3 | 2 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0013 | 0/0 | 4839 | 3 | 0 | 1 | 0 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0014 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0017 | 0/0 | 4843 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0018 | 0/0 | 4838 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0019 | 0/0 | 4838 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0020 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0027 | 0/0 | 4841 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0029 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0033 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0036 | 0/0 | 4838 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0037 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0038 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0039 | 0/0 | 4838 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0041 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0042 | 0/0 | 4839 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0043 | 0/0 | 4838 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0045 | 0/0 | 4844 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0001t0047 | 0/0 | 4843 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0001c0013t0002 | 0/0 | 4838 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0001 | 0/0 | 4839 | 69 | 2 | 2 | 52 | 0 | 13 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0002 | 0/0 | 4838 | 5 | 4 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0004 | 0/0 | 4840 | 10 | 0 | 0 | 8 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0005 | 0/0 | 4840 | 6 | 0 | 1 | 4 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0010 | 0/0 | 4837 | 5 | 5 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0014 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0024 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0026 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0002t0035 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0002c0010t0001 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0003 | 0/0 | 4843 | 25 | 1 | 17 | 1 | 2 | 4 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0006 | 0/0 | 4844 | 8 | 2 | 4 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0011 | 0/0 | 4840 | 4 | 3 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0014 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0015 | 0/0 | 4841 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0016 | 0/0 | 4841 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0021 | 0/0 | 4845 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0022 | 0/0 | 4844 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0025 | 0/0 | 4841 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0031 | 0/0 | 4843 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0032 | 0/0 | 4842 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0003t0044 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0003c0022t0003 | 0/0 | 4843 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0004c0004t0008 | 0/0 | 4841 | 6 | 6 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0004c0004t0046 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0004c0014t0008 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0005c0007t0028 | 0/0 | 4840 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0005c0007t0030 | 0/0 | 4845 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0005c0007t0048 | 0/0 | 4845 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0006c0006t0003 | 0/0 | 4843 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0006c0006t0015 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0006c0006t0034 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0007c0005t0001 | 1/0 | 4839 | 3 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0008c0008t0001 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0008c0008t0005 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0009c0023t0001 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0010c0021t0002 | 0/0 | 4838 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0011c0019t0002 | 0/0 | 4828 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0012c0015t0040 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0013c0012t0001 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0014c0016t0002 | 0/0 | 4838 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0015c0017t0023 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0016c0011t0004 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0017c0018t0001 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0018c0020t0001 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
a0019c0009t0007 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | copy fasta | chr4 | 40744955 | 40816184 |
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 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0009g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0009g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0009g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0009g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0009g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0012g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0012g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0013g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0013g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0013g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0017g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0017g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0018g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0018g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0019g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0020g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0027g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0029g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0033g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0036g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0037g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0038g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0039g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0041g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0042g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0043g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0045g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0001t0047g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0001c0013t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0014g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0024g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0026g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0002t0035g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0002c0010t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0006g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0011g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0014g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0016g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0016g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0016g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0021g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0022g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0025g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0032g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0003t0044g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0003c0022t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0004t0046g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0004c0014t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0005c0007t0028g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0005c0007t0030g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0005c0007t0048g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0006c0006t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0006c0006t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0006c0006t0034g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0007c0005t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0007c0005t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0007c0005t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0008c0008t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0008c0008t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0009c0023t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0010c0021t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0011c0019t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0012c0015t0040g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0013c0012t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0014c0016t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0015c0017t0023g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0016c0011t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0017c0018t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0018c0020t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
a0019c0009t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0003 | g0226 | EUR | GBR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | GBR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00423 | hp2 | a0002 | c0002 | t0004 | g0295 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00438 | hp1 | a0003 | c0003 | t0022 | g0042 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00438 | hp2 | a0002 | c0002 | t0005 | g0289 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00597 | hp2 | a0015 | c0017 | t0023 | g0118 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00639 | hp2 | a0007 | c0005 | t0001 | g0282 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00642 | hp2 | a0003 | c0003 | t0006 | g0049 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00733 | hp2 | a0003 | c0003 | t0003 | g0030 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0034 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0339 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG00738 | hp2 | a0003 | c0003 | t0003 | g0228 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01069 | hp1 | a0003 | c0003 | t0003 | g0033 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01069 | hp2 | a0003 | c0003 | t0006 | g0060 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01071 | hp1 | a0003 | c0003 | t0003 | g0032 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01074 | hp1 | a0003 | c0003 | t0003 | g0263 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0349 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01081 | hp1 | a0003 | c0003 | t0003 | g0040 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01081 | hp2 | a0003 | c0003 | t0003 | g0351 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01099 | hp1 | a0003 | c0003 | t0003 | g0044 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0036 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01109 | hp2 | a0003 | c0003 | t0006 | g0059 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01167 | hp2 | a0003 | c0003 | t0025 | g0161 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01168 | hp2 | a0003 | c0003 | t0003 | g0028 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01169 | hp2 | a0003 | c0003 | t0011 | g0162 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01175 | hp2 | a0003 | c0003 | t0003 | g0350 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01192 | hp1 | a0001 | c0001 | t0036 | g0215 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01192 | hp2 | a0001 | c0001 | t0017 | g0180 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01243 | hp1 | a0005 | c0007 | t0028 | g0043 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01243 | hp2 | a0007 | c0005 | t0001 | g0294 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01255 | hp1 | a0003 | c0003 | t0003 | g0352 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01255 | hp2 | a0003 | c0003 | t0003 | g0237 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0115 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01258 | hp1 | a0002 | c0010 | t0001 | g0051 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01261 | hp2 | a0003 | c0003 | t0003 | g0231 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01358 | hp1 | a0005 | c0007 | t0048 | g0236 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01361 | hp1 | a0003 | c0003 | t0032 | g0039 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01361 | hp2 | a0001 | c0001 | t0013 | g0341 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01496 | hp2 | a0003 | c0003 | t0003 | g0347 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01516 | hp2 | a0001 | c0001 | t0009 | g0336 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01517 | hp1 | a0001 | c0001 | t0009 | g0335 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01517 | hp2 | a0003 | c0003 | t0003 | g0029 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01891 | hp1 | a0002 | c0002 | t0024 | g0171 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01928 | hp2 | a0001 | c0001 | t0038 | g0178 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01975 | hp1 | a0002 | c0002 | t0026 | g0065 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01978 | hp1 | a0002 | c0002 | t0005 | g0311 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01981 | hp1 | a0003 | c0003 | t0003 | g0035 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0338 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0343 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02055 | hp2 | a0005 | c0007 | t0030 | g0045 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02071 | hp2 | a0017 | c0018 | t0001 | g0364 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02080 | hp2 | a0010 | c0021 | t0002 | g0083 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02129 | hp2 | a0009 | c0023 | t0001 | g0027 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02145 | hp1 | a0001 | c0001 | t0020 | g0331 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02258 | hp1 | a0001 | c0001 | t0019 | g0224 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02280 | hp1 | a0019 | c0009 | t0007 | g0332 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02280 | hp2 | a0004 | c0004 | t0046 | g0067 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02300 | hp1 | a0003 | c0003 | t0006 | g0061 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02523 | hp1 | a0008 | c0008 | t0001 | g0062 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02602 | hp1 | a0002 | c0002 | t0005 | g0296 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02602 | hp2 | a0001 | c0001 | t0042 | g0232 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02622 | hp1 | a0001 | c0001 | t0045 | g0066 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02630 | hp2 | a0004 | c0004 | t0008 | g0072 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0212 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02698 | hp2 | a0001 | c0001 | t0043 | g0091 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02717 | hp2 | a0002 | c0002 | t0010 | g0135 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02723 | hp2 | a0001 | c0001 | t0037 | g0156 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02809 | hp2 | a0001 | c0001 | t0019 | g0223 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02818 | hp1 | a0003 | c0003 | t0011 | g0163 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02895 | hp2 | a0002 | c0002 | t0010 | g0096 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02922 | hp2 | a0003 | c0003 | t0044 | g0160 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02965 | hp1 | a0003 | c0003 | t0016 | g0355 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02965 | hp2 | a0004 | c0004 | t0008 | g0069 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02970 | hp2 | a0001 | c0013 | t0002 | g0153 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02976 | hp1 | a0004 | c0004 | t0008 | g0068 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02976 | hp2 | a0001 | c0001 | t0039 | g0230 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0175 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03041 | hp2 | a0003 | c0003 | t0015 | g0240 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03098 | hp2 | a0004 | c0004 | t0008 | g0071 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03130 | hp1 | a0013 | c0012 | t0001 | g0011 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03130 | hp2 | a0004 | c0004 | t0008 | g0070 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03139 | hp1 | a0004 | c0004 | t0008 | g0073 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03139 | hp2 | a0001 | c0001 | t0033 | g0081 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03195 | hp2 | a0004 | c0014 | t0008 | g0046 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03209 | hp1 | a0012 | c0015 | t0040 | g0174 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0313 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03239 | hp1 | a0003 | c0003 | t0003 | g0038 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03239 | hp2 | a0003 | c0003 | t0003 | g0340 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03453 | hp1 | a0003 | c0003 | t0011 | g0159 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03453 | hp2 | a0002 | c0002 | t0010 | g0166 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03486 | hp1 | a0003 | c0003 | t0016 | g0361 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03491 | hp1 | a0003 | c0003 | t0003 | g0348 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03491 | hp2 | a0002 | c0002 | t0004 | g0018 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03492 | hp2 | a0002 | c0002 | t0004 | g0018 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03516 | hp1 | a0003 | c0003 | t0031 | g0031 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03516 | hp2 | a0003 | c0003 | t0011 | g0177 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03579 | hp1 | a0003 | c0003 | t0015 | g0158 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03579 | hp2 | a0001 | c0001 | t0047 | g0074 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0304 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03654 | hp2 | a0003 | c0022 | t0003 | g0353 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0052 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0305 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03704 | hp1 | a0001 | c0001 | t0013 | g0346 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0303 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0328 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0274 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03831 | hp2 | a0001 | c0001 | t0012 | g0344 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03834 | hp2 | a0001 | c0001 | t0027 | g0342 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04115 | hp1 | a0006 | c0006 | t0003 | g0309 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0299 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04199 | hp1 | a0001 | c0001 | t0013 | g0334 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0284 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0330 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18906 | hp1 | a0006 | c0006 | t0034 | g0363 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18947 | hp1 | a0002 | c0002 | t0005 | g0323 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18947 | hp2 | a0003 | c0003 | t0021 | g0037 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18948 | hp2 | a0011 | c0019 | t0002 | g0104 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18956 | hp2 | a0002 | c0002 | t0004 | g0308 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18965 | hp2 | a0002 | c0002 | t0004 | g0325 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18967 | hp2 | a0002 | c0002 | t0004 | g0273 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18969 | hp2 | a0001 | c0001 | t0007 | g0242 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18970 | hp1 | a0003 | c0003 | t0006 | g0369 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18973 | hp2 | a0003 | c0003 | t0006 | g0368 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18979 | hp1 | a0002 | c0002 | t0004 | g0333 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18983 | hp2 | a0001 | c0001 | t0018 | g0023 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18984 | hp2 | a0016 | c0011 | t0004 | g0366 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18985 | hp2 | a0001 | c0001 | t0041 | g0248 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18987 | hp2 | a0002 | c0002 | t0004 | g0329 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18989 | hp1 | a0002 | c0002 | t0005 | g0365 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18990 | hp2 | a0001 | c0001 | t0029 | g0250 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18995 | hp2 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18999 | hp2 | a0003 | c0003 | t0014 | g0167 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19003 | hp2 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0246 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19004 | hp2 | a0002 | c0002 | t0004 | g0261 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19056 | hp1 | a0002 | c0002 | t0004 | g0276 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19056 | hp2 | a0014 | c0016 | t0002 | g0185 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0367 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19067 | hp2 | a0002 | c0002 | t0005 | g0170 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19077 | hp1 | a0001 | c0001 | t0014 | g0131 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19077 | hp2 | a0002 | c0002 | t0014 | g0314 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19079 | hp1 | a0002 | c0002 | t0035 | g0357 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19079 | hp2 | a0008 | c0008 | t0005 | g0020 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0359 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19090 | hp2 | a0001 | c0001 | t0018 | g0024 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0243 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0362 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20129 | hp1 | a0003 | c0003 | t0003 | g0217 | AFR | ASW | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0290 | AFR | ASW | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0210 | EUR | TSI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0281 | SAS | GIH | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0280 | SAS | GIH | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01123 | hp1 | a0001 | c0001 | t0009 | g0345 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0312 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02486 | hp1 | a0002 | c0002 | t0010 | g0119 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02559 | hp1 | a0006 | c0006 | t0015 | g0168 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG02559 | hp2 | a0003 | c0003 | t0006 | g0165 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03471 | hp1 | a0003 | c0003 | t0006 | g0370 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
HG06807 | hp2 | a0003 | c0003 | t0016 | g0239 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20300 | hp1 | a0002 | c0002 | t0010 | g0144 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA20300 | hp2 | a0001 | c0001 | t0010 | g0225 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | LWK | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
NA21309 | hp2 | a0018 | c0020 | t0001 | g0319 | AFR | LWK | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
homoSapiens_grch38 | hp1 | a0007 | c0005 | t0001 | g0003 | REF | REF | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:40750709
|
G | T | 1 | a0009 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.16G>T | p.Gly6Cys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 453/4839 | 16/2157 | 6/718 | chr4 | 40750709 | ||
chr4:40750718
|
G | A | 1 | a0019 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.25G>A | p.Glu9Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 462/4839 | 25/2157 | 9/718 | chr4 | 40750718 | ||
chr4:40761226
|
A | T | 1 | a0010 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.413A>T | p.Lys138Ile | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/12 | 850/4839 | 413/2157 | 138/718 | chr4 | 40761226 | ||
chr4:40774312
|
A | G | 1 | a0018 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.536A>G | p.His179Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/12 | 973/4839 | 536/2157 | 179/718 | chr4 | 40774312 | ||
chr4:40774777
|
GTTTATAA others(3): Show |
G | 1 | a0011 | 1 | NA18948.hp2 | frameshift_variant | HIGH | c.656_665delATAATAAT others(2): Show |
p.Tyr219fs | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/12 | 1093/4839 | 656/2157 | 219/718 | INFO_REALIGN_3_PRIME | chr4 | 40774777 | |
chr4:40776086
|
C | T | 1 | a0017 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.863C>T | p.Ala288Val | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1300/4839 | 863/2157 | 288/718 | chr4 | 40776086 | ||
chr4:40776145
|
T | G | 13 | a0001a0003a0004others(10): Show | 283 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
missense_variant | MODERATE | c.922T>G | p.Ser308Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1359/4839 | 922/2157 | 308/718 | chr4 | 40776145 | ||
chr4:40776239
|
T | C | 1 | a0008 | 2 | HG02523.hp1 NA19079.hp2 |
missense_variant | MODERATE | c.1016T>C | p.Phe339Ser | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1453/4839 | 1016/2157 | 339/718 | chr4 | 40776239 | ||
chr4:40790689
|
G | A | 1 | a0005 | 3 | HG01243.hp1 HG01358.hp1 HG02055.hp2 |
missense_variant | MODERATE | c.1124G>A | p.Arg375His | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/12 | 1561/4839 | 1124/2157 | 375/718 | chr4 | 40790689 | ||
chr4:40794465
|
A | G | 1 | a0015 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1271A>G | p.His424Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/12 | 1708/4839 | 1271/2157 | 424/718 | chr4 | 40794465 | ||
chr4:40808334
|
A | T | 1 | a0014 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.1552A>T | p.Asn518Tyr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1989/4839 | 1552/2157 | 518/718 | chr4 | 40808334 | ||
chr4:40808355
|
G | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1573G>A | p.Ala525Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2010/4839 | 1573/2157 | 525/718 | chr4 | 40808355 | ||
chr4:40808358
|
GCCAAGGG others(6): Show |
G | 1 | a0013 | 1 | HG03130.hp1 | frameshift_variant | HIGH | c.1577_1589delCCAAGG others(7): Show |
p.Ala526fs | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2014/4839 | 1577/2157 | 526/718 | chr4 | 40808358 | ||
chr4:40808375
|
T | G | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1593T>G | p.Asp531Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2030/4839 | 1593/2157 | 531/718 | chr4 | 40808375 | ||
chr4:40808376
|
G | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1594G>A | p.Gly532Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2031/4839 | 1594/2157 | 532/718 | chr4 | 40808376 | ||
chr4:40808382
|
G | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1600G>A | p.Glu534Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2037/4839 | 1600/2157 | 534/718 | chr4 | 40808382 | ||
chr4:40808385
|
T | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1603T>A | p.Leu535Met | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2040/4839 | 1603/2157 | 535/718 | chr4 | 40808385 | ||
chr4:40808386
|
T | A | 1 | a0013 | 1 | HG03130.hp1 | stop_gained | HIGH | c.1604T>A | p.Leu535* | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2041/4839 | 1604/2157 | 535/718 | chr4 | 40808386 | ||
chr4:40808388
|
G | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1606G>A | p.Gly536Ser | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2043/4839 | 1606/2157 | 536/718 | chr4 | 40808388 | ||
chr4:40808389
|
G | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1607G>A | p.Gly536Asp | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2044/4839 | 1607/2157 | 536/718 | chr4 | 40808389 | ||
chr4:40808394
|
T | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1612T>A | p.Ser538Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2049/4839 | 1612/2157 | 538/718 | chr4 | 40808394 | ||
chr4:40808395
|
C | A | 1 | a0013 | 1 | HG03130.hp1 | stop_gained | HIGH | c.1613C>A | p.Ser538* | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2050/4839 | 1613/2157 | 538/718 | chr4 | 40808395 | ||
chr4:40808397
|
T | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1615T>A | p.Ser539Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2052/4839 | 1615/2157 | 539/718 | chr4 | 40808397 | ||
chr4:40808398
|
C | A | 1 | a0013 | 1 | HG03130.hp1 | stop_gained | HIGH | c.1616C>A | p.Ser539* | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2053/4839 | 1616/2157 | 539/718 | chr4 | 40808398 | ||
chr4:40808406
|
G | A | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1624G>A | p.Glu542Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2061/4839 | 1624/2157 | 542/718 | chr4 | 40808406 | ||
chr4:40808418
|
A | AAATCAGT others(8): Show |
1 | a0013 | 1 | HG03130.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.1638_1639insTCAGTG others(9): Show |
p.Lys546_Lys547insSe others(13): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2076/4839 | 1639/2157 | 547/718 | INFO_REALIGN_3_PRIME | chr4 | 40808418 | |
chr4:40808472
|
A | C | 1 | a0012 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1690A>C | p.Met564Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2127/4839 | 1690/2157 | 564/718 | chr4 | 40808472 | ||
chr4:40808646
|
A | G | 3 | a0003a0005a0006 | 56 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(53): Show |
missense_variant | MODERATE | c.1864A>G | p.Thr622Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2301/4839 | 1864/2157 | 622/718 | chr4 | 40808646 | ||
chr4:40808730
|
A | G | 18 | a0001a0002a0003others(15): Show | 389 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(386): Show |
missense_variant | MODERATE | c.1948A>G | p.Lys650Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2385/4839 | 1948/2157 | 650/718 | chr4 | 40808730 | ||
chr4:40808839
|
T | G | 1 | a0004 | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.2057T>G | p.Val686Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2494/4839 | 2057/2157 | 686/718 | chr4 | 40808839 | ||
chr4:40808887
|
C | T | 1 | a0016 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.2105C>T | p.Pro702Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2542/4839 | 2105/2157 | 702/718 | chr4 | 40808887 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:40750813
|
G | C | 1 | a0002c0010 | 1 | HG01258.hp1 | synonymous_variant | LOW | c.120G>C | p.Thr40Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 557/4839 | 120/2157 | 40/718 | chr4 | 40750813 | ||
chr4:40750924
|
C | G | 1 | a0003c0022 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.231C>G | p.Ser77Ser | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 668/4839 | 231/2157 | 77/718 | chr4 | 40750924 | ||
chr4:40776129
|
C | T | 16 | a0001c0001a0001c0013a0003c0003others(13): Show | 283 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
synonymous_variant | LOW | c.906C>T | p.Gly302Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1343/4839 | 906/2157 | 302/718 | chr4 | 40776129 | ||
chr4:40808354
|
T | G | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1572T>G | p.Ala524Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2009/4839 | 1572/2157 | 524/718 | chr4 | 40808354 | ||
chr4:40808372
|
G | T | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1590G>T | p.Leu530Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2027/4839 | 1590/2157 | 530/718 | chr4 | 40808372 | ||
chr4:40808378
|
G | T | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1596G>T | p.Gly532Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2033/4839 | 1596/2157 | 532/718 | chr4 | 40808378 | ||
chr4:40808381
|
T | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1599T>A | p.Ile533Ile | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2036/4839 | 1599/2157 | 533/718 | chr4 | 40808381 | ||
chr4:40808384
|
G | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1602G>A | p.Glu534Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2039/4839 | 1602/2157 | 534/718 | chr4 | 40808384 | ||
chr4:40808387
|
G | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1605G>A | p.Leu535Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2042/4839 | 1605/2157 | 535/718 | chr4 | 40808387 | ||
chr4:40808390
|
T | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1608T>A | p.Gly536Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2045/4839 | 1608/2157 | 536/718 | chr4 | 40808390 | ||
chr4:40808403
|
C | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1621C>A | p.Arg541Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2058/4839 | 1621/2157 | 541/718 | chr4 | 40808403 | ||
chr4:40808405
|
G | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1623G>A | p.Arg541Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2060/4839 | 1623/2157 | 541/718 | chr4 | 40808405 | ||
chr4:40808408
|
G | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1626G>A | p.Glu542Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2063/4839 | 1626/2157 | 542/718 | chr4 | 40808408 | ||
chr4:40808411
|
G | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1629G>A | p.Lys543Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2066/4839 | 1629/2157 | 543/718 | chr4 | 40808411 | ||
chr4:40808417
|
G | A | 1 | a0013c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1635G>A | p.Lys545Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2072/4839 | 1635/2157 | 545/718 | chr4 | 40808417 | ||
chr4:40808606
|
G | A | 1 | a0001c0013 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1824G>A | p.Lys608Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2261/4839 | 1824/2157 | 608/718 | chr4 | 40808606 | ||
chr4:40808717
|
T | C | 1 | a0004c0014 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1935T>C | p.Ala645Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2372/4839 | 1935/2157 | 645/718 | chr4 | 40808717 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:40750042
|
C | T | 1 | a0001c0001t0019 | 2 | HG02258.hp1 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-350C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 652 | chr4 | 40750042 | |||||
chr4:40750081
|
C | T | 2 | a0003c0003t0016a0005c0007t0048 | 4 | HG01358.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-311C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 613 | chr4 | 40750081 | |||||
chr4:40750105
|
C | T | 5 | a0001c0001t0045a0001c0001t0047a0004c0004t0008others(2): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-287C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 589 | chr4 | 40750105 | |||||
chr4:40750136
|
A | AC | 11 | a0001c0001t0005a0001c0001t0017a0001c0001t0020others(8): Show | 21 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-250dupC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 551 | INFO_REALIGN_3_PRIME | chr4 | 40750136 | ||||
chr4:40750233
|
A | G | 1 | a0003c0003t0044 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 461 | chr4 | 40750233 | |||||
chr4:40750687
|
G | A | 1 | a0002c0002t0026 | 1 | HG01975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 7 | chr4 | 40750687 | |||||
chr4:40808961
|
G | A | 6 | a0001c0001t0009a0001c0001t0012a0001c0001t0013others(3): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*22G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 22 | chr4 | 40808961 | |||||
chr4:40809193
|
G | C | 1 | a0005c0007t0028 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 254 | chr4 | 40809193 | |||||
chr4:40809196
|
C | T | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG02602.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*257C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 257 | chr4 | 40809196 | |||||
chr4:40809216
|
T | G | 1 | a0001c0001t0029 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 277 | chr4 | 40809216 | |||||
chr4:40809259
|
G | A | 3 | a0004c0004t0008a0004c0004t0046a0004c0014t0008 | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*320G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 320 | chr4 | 40809259 | |||||
chr4:40809389
|
C | T | 3 | a0001c0001t0007a0001c0001t0041a0019c0009t0007 | 8 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 450 | chr4 | 40809389 | |||||
chr4:40809664
|
A | G | 13 | a0001c0001t0045a0001c0001t0047a0003c0003t0011others(10): Show | 24 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*725A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 725 | chr4 | 40809664 | |||||
chr4:40809726
|
A | AATT | 10 | a0003c0003t0003a0003c0003t0006a0003c0003t0021others(7): Show | 41 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*790dupATT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 791 | INFO_REALIGN_3_PRIME | chr4 | 40809726 | ||||
chr4:40809832
|
A | G | 1 | a0001c0001t0039 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 893 | chr4 | 40809832 | |||||
chr4:40809902
|
A | C | 1 | a0001c0001t0038 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 963 | chr4 | 40809902 | |||||
chr4:40809936
|
A | T | 3 | a0001c0001t0007a0001c0001t0041a0019c0009t0007 | 8 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*997A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 997 | chr4 | 40809936 | |||||
chr4:40810154
|
C | T | 1 | a0001c0001t0027 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1215C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1215 | chr4 | 40810154 | |||||
chr4:40810348
|
C | T | 1 | a0005c0007t0028 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1409C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1409 | chr4 | 40810348 | |||||
chr4:40810357
|
C | T | 1 | a0001c0001t0037 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1418 | chr4 | 40810357 | |||||
chr4:40810494
|
CTT | C | 3 | a0004c0004t0008a0004c0004t0046a0004c0014t0008 | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1556_*1557delTT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1556 | chr4 | 40810494 | |||||
chr4:40810577
|
C | CA | 19 | a0001c0001t0004a0001c0001t0007a0001c0001t0045others(16): Show | 74 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1662dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1663 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | ||||
chr4:40810577
|
C | CAA | 13 | a0001c0001t0012a0001c0001t0014a0001c0001t0020others(10): Show | 25 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1661_*1662dupAA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1663 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | ||||
chr4:40810577
|
C | CAAA | 4 | a0001c0001t0009a0001c0001t0017a0005c0007t0030others(1): Show | 10 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1660_*1662dupAAA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1663 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | ||||
chr4:40810577
|
CA | C | 12 | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(9): Show | 58 | HG00140.hp2 HG00621.hp2 HG00738.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1662delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1662 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | ||||
chr4:40810577
|
CAA | C | 2 | a0001c0001t0010a0002c0002t0010 | 6 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1661_*1662delAA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1661 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | ||||
chr4:40810619
|
A | C | 1 | a0002c0002t0035 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1680 | chr4 | 40810619 | |||||
chr4:40810652
|
T | C | 23 | a0001c0001t0045a0001c0001t0047a0003c0003t0003others(20): Show | 65 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1713T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1713 | chr4 | 40810652 | |||||
chr4:40810705
|
A | G | 1 | a0006c0006t0034 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1766 | chr4 | 40810705 | |||||
chr4:40810723
|
T | G | 1 | a0001c0001t0018 | 2 | NA18983.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1784T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1784 | chr4 | 40810723 | |||||
chr4:40810849
|
G | A | 1 | a0003c0003t0031 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1910G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1910 | chr4 | 40810849 | |||||
chr4:40810892
|
G | C | 1 | a0001c0001t0033 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1953G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1953 | chr4 | 40810892 | |||||
chr4:40810933
|
A | G | 1 | a0001c0001t0036 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1994A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1994 | chr4 | 40810933 | |||||
chr4:40811100
|
T | TATC | 6 | a0001c0001t0045a0001c0001t0047a0004c0004t0008others(3): Show | 11 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2162_*2164dupATC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2165 | INFO_REALIGN_3_PRIME | chr4 | 40811100 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:40750367
|
T | C | 1 | a0008c0008t0005g0020 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-92+67T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | chr4 | 40750367 | ||||||
chr4:40750444
|
C | CT | 15 | a0001c0001t0002g0360a0002c0002t0001g0356a0002c0002t0001g0358others(12): Show | 15 | HG02071.hp2 HG03471.hp1 HG03486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-91-143dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 40750444 | |||||
chr4:40750444
|
CT | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 154 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.-91-143delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 40750444 | |||||
chr4:40750444
|
CTT | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(23): Show | 27 | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.-91-144_-91-143del others(2): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 40750444 | |||||
chr4:40751079
|
T | G | 1 | a0004c0014t0008g0046 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.298+88T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751079 | ||||||
chr4:40751085
|
A | G | 1 | a0003c0003t0006g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.298+94A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751085 | ||||||
chr4:40751138
|
A | G | 1 | a0003c0003t0016g0355 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+147A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751138 | ||||||
chr4:40751155
|
A | T | 1 | a0001c0001t0002g0354 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.298+164A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751155 | ||||||
chr4:40751232
|
G | T | 1 | a0003c0022t0003g0353 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298+241G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751232 | ||||||
chr4:40751289
|
T | C | 4 | a0002c0002t0001g0356a0002c0002t0001g0358a0002c0002t0001g0359others(1): Show | 4 | NA18968.hp1 NA19009.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+298T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751289 | ||||||
chr4:40751380
|
C | A | 1 | a0001c0001t0002g0176 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298+389C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751380 | ||||||
chr4:40751421
|
GC | G | 6 | a0001c0001t0002g0349a0003c0003t0003g0347a0003c0003t0003g0348others(3): Show | 6 | HG01074.hp2 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+432delC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40751421 | |||||
chr4:40751466
|
G | A | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.298+475G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751466 | ||||||
chr4:40751505
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 257 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.298+514G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751505 | ||||||
chr4:40751549
|
G | A | 24 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0048others(21): Show | 24 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.298+558G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751549 | ||||||
chr4:40751569
|
A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.298+578A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751569 | ||||||
chr4:40751610
|
A | T | 1 | a0002c0002t0010g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.298+619A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751610 | ||||||
chr4:40751754
|
G | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.298+763G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751754 | ||||||
chr4:40751763
|
G | A | 3 | a0002c0002t0001g0362a0006c0006t0015g0168a0006c0006t0034g0363 | 3 | HG02559.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+772G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751763 | ||||||
chr4:40751819
|
C | T | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+828C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751819 | ||||||
chr4:40752011
|
GACCAAAT others(10): Show |
G | 1 | a0001c0001t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.298+1021_298+1037d others(19): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752011 | ||||||
chr4:40752068
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0004g0005others(1): Show | 4 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1077G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752068 | ||||||
chr4:40752132
|
A | G | 68 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(65): Show | 69 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.298+1141A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752132 | ||||||
chr4:40752137
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.298+1146C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752137 | ||||||
chr4:40752189
|
C | CCTAAAGA others(3): Show |
1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1206_298+1207i others(12): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40752189 | |||||
chr4:40752200
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1209A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752200 | ||||||
chr4:40752206
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1215A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752206 | ||||||
chr4:40752230
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1239A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752230 | ||||||
chr4:40752231
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1240T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752231 | ||||||
chr4:40752235
|
C | G | 1 | a0002c0002t0004g0333 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.298+1244C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752235 | ||||||
chr4:40752260
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1269T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752260 | ||||||
chr4:40752268
|
C | T | 1 | a0008c0008t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.298+1277C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752268 | ||||||
chr4:40752274
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1283A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752274 | ||||||
chr4:40752275
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1284G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752275 | ||||||
chr4:40752299
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1308A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752299 | ||||||
chr4:40752300
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1309G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752300 | ||||||
chr4:40752301
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1310A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752301 | ||||||
chr4:40752303
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1312G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752303 | ||||||
chr4:40752307
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1316T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752307 | ||||||
chr4:40752308
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1317G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752308 | ||||||
chr4:40752309
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1318G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752309 | ||||||
chr4:40752311
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1320T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752311 | ||||||
chr4:40752312
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1321T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752312 | ||||||
chr4:40752334
|
T | C | 4 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0362others(1): Show | 4 | HG03834.hp1 HG04115.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1343T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752334 | ||||||
chr4:40752339
|
G | A | 1 | a0002c0002t0001g0255 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.298+1348G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752339 | ||||||
chr4:40752485
|
A | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(71): Show | 75 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.298+1494A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752485 | ||||||
chr4:40752608
|
G | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.298+1617G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752608 | ||||||
chr4:40752609
|
A | G | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+1618A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752609 | ||||||
chr4:40752743
|
A | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0154a0001c0001t0001g0155others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+1752A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752743 | ||||||
chr4:40752821
|
A | ATAATGTA others(58): Show |
277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(274): Show | 286 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.298+1830_298+1831i others(67): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752821 | ||||||
chr4:40752821
|
A | ATAATGTG others(58): Show |
1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+1830_298+1831i others(67): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752821 | ||||||
chr4:40752822
|
G | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 287 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.298+1831G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752822 | ||||||
chr4:40752899
|
C | G | 1 | a0001c0001t0047g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.298+1908C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752899 | ||||||
chr4:40753010
|
C | T | 1 | a0002c0002t0004g0329 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.298+2019C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753010 | ||||||
chr4:40753280
|
CT | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 30 | HG00408.hp1 HG01070.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.298+2304delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40753280 | |||||
chr4:40753309
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+2318C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753309 | ||||||
chr4:40753388
|
G | A | 1 | a0002c0002t0001g0257 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.298+2397G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753388 | ||||||
chr4:40753488
|
G | T | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+2497G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753488 | ||||||
chr4:40753507
|
G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+2516G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753507 | ||||||
chr4:40753536
|
G | C | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.298+2545G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753536 | ||||||
chr4:40753695
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.298+2704G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753695 | ||||||
chr4:40753718
|
C | T | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+2727C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753718 | ||||||
chr4:40753894
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+2903C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753894 | ||||||
chr4:40754042
|
A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.298+3051A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754042 | ||||||
chr4:40754134
|
CCTG | C | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+3146_298+3148d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40754134 | |||||
chr4:40754146
|
C | CT | 86 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 89 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.298+3170dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40754146 | |||||
chr4:40754216
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298+3225C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754216 | ||||||
chr4:40754217
|
G | A | 1 | a0001c0001t0038g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.298+3226G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754217 | ||||||
chr4:40754319
|
G | A | 1 | a0003c0003t0003g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.298+3328G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754319 | ||||||
chr4:40754639
|
G | A | 2 | a0001c0013t0002g0153a0012c0015t0040g0174 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+3648G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754639 | ||||||
chr4:40754694
|
C | G | 4 | a0003c0003t0015g0240a0003c0003t0016g0239a0003c0003t0016g0355others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+3703C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754694 | ||||||
chr4:40754738
|
A | G | 3 | a0002c0002t0001g0326a0002c0002t0001g0327a0002c0002t0004g0325 | 3 | HG02129.hp1 NA18965.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.298+3747A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754738 | ||||||
chr4:40754864
|
CCTT | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG01346.hp2 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+3875_298+3877d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40754864 | |||||
chr4:40754881
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 172 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.298+3890A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754881 | ||||||
chr4:40754939
|
C | A | 8 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(5): Show | 8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+3948C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754939 | ||||||
chr4:40754952
|
T | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0337a0001c0001t0002g0176others(13): Show | 17 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.298+3961T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754952 | ||||||
chr4:40755016
|
G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+4025G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755016 | ||||||
chr4:40755143
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+4152G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755143 | ||||||
chr4:40755151
|
G | A | 75 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 78 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+4160G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755151 | ||||||
chr4:40755203
|
C | T | 3 | a0001c0013t0002g0153a0003c0003t0006g0165a0012c0015t0040g0174 | 3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+4212C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755203 | ||||||
chr4:40755244
|
C | T | 1 | a0001c0001t0004g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.298+4253C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755244 | ||||||
chr4:40755250
|
C | T | 1 | a0002c0002t0026g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.298+4259C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755250 | ||||||
chr4:40755279
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.298+4288C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755279 | ||||||
chr4:40755332
|
C | T | 1 | a0003c0003t0015g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.298+4341C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755332 | ||||||
chr4:40755418
|
AT | A | 16 | a0001c0001t0001g0229a0001c0001t0002g0186a0001c0001t0002g0187others(13): Show | 16 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.298+4436delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40755418 | |||||
chr4:40755491
|
T | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+4500T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755491 | ||||||
chr4:40756062
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-4372C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756062 | ||||||
chr4:40756109
|
T | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 181 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.299-4325T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756109 | ||||||
chr4:40756205
|
C | T | 3 | a0001c0013t0002g0153a0003c0003t0006g0165a0012c0015t0040g0174 | 3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-4229C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756205 | ||||||
chr4:40756211
|
A | G | 3 | a0001c0013t0002g0153a0003c0003t0006g0165a0012c0015t0040g0174 | 3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-4223A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756211 | ||||||
chr4:40756257
|
C | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-4177C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756257 | ||||||
chr4:40756289
|
G | A | 1 | a0002c0002t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-4145G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756289 | ||||||
chr4:40756380
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-4054C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756380 | ||||||
chr4:40756398
|
A | G | 1 | a0001c0001t0013g0346 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-4036A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756398 | ||||||
chr4:40756499
|
A | G | 1 | a0003c0003t0003g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.299-3935A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756499 | ||||||
chr4:40756508
|
A | G | 22 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(19): Show | 22 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-3926A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756508 | ||||||
chr4:40756686
|
A | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-3748A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756686 | ||||||
chr4:40756741
|
T | C | 1 | a0002c0002t0001g0362 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-3693T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756741 | ||||||
chr4:40756845
|
AAAAGCT | A | 6 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-3587_299-3582d others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40756845 | |||||
chr4:40757178
|
G | A | 1 | a0001c0001t0007g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.299-3256G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757178 | ||||||
chr4:40757231
|
TAAATAAA others(5): Show |
T | 1 | a0001c0001t0001g0010 | 2 | NA19083.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.299-3184_299-3173d others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757231 | |||||
chr4:40757298
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-3136G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757298 | ||||||
chr4:40757493
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-2941A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757493 | ||||||
chr4:40757535
|
TTA | T | 3 | a0001c0001t0001g0259a0003c0003t0006g0370a0003c0003t0015g0240 | 3 | HG01099.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-2884_299-2883d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757535 | |||||
chr4:40757544
|
TATATATA others(25): Show |
T | 8 | a0004c0004t0008g0068a0004c0004t0008g0069a0004c0004t0008g0070others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-2882_299-2851d others(34): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757544 | |||||
chr4:40757552
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-2882A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757552 | ||||||
chr4:40757556
|
T | TTA | 3 | a0001c0013t0002g0153a0003c0003t0006g0165a0012c0015t0040g0174 | 3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-2865_299-2864d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757556 | |||||
chr4:40757579
|
ATATATAT others(12): Show |
A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-2846_299-2828d others(21): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757579 | |||||
chr4:40757588
|
C | CACATTGT others(12): Show |
1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-2825_299-2807d others(21): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757588 | |||||
chr4:40757588
|
CACATTGT others(33): Show |
C | 1 | a0001c0001t0007g0242 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-2817_299-2778d others(42): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757588 | |||||
chr4:40757594
|
GTGTGTAT others(50): Show |
G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-2806_299-2750d others(59): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757594 | |||||
chr4:40757628
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 178 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.299-2806T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757628 | ||||||
chr4:40757651
|
T | TTGTGTGT others(35): Show |
1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-2778_299-2777i others(44): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757651 | |||||
chr4:40757657
|
A | G | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-2777A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757657 | ||||||
chr4:40757664
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-2770T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757664 | ||||||
chr4:40757668
|
T | C | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2766T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757668 | ||||||
chr4:40757689
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-2745C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757689 | ||||||
chr4:40757697
|
A | T | 1 | a0006c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-2737A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757697 | ||||||
chr4:40757725
|
T | C | 2 | a0002c0002t0001g0257a0002c0002t0001g0260 | 2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.299-2709T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757725 | ||||||
chr4:40757725
|
T | TATAC | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2708_299-2707i others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757725 | |||||
chr4:40757725
|
TAC | T | 20 | a0001c0001t0001g0019a0001c0001t0001g0337a0001c0001t0002g0176others(17): Show | 21 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-2685_299-2684d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757725 | |||||
chr4:40757725
|
TACAC | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 251 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.299-2687_299-2684d others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757725 | |||||
chr4:40757727
|
C | T | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-2707C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757727 | ||||||
chr4:40757729
|
C | T | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-2705C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757729 | ||||||
chr4:40757731
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 169 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.299-2703C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757731 | ||||||
chr4:40757902
|
T | G | 4 | a0001c0013t0002g0153a0003c0003t0006g0165a0012c0015t0040g0174others(1): Show | 4 | HG02559.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-2532T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757902 | ||||||
chr4:40757902
|
T | TTTTG | 33 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0138others(30): Show | 34 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.299-2504_299-2501d others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757902 | |||||
chr4:40757902
|
T | TTTTGTTT others(1): Show |
205 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 213 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.299-2508_299-2501d others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757902 | |||||
chr4:40757902
|
T | TTTTGTTT others(5): Show |
27 | a0001c0001t0001g0079a0001c0001t0001g0149a0001c0001t0001g0179others(24): Show | 27 | HG00735.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.299-2512_299-2501d others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757902 | |||||
chr4:40758135
|
G | A | 2 | a0002c0002t0001g0262a0002c0002t0004g0261 | 2 | NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.299-2299G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758135 | ||||||
chr4:40758142
|
A | G | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-2292A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758142 | ||||||
chr4:40758157
|
T | C | 1 | a0001c0001t0013g0334 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.299-2277T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758157 | ||||||
chr4:40758316
|
A | C | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-2118A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758316 | ||||||
chr4:40758426
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.299-2008C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758426 | ||||||
chr4:40758654
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299-1780A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758654 | ||||||
chr4:40758717
|
A | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0195 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.299-1717A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758717 | ||||||
chr4:40759028
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-1406C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759028 | ||||||
chr4:40759075
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-1359C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759075 | ||||||
chr4:40759096
|
G | A | 2 | a0001c0013t0002g0153a0012c0015t0040g0174 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-1338G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759096 | ||||||
chr4:40759281
|
G | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-1153G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759281 | ||||||
chr4:40759285
|
G | A | 3 | a0003c0003t0003g0029a0003c0003t0003g0030a0003c0003t0003g0231 | 3 | HG00733.hp2 HG01261.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.299-1149G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759285 | ||||||
chr4:40759302
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-1132C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759302 | ||||||
chr4:40759329
|
A | T | 6 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-1105A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759329 | ||||||
chr4:40759415
|
A | T | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.299-1019A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759415 | ||||||
chr4:40759715
|
C | G | 1 | a0002c0002t0001g0324 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-719C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759715 | ||||||
chr4:40759792
|
G | T | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.299-642G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759792 | ||||||
chr4:40759926
|
A | C | 1 | a0001c0001t0004g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.299-508A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759926 | ||||||
chr4:40759969
|
C | T | 3 | a0001c0013t0002g0153a0003c0003t0006g0165a0012c0015t0040g0174 | 3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-465C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759969 | ||||||
chr4:40759979
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 284 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.299-455A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759979 | ||||||
chr4:40760027
|
G | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 272 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.299-407G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760027 | ||||||
chr4:40760184
|
G | T | 3 | a0001c0001t0010g0225a0001c0001t0019g0223a0001c0001t0019g0224 | 3 | HG02258.hp1 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.299-250G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760184 | ||||||
chr4:40760217
|
T | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-217T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760217 | ||||||
chr4:40760228
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-206G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760228 | ||||||
chr4:40760400
|
A | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-34A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760400 | ||||||
chr4:40760610
|
C | T | 3 | a0002c0002t0010g0135a0002c0002t0010g0144a0002c0002t0010g0166 | 3 | HG02717.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.357+118C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760610 | ||||||
chr4:40760687
|
A | AC | 18 | a0001c0001t0039g0230a0001c0001t0045g0066a0001c0001t0047g0074others(15): Show | 18 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+197dupC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760687 | |||||
chr4:40760692
|
G | T | 17 | a0001c0001t0045g0066a0001c0001t0047g0074a0001c0013t0002g0153others(14): Show | 17 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+200G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760692 | ||||||
chr4:40760730
|
A | C | 1 | a0002c0002t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.357+238A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760730 | ||||||
chr4:40760730
|
A | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(145): Show | 153 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.357+238A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760730 | ||||||
chr4:40760732
|
A | G | 1 | a0003c0003t0003g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.357+240A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760732 | ||||||
chr4:40760778
|
T | C | 7 | a0001c0001t0002g0184a0001c0001t0002g0190a0001c0001t0002g0191others(4): Show | 7 | HG01070.hp1 HG01074.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+286T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760778 | ||||||
chr4:40760816
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.357+324T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760816 | ||||||
chr4:40760819
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 146 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.357+327G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760819 | ||||||
chr4:40760862
|
C | CA | 31 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0095others(28): Show | 31 | HG00642.hp2 HG00733.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.358-290dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760862 | |||||
chr4:40760862
|
CA | C | 21 | a0001c0001t0001g0111a0001c0001t0001g0143a0001c0001t0002g0219others(18): Show | 21 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.358-290delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760862 | |||||
chr4:40760911
|
CTCTTAAA | C | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-251_358-245del others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760911 | |||||
chr4:40760983
|
C | G | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-188C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760983 | ||||||
chr4:40760996
|
G | GT | 10 | a0001c0001t0001g0094a0001c0001t0007g0241a0001c0001t0007g0242others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-165dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760996 | |||||
chr4:40761121
|
G | A | 6 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(3): Show | 6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-50G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40761121 | ||||||
chr4:40761151
|
T | A | 1 | a0002c0002t0004g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.358-20T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40761151 | ||||||
chr4:40761153
|
T | A | 1 | a0002c0002t0004g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.358-18T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40761153 | ||||||
chr4:40761305
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.488+4A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761305 | ||||||
chr4:40761449
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.488+148A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761449 | ||||||
chr4:40761600
|
A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+299A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761600 | ||||||
chr4:40761750
|
A | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+449A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761750 | ||||||
chr4:40761757
|
T | C | 63 | a0001c0001t0001g0015a0001c0001t0001g0137a0001c0001t0001g0199others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.488+456T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761757 | ||||||
chr4:40762143
|
A | T | 8 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(5): Show | 8 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+842A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40762143 | ||||||
chr4:40762402
|
C | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.488+1101C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40762402 | ||||||
chr4:40762773
|
T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+1472T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40762773 | ||||||
chr4:40762798
|
G | GATTGTGA others(28): Show |
1 | a0003c0003t0003g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.488+1500_488+1534d others(37): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40762798 | |||||
chr4:40762869
|
A | AGATGATC others(22): Show |
18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+1605_488+1633d others(31): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40762869 | |||||
chr4:40763119
|
G | T | 1 | a0002c0002t0014g0314 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.488+1818G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763119 | ||||||
chr4:40763318
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.488+2017T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763318 | ||||||
chr4:40763403
|
T | TTGG | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 296 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.488+2103_488+2105d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40763403 | |||||
chr4:40763413
|
A | T | 1 | a0001c0001t0002g0218 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.488+2112A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763413 | ||||||
chr4:40763447
|
C | T | 9 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(6): Show | 9 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.488+2146C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763447 | ||||||
chr4:40763448
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.488+2147G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763448 | ||||||
chr4:40763448
|
G | C | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+2147G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763448 | ||||||
chr4:40763455
|
T | C | 1 | a0002c0002t0001g0356 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.488+2154T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763455 | ||||||
chr4:40763609
|
A | T | 1 | a0001c0001t0013g0341 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.488+2308A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763609 | ||||||
chr4:40763640
|
A | C | 8 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(5): Show | 8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+2339A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763640 | ||||||
chr4:40763735
|
C | T | 1 | a0002c0002t0001g0359 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.488+2434C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763735 | ||||||
chr4:40764049
|
T | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+2748T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764049 | ||||||
chr4:40764056
|
T | A | 18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+2755T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764056 | ||||||
chr4:40764064
|
T | A | 1 | a0001c0001t0018g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.488+2763T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764064 | ||||||
chr4:40764074
|
AT | A | 8 | a0004c0004t0008g0068a0004c0004t0008g0069a0004c0004t0008g0070others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+2780delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40764074 | |||||
chr4:40764081
|
T | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+2780T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764081 | ||||||
chr4:40764113
|
C | A | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+2812C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764113 | ||||||
chr4:40764227
|
C | A | 18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+2926C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764227 | ||||||
chr4:40764228
|
T | C | 2 | a0002c0002t0001g0257a0002c0002t0001g0277 | 2 | HG00544.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.488+2927T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764228 | ||||||
chr4:40764228
|
T | TC | 9 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0259others(6): Show | 9 | HG01099.hp2 HG01255.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.488+2933dupC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40764228 | |||||
chr4:40764348
|
C | T | 7 | a0003c0003t0003g0217a0003c0003t0003g0226a0003c0003t0015g0240others(4): Show | 7 | HG00140.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+3047C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764348 | ||||||
chr4:40764350
|
A | C | 4 | a0003c0003t0015g0240a0003c0003t0016g0239a0003c0003t0016g0355others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+3049A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764350 | ||||||
chr4:40764455
|
A | T | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.488+3154A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764455 | ||||||
chr4:40764480
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0154a0001c0001t0001g0155others(14): Show | 17 | HG01891.hp2 HG02280.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.488+3179C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764480 | ||||||
chr4:40764481
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.488+3180G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764481 | ||||||
chr4:40764597
|
T | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.488+3296T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764597 | ||||||
chr4:40764598
|
A | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.488+3297A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764598 | ||||||
chr4:40764600
|
C | T | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+3299C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764600 | ||||||
chr4:40764698
|
A | G | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+3397A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764698 | ||||||
chr4:40764765
|
T | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.488+3464T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764765 | ||||||
chr4:40764766
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488+3465G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764766 | ||||||
chr4:40764900
|
A | G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488+3599A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764900 | ||||||
chr4:40764921
|
G | A | 1 | a0005c0007t0048g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.488+3620G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764921 | ||||||
chr4:40764960
|
A | G | 1 | a0002c0002t0001g0367 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.488+3659A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764960 | ||||||
chr4:40765035
|
G | A | 2 | a0003c0003t0003g0237a0003c0003t0031g0031 | 2 | HG01255.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.488+3734G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765035 | ||||||
chr4:40765087
|
A | G | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+3786A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765087 | ||||||
chr4:40765138
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.488+3837G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765138 | ||||||
chr4:40765221
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.488+3920G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765221 | ||||||
chr4:40765307
|
A | C | 1 | a0003c0003t0011g0163 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.488+4006A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765307 | ||||||
chr4:40765362
|
C | G | 1 | a0003c0003t0016g0361 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488+4061C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765362 | ||||||
chr4:40765402
|
G | A | 2 | a0001c0001t0004g0244a0001c0001t0007g0243 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.488+4101G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765402 | ||||||
chr4:40765513
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.488+4212G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765513 | ||||||
chr4:40765670
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.488+4369G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765670 | ||||||
chr4:40765688
|
C | T | 1 | a0002c0002t0005g0323 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.488+4387C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765688 | ||||||
chr4:40765734
|
C | G | 1 | a0001c0001t0009g0345 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.488+4433C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765734 | ||||||
chr4:40765737
|
G | T | 1 | a0001c0001t0009g0345 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.488+4436G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765737 | ||||||
chr4:40765790
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.488+4489C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765790 | ||||||
chr4:40765864
|
A | G | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+4563A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765864 | ||||||
chr4:40765873
|
C | T | 1 | a0002c0002t0001g0310 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.488+4572C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765873 | ||||||
chr4:40765893
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.488+4592G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765893 | ||||||
chr4:40765943
|
C | T | 71 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.488+4642C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765943 | ||||||
chr4:40766064
|
A | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+4763A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766064 | ||||||
chr4:40766286
|
C | T | 2 | a0001c0001t0009g0193a0001c0001t0017g0180 | 2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.488+4985C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766286 | ||||||
chr4:40766291
|
AG | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.488+4993delG | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40766291 | |||||
chr4:40766416
|
A | G | 10 | a0001c0001t0039g0230a0003c0003t0006g0049a0003c0003t0006g0059others(7): Show | 10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+5115A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766416 | ||||||
chr4:40766506
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488+5205G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766506 | ||||||
chr4:40766673
|
G | A | 4 | a0003c0003t0015g0240a0003c0003t0016g0239a0003c0003t0016g0355others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+5372G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766673 | ||||||
chr4:40766705
|
C | T | 1 | a0003c0003t0006g0369 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.488+5404C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766705 | ||||||
chr4:40766752
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.488+5451G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766752 | ||||||
chr4:40767061
|
G | C | 2 | a0002c0002t0001g0362a0002c0002t0010g0096 | 2 | HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.488+5760G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767061 | ||||||
chr4:40767310
|
G | A | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+6009G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767310 | ||||||
chr4:40767367
|
T | C | 2 | a0001c0001t0002g0198a0001c0001t0002g0219 | 2 | NA19063.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.488+6066T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767367 | ||||||
chr4:40767412
|
C | T | 1 | a0002c0002t0001g0362 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.488+6111C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767412 | ||||||
chr4:40767893
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.489-6372C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767893 | ||||||
chr4:40767918
|
G | A | 1 | a0003c0003t0003g0347 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.489-6347G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767918 | ||||||
chr4:40768109
|
G | T | 4 | a0002c0002t0001g0012a0002c0002t0001g0169a0002c0002t0002g0012others(1): Show | 4 | NA18993.hp2 NA19011.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-6156G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768109 | ||||||
chr4:40768204
|
C | CT | 9 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0139others(6): Show | 9 | NA18944.hp1 NA18985.hp2 NA18988.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-6046dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40768204 | |||||
chr4:40768204
|
CT | C | 71 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0050others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.489-6046delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40768204 | |||||
chr4:40768208
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.489-6057T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768208 | ||||||
chr4:40768209
|
T | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG02257.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-6056T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768209 | ||||||
chr4:40768240
|
C | T | 2 | a0003c0003t0006g0165a0003c0003t0006g0370 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.489-6025C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768240 | ||||||
chr4:40768436
|
C | T | 14 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(11): Show | 14 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.489-5829C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768436 | ||||||
chr4:40768486
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489-5779G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768486 | ||||||
chr4:40768669
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.489-5596G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768669 | ||||||
chr4:40768966
|
C | G | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489-5299C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768966 | ||||||
chr4:40769076
|
C | G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489-5189C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769076 | ||||||
chr4:40769253
|
T | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.489-5012T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769253 | ||||||
chr4:40769322
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489-4943T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769322 | ||||||
chr4:40769347
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489-4918A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769347 | ||||||
chr4:40769375
|
C | T | 1 | a0002c0002t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.489-4890C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769375 | ||||||
chr4:40769376
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.489-4889G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769376 | ||||||
chr4:40769519
|
G | A | 2 | a0003c0003t0006g0165a0003c0003t0006g0370 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.489-4746G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769519 | ||||||
chr4:40769673
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 139 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.489-4592T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769673 | ||||||
chr4:40769714
|
A | G | 8 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(5): Show | 8 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-4551A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769714 | ||||||
chr4:40769815
|
C | T | 1 | a0008c0008t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489-4450C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769815 | ||||||
chr4:40769908
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-4357C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769908 | ||||||
chr4:40769975
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489-4290C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769975 | ||||||
chr4:40769983
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489-4282G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769983 | ||||||
chr4:40769990
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489-4275T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769990 | ||||||
chr4:40769997
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489-4268G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769997 | ||||||
chr4:40769997
|
G | T | 1 | a0003c0003t0003g0030 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.489-4268G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769997 | ||||||
chr4:40770012
|
C | A | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.489-4253C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770012 | ||||||
chr4:40770070
|
C | T | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-4195C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770070 | ||||||
chr4:40770094
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489-4171T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770094 | ||||||
chr4:40770188
|
T | A | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.489-4077T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770188 | ||||||
chr4:40770210
|
C | CA | 12 | a0001c0001t0045g0066a0001c0001t0047g0074a0002c0002t0001g0280others(9): Show | 12 | HG02071.hp2 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.489-4036dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40770210 | |||||
chr4:40770210
|
CA | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(236): Show | 248 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.489-4036delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40770210 | |||||
chr4:40770210
|
CAA | C | 14 | a0001c0001t0001g0075a0001c0001t0001g0084a0001c0001t0001g0107others(11): Show | 14 | HG01070.hp1 HG01070.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.489-4037_489-4036d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40770210 | |||||
chr4:40770230
|
G | A | 1 | a0002c0002t0001g0279 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.489-4035G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770230 | ||||||
chr4:40770284
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489-3981G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770284 | ||||||
chr4:40770446
|
A | G | 1 | a0003c0003t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.489-3819A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770446 | ||||||
chr4:40770497
|
C | T | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-3768C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770497 | ||||||
chr4:40770532
|
G | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 131 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.489-3733G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770532 | ||||||
chr4:40770934
|
C | T | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-3331C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770934 | ||||||
chr4:40770942
|
T | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 194 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.489-3323T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770942 | ||||||
chr4:40770983
|
G | A | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-3282G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770983 | ||||||
chr4:40771046
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489-3219C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771046 | ||||||
chr4:40771183
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.489-3082G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771183 | ||||||
chr4:40771241
|
T | C | 9 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(6): Show | 9 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-3024T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771241 | ||||||
chr4:40771260
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-3005C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771260 | ||||||
chr4:40771265
|
A | G | 1 | a0002c0002t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.489-3000A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771265 | ||||||
chr4:40771500
|
A | C | 1 | a0001c0001t0009g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.489-2765A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771500 | ||||||
chr4:40771591
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.489-2674T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771591 | ||||||
chr4:40771648
|
C | A | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.489-2617C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771648 | ||||||
chr4:40771662
|
A | C | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.489-2603A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771662 | ||||||
chr4:40771745
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-2520A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771745 | ||||||
chr4:40771842
|
T | C | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489-2423T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771842 | ||||||
chr4:40771952
|
A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.489-2313A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771952 | ||||||
chr4:40772059
|
C | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.489-2206C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772059 | ||||||
chr4:40772073
|
C | A | 2 | a0002c0002t0001g0253a0002c0002t0001g0254 | 2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.489-2192C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772073 | ||||||
chr4:40772665
|
A | T | 2 | a0001c0001t0001g0026a0009c0023t0001g0027 | 2 | HG00408.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.489-1600A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772665 | ||||||
chr4:40772716
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 163 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.489-1549C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772716 | ||||||
chr4:40772815
|
A | C | 1 | a0003c0003t0003g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.489-1450A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772815 | ||||||
chr4:40773020
|
G | A | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.489-1245G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773020 | ||||||
chr4:40773117
|
C | T | 3 | a0002c0002t0001g0262a0002c0002t0001g0321a0002c0002t0004g0261 | 3 | NA18961.hp1 NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.489-1148C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773117 | ||||||
chr4:40773176
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(279): Show | 291 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.489-1089C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773176 | ||||||
chr4:40773420
|
C | T | 2 | a0002c0002t0001g0362a0002c0002t0010g0096 | 2 | HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.489-845C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773420 | ||||||
chr4:40773421
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 194 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.489-844G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773421 | ||||||
chr4:40773503
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.489-762C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773503 | ||||||
chr4:40773661
|
C | T | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.489-604C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773661 | ||||||
chr4:40773682
|
C | CA | 11 | a0001c0001t0002g0205a0001c0001t0045g0066a0001c0001t0047g0074others(8): Show | 11 | HG02280.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.489-568dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40773682 | |||||
chr4:40773682
|
CA | C | 11 | a0001c0001t0001g0058a0001c0001t0001g0183a0001c0001t0004g0244others(8): Show | 11 | HG01934.hp2 HG02486.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.489-568delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40773682 | |||||
chr4:40773724
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.489-541C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773724 | ||||||
chr4:40773947
|
C | T | 10 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-318C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773947 | ||||||
chr4:40773991
|
T | G | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-274T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773991 | ||||||
chr4:40774084
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.489-181C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40774084 | ||||||
chr4:40774511
|
C | A | 1 | a0002c0002t0005g0311 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.641+94C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/11 | chr4 | 40774511 | ||||||
chr4:40774516
|
C | T | 1 | a0003c0003t0016g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.641+99C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/11 | chr4 | 40774516 | ||||||
chr4:40774686
|
T | G | 4 | a0001c0001t0001g0229a0001c0001t0002g0186a0001c0001t0002g0187others(1): Show | 4 | NA18944.hp2 NA18975.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-81T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/11 | chr4 | 40774686 | ||||||
chr4:40774961
|
A | G | 7 | a0002c0002t0001g0362a0002c0002t0010g0096a0002c0002t0010g0119others(4): Show | 7 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.825+11A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40774961 | ||||||
chr4:40775063
|
G | A | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.825+113G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775063 | ||||||
chr4:40775130
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 278 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.825+180G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775130 | ||||||
chr4:40775194
|
T | A | 1 | a0007c0005t0001g0282 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.825+244T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775194 | ||||||
chr4:40775229
|
C | T | 8 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(5): Show | 8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.825+279C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775229 | ||||||
chr4:40775318
|
A | G | 1 | a0002c0002t0001g0280 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.825+368A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775318 | ||||||
chr4:40775332
|
A | C | 4 | a0003c0003t0003g0347a0003c0003t0003g0350a0003c0003t0003g0351others(1): Show | 4 | HG01081.hp2 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+382A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775332 | ||||||
chr4:40775430
|
T | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.825+480T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775430 | ||||||
chr4:40775442
|
G | A | 1 | a0003c0003t0006g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.825+492G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775442 | ||||||
chr4:40775453
|
G | A | 4 | a0002c0002t0010g0119a0002c0002t0010g0135a0002c0002t0010g0144others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.825+503G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775453 | ||||||
chr4:40775785
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.826-264A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775785 | ||||||
chr4:40775928
|
C | G | 1 | a0003c0003t0022g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.826-121C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775928 | ||||||
chr4:40775929
|
T | C | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826-120T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775929 | ||||||
chr4:40775944
|
C | A | 83 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.826-105C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775944 | ||||||
chr4:40776009
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.826-40C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40776009 | ||||||
chr4:40776315
|
G | A | 3 | a0005c0007t0028g0043a0005c0007t0030g0045a0005c0007t0048g0236 | 3 | HG01243.hp1 HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1036+56G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776315 | ||||||
chr4:40776333
|
A | G | 2 | a0001c0001t0039g0230a0001c0013t0002g0153 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1036+74A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776333 | ||||||
chr4:40776391
|
T | C | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1036+132T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776391 | ||||||
chr4:40776444
|
G | A | 8 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(5): Show | 8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+185G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776444 | ||||||
chr4:40776529
|
GTATCATT others(17): Show |
G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+287_1036+310d others(26): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40776529 | |||||
chr4:40776622
|
C | CT | 5 | a0001c0001t0001g0008a0001c0001t0001g0130a0001c0001t0001g0132others(2): Show | 6 | NA18946.hp1 NA18956.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+374dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40776622 | |||||
chr4:40776693
|
A | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+434A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776693 | ||||||
chr4:40776841
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1036+582C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776841 | ||||||
chr4:40776898
|
G | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1036+639G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776898 | ||||||
chr4:40777094
|
C | T | 1 | a0003c0003t0006g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1036+835C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777094 | ||||||
chr4:40777328
|
T | A | 31 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0120others(28): Show | 32 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1036+1069T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777328 | ||||||
chr4:40777329
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 168 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.1036+1070T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777329 | ||||||
chr4:40777341
|
T | G | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1036+1082T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777341 | ||||||
chr4:40777379
|
C | T | 7 | a0002c0002t0001g0362a0002c0002t0010g0096a0002c0002t0010g0119others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+1120C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777379 | ||||||
chr4:40777462
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+1203C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777462 | ||||||
chr4:40777579
|
G | A | 4 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+1320G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777579 | ||||||
chr4:40777591
|
C | T | 1 | a0003c0003t0003g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1036+1332C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777591 | ||||||
chr4:40777783
|
T | G | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+1524T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777783 | ||||||
chr4:40777784
|
G | T | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+1525G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777784 | ||||||
chr4:40777839
|
A | G | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+1580A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777839 | ||||||
chr4:40777839
|
ATCC | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+1585_1036+158 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40777839 | |||||
chr4:40777951
|
G | A | 71 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1036+1692G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777951 | ||||||
chr4:40778093
|
T | G | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1036+1834T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778093 | ||||||
chr4:40778106
|
C | T | 1 | a0001c0001t0047g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1036+1847C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778106 | ||||||
chr4:40778159
|
G | GA | 7 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(4): Show | 7 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+1903dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40778159 | |||||
chr4:40778347
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 188 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.1036+2088T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778347 | ||||||
chr4:40778420
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1036+2161G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778420 | ||||||
chr4:40778444
|
G | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1036+2185G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778444 | ||||||
chr4:40778493
|
G | A | 2 | a0003c0003t0006g0165a0003c0003t0006g0370 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1036+2234G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778493 | ||||||
chr4:40778623
|
CCT | C | 6 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(3): Show | 6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+2365_1036+236 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778623 | ||||||
chr4:40778626
|
A | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+2367A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778626 | ||||||
chr4:40778627
|
G | A | 6 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(3): Show | 6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+2368G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778627 | ||||||
chr4:40778932
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1036+2673T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778932 | ||||||
chr4:40778971
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 289 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1036+2712G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778971 | ||||||
chr4:40779017
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1036+2758G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779017 | ||||||
chr4:40779094
|
A | C | 2 | a0002c0002t0001g0318a0002c0002t0004g0308 | 2 | NA18956.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1036+2835A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779094 | ||||||
chr4:40779164
|
A | T | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1036+2905A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779164 | ||||||
chr4:40779381
|
A | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+3122A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779381 | ||||||
chr4:40779601
|
C | G | 6 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(3): Show | 6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+3342C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779601 | ||||||
chr4:40779601
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 184 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.1036+3342C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779601 | ||||||
chr4:40779738
|
A | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0075others(24): Show | 29 | HG00558.hp1 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1036+3479A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779738 | ||||||
chr4:40779896
|
A | G | 8 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(5): Show | 8 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+3637A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779896 | ||||||
chr4:40780051
|
C | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 131 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1036+3792C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780051 | ||||||
chr4:40780066
|
C | T | 1 | a0001c0001t0020g0331 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1036+3807C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780066 | ||||||
chr4:40780234
|
C | T | 4 | a0001c0001t0002g0220a0001c0001t0010g0225a0001c0001t0019g0223others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+3975C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780234 | ||||||
chr4:40780269
|
G | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+4010G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780269 | ||||||
chr4:40780282
|
A | AAATC | 18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1036+4047_1036+405 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780282 | |||||
chr4:40780284
|
A | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1036+4025A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780284 | ||||||
chr4:40780317
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0004g0115 | 2 | HG01256.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1036+4058A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780317 | ||||||
chr4:40780489
|
C | T | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1036+4230C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780489 | ||||||
chr4:40780630
|
G | A | 1 | a0001c0001t0004g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1036+4371G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780630 | ||||||
chr4:40780668
|
G | A | 10 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(7): Show | 10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+4409G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780668 | ||||||
chr4:40780669
|
G | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+4410G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780669 | ||||||
chr4:40780728
|
A | G | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+4469A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780728 | ||||||
chr4:40780754
|
T | TAC | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(32): Show | 36 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.1036+4527_1036+452 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | |||||
chr4:40780754
|
T | TACAC | 13 | a0001c0001t0001g0010a0001c0001t0001g0085a0001c0001t0001g0089others(10): Show | 14 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1036+4525_1036+452 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | |||||
chr4:40780754
|
T | TACACAC | 8 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0099others(5): Show | 8 | HG00544.hp1 HG01928.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036+4523_1036+452 others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | |||||
chr4:40780754
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1036+4519_1036+452 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | |||||
chr4:40780754
|
TAC | T | 6 | a0002c0002t0001g0254a0002c0002t0001g0255a0002c0002t0001g0257others(3): Show | 6 | HG00544.hp2 HG01978.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4527_1036+452 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | |||||
chr4:40780754
|
TACAC | T | 2 | a0002c0002t0001g0307a0002c0002t0002g0016 | 3 | HG02886.hp2 NA18906.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1036+4525_1036+452 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | |||||
chr4:40780774
|
CACACACA others(7): Show |
C | 7 | a0001c0001t0047g0074a0004c0004t0008g0070a0004c0004t0008g0071others(4): Show | 7 | HG02280.hp2 HG02630.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+4521_1036+453 others(18): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780774 | |||||
chr4:40780776
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1036+4523_1036+453 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780776 | |||||
chr4:40780778
|
CACACACA others(9): Show |
C | 7 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+4521_1036+453 others(20): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780778 | |||||
chr4:40780782
|
CACACAT | C | 6 | a0002c0002t0001g0268a0002c0002t0001g0269a0002c0002t0001g0270others(3): Show | 6 | HG02074.hp1 NA18943.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4531_1036+453 others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780782 | |||||
chr4:40780782
|
CACACATA others(5): Show |
C | 1 | a0003c0003t0003g0237 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1036+4525_1036+453 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780782 | |||||
chr4:40780782
|
CACACATA others(7): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1036+4525_1036+453 others(18): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780782 | |||||
chr4:40780784
|
CACAT | C | 37 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0201others(34): Show | 37 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1036+4529_1036+453 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780784 | |||||
chr4:40780784
|
CACATACA others(3): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1036+4527_1036+453 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780784 | |||||
chr4:40780784
|
CACATACA others(9): Show |
C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0216others(2): Show | 5 | HG01192.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+4527_1036+454 others(20): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780784 | |||||
chr4:40780786
|
C | T | 1 | a0002c0002t0001g0328 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1036+4527C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780786 | ||||||
chr4:40780786
|
CAT | C | 44 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0048others(41): Show | 45 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1036+4529_1036+453 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780786 | |||||
chr4:40780786
|
CATACACA others(5): Show |
C | 3 | a0001c0001t0002g0208a0001c0001t0002g0219a0010c0021t0002g0083 | 3 | HG02080.hp2 NA19063.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1036+4531_1036+454 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780786 | |||||
chr4:40780786
|
CATACACA others(7): Show |
C | 11 | a0001c0001t0002g0203a0001c0001t0002g0349a0001c0001t0002g0360others(8): Show | 11 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036+4531_1036+454 others(18): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780786 | |||||
chr4:40780788
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 161 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1036+4529T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780788 | ||||||
chr4:40780788
|
TACAC | T | 3 | a0002c0002t0001g0256a0002c0002t0001g0267a0002c0002t0001g0272 | 3 | NA18949.hp2 NA18957.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1036+4531_1036+453 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780788 | |||||
chr4:40780790
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0033g0081a0002c0002t0001g0266 | 3 | HG03139.hp2 HG03540.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1036+4531C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780790 | ||||||
chr4:40780790
|
CACATATA others(3): Show |
C | 1 | a0001c0001t0002g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1036+4533_1036+454 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780790 | |||||
chr4:40780790
|
CACATATA others(5): Show |
C | 1 | a0001c0001t0001g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1036+4533_1036+454 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780790 | |||||
chr4:40780792
|
C | CAT | 6 | a0002c0002t0001g0002a0002c0002t0001g0278a0002c0002t0001g0288others(3): Show | 8 | HG00438.hp2 HG04115.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036+4554_1036+455 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780792 | |||||
chr4:40780792
|
C | T | 6 | a0001c0001t0039g0230a0001c0001t0045g0066a0002c0002t0001g0266others(3): Show | 6 | HG00438.hp1 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+4533C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780792 | ||||||
chr4:40780792
|
CATAT | C | 3 | a0001c0001t0001g0179a0003c0003t0011g0162a0003c0003t0025g0161 | 3 | HG01123.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1036+4552_1036+455 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780792 | |||||
chr4:40780794
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 130 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1036+4535T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780794 | ||||||
chr4:40780796
|
T | C | 91 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(88): Show | 93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1036+4537T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780796 | ||||||
chr4:40780798
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 109 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1036+4539T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780798 | ||||||
chr4:40780800
|
T | C | 37 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0098others(34): Show | 37 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1036+4541T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780800 | ||||||
chr4:40780802
|
T | C | 5 | a0001c0001t0001g0316a0001c0001t0002g0360a0001c0001t0018g0024others(2): Show | 5 | HG00423.hp1 HG01074.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+4543T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780802 | ||||||
chr4:40780803
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+4546_1036+455 others(17): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780803 | |||||
chr4:40780804
|
T | C | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1036+4545T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780804 | ||||||
chr4:40780804
|
TATATATA others(2): Show |
T | 31 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0201others(28): Show | 31 | HG00597.hp2 HG01070.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1036+4546_1036+455 others(13): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780804 | ||||||
chr4:40780805
|
ATATATAT others(2): Show |
A | 8 | a0001c0001t0002g0063a0001c0001t0002g0196a0001c0001t0002g0197others(5): Show | 8 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036+4548_1036+455 others(13): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780805 | |||||
chr4:40780805
|
ATATATAT others(3): Show |
A | 1 | a0003c0003t0003g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1036+4548_1036+455 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780805 | |||||
chr4:40780805
|
ATATATAT others(5): Show |
A | 3 | a0001c0001t0007g0241a0001c0001t0007g0246a0001c0001t0007g0247 | 3 | NA18995.hp2 NA19004.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1036+4548_1036+455 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780805 | |||||
chr4:40780807
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0007g0242 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1036+4550_1036+456 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780807 | |||||
chr4:40780809
|
ATATATTT others(5): Show |
A | 1 | a0001c0001t0007g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1036+4552_1036+456 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780809 | |||||
chr4:40780811
|
A | T | 1 | a0002c0002t0001g0304 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1036+4552A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780811 | ||||||
chr4:40780811
|
ATAT | A | 15 | a0001c0001t0001g0025a0001c0001t0001g0026a0003c0003t0003g0028others(12): Show | 15 | HG00408.hp1 HG00733.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1036+4554_1036+455 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780811 | |||||
chr4:40780812
|
TA | T | 15 | a0001c0001t0001g0057a0001c0001t0001g0172a0001c0001t0002g0203others(12): Show | 15 | HG00738.hp1 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1036+4554delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780812 | ||||||
chr4:40780813
|
A | AT | 8 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0284others(5): Show | 8 | HG02559.hp2 HG03834.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+4578dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | |||||
chr4:40780813
|
A | T | 17 | a0001c0001t0002g0112a0001c0001t0002g0219a0001c0001t0036g0215others(14): Show | 17 | HG00597.hp1 HG01192.hp1 HG03209.hp2 others(14): Show |
intron_variant | MODIFIER | c.1036+4554A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780813 | ||||||
chr4:40780813
|
AT | A | 24 | a0001c0001t0001g0145a0001c0001t0002g0102a0001c0001t0002g0349others(21): Show | 24 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1036+4578delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | |||||
chr4:40780813
|
ATT | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(39): Show | 45 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1036+4577_1036+457 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | |||||
chr4:40780813
|
ATTT | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0143others(3): Show | 6 | HG00558.hp1 HG01358.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+4576_1036+457 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | |||||
chr4:40780813
|
ATTTT | A | 6 | a0002c0002t0001g0362a0002c0002t0010g0096a0002c0002t0010g0135others(3): Show | 6 | HG02055.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4575_1036+457 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | |||||
chr4:40780814
|
T | TA | 5 | a0001c0001t0001g0090a0001c0001t0004g0115a0001c0001t0009g0338others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+4555_1036+455 others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780814 | ||||||
chr4:40780814
|
T | TATA | 3 | a0001c0001t0001g0076a0001c0001t0001g0316a0002c0002t0001g0287 | 3 | HG00423.hp1 HG01346.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1036+4555_1036+455 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780814 | ||||||
chr4:40780815
|
T | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 71 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1036+4556T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780815 | ||||||
chr4:40780816
|
T | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0316a0001c0001t0004g0115others(4): Show | 7 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+4557T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780816 | ||||||
chr4:40780817
|
T | A | 25 | a0001c0001t0001g0113a0001c0001t0001g0123a0001c0001t0001g0124others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1036+4558T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780817 | ||||||
chr4:40780818
|
T | A | 2 | a0001c0001t0009g0338a0002c0002t0010g0119 | 2 | HG02004.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1036+4559T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780818 | ||||||
chr4:40780819
|
T | A | 3 | a0001c0001t0012g0175a0012c0015t0040g0174a0019c0009t0007g0332 | 3 | HG02280.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1036+4560T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780819 | ||||||
chr4:40780820
|
T | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1036+4561T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780820 | ||||||
chr4:40780859
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+4600G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780859 | ||||||
chr4:40780868
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+4609G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780868 | ||||||
chr4:40780889
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+4630G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780889 | ||||||
chr4:40780922
|
C | A | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1036+4663C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780922 | ||||||
chr4:40780926
|
T | G | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1036+4667T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780926 | ||||||
chr4:40781064
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1036+4805C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781064 | ||||||
chr4:40781098
|
C | A | 1 | a0002c0002t0002g0016 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1036+4839C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781098 | ||||||
chr4:40781181
|
C | T | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+4922C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781181 | ||||||
chr4:40781256
|
G | T | 1 | a0003c0003t0022g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1036+4997G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781256 | ||||||
chr4:40781263
|
T | C | 14 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(11): Show | 14 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1036+5004T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781263 | ||||||
chr4:40781447
|
T | G | 1 | a0001c0001t0002g0196 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1036+5188T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781447 | ||||||
chr4:40781520
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1036+5261C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781520 | ||||||
chr4:40781553
|
A | C | 2 | a0003c0003t0006g0165a0003c0003t0006g0370 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1036+5294A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781553 | ||||||
chr4:40781612
|
A | G | 1 | a0002c0002t0001g0328 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1036+5353A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781612 | ||||||
chr4:40781824
|
AG | A | 7 | a0002c0002t0001g0362a0002c0002t0010g0096a0002c0002t0010g0119others(4): Show | 7 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+5566delG | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781824 | ||||||
chr4:40782139
|
C | T | 7 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(4): Show | 7 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+5880C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782139 | ||||||
chr4:40782236
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1036+5977A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782236 | ||||||
chr4:40782327
|
C | A | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1036+6068C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782327 | ||||||
chr4:40782327
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA19064.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1036+6068C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782327 | ||||||
chr4:40782392
|
C | T | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+6133C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782392 | ||||||
chr4:40782430
|
T | G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+6171T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782430 | ||||||
chr4:40782547
|
CA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 157 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1036+6303delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40782547 | |||||
chr4:40782564
|
A | G | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+6305A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782564 | ||||||
chr4:40782609
|
C | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+6350C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782609 | ||||||
chr4:40782791
|
C | T | 1 | a0003c0003t0003g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1036+6532C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782791 | ||||||
chr4:40782921
|
G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1036+6662G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782921 | ||||||
chr4:40783088
|
T | G | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1036+6829T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783088 | ||||||
chr4:40783157
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1036+6898C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783157 | ||||||
chr4:40783229
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 188 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.1036+6970A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783229 | ||||||
chr4:40783404
|
T | C | 8 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(5): Show | 8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+7145T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783404 | ||||||
chr4:40783487
|
G | GA | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 276 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.1037-7109dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40783487 | |||||
chr4:40783545
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0154a0001c0001t0001g0155others(2): Show | 5 | HG01891.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-7057T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783545 | ||||||
chr4:40783715
|
G | A | 1 | a0003c0003t0006g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1037-6887G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783715 | ||||||
chr4:40783724
|
G | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-6878G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783724 | ||||||
chr4:40783846
|
TA | T | 10 | a0001c0001t0001g0058a0001c0001t0001g0132a0001c0001t0002g0219others(7): Show | 10 | HG01074.hp1 HG01074.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-6741delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40783846 | |||||
chr4:40783847
|
A | T | 66 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1037-6755A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783847 | ||||||
chr4:40783848
|
A | T | 4 | a0001c0001t0002g0219a0001c0001t0002g0349a0001c0001t0041g0248others(1): Show | 4 | HG01074.hp1 HG01074.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-6754A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783848 | ||||||
chr4:40784092
|
T | C | 1 | a0003c0003t0003g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1037-6510T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784092 | ||||||
chr4:40784175
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1037-6427G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784175 | ||||||
chr4:40784318
|
T | C | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1037-6284T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784318 | ||||||
chr4:40784331
|
A | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0075others(24): Show | 29 | HG00558.hp1 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1037-6271A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784331 | ||||||
chr4:40784439
|
C | T | 5 | a0001c0001t0002g0205a0001c0001t0002g0220a0001c0001t0010g0225others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-6163C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784439 | ||||||
chr4:40784562
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1037-6040C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784562 | ||||||
chr4:40784816
|
T | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-5786T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784816 | ||||||
chr4:40784834
|
G | A | 6 | a0001c0001t0039g0230a0003c0003t0014g0167a0003c0003t0015g0240others(3): Show | 6 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-5768G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784834 | ||||||
chr4:40784942
|
A | G | 11 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(8): Show | 11 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.1037-5660A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784942 | ||||||
chr4:40785035
|
A | AGTT | 5 | a0001c0001t0001g0019a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-5551_1037-554 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40785035 | |||||
chr4:40785129
|
G | T | 1 | a0003c0003t0022g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1037-5473G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785129 | ||||||
chr4:40785138
|
C | G | 1 | a0002c0002t0002g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1037-5464C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785138 | ||||||
chr4:40785201
|
A | AT | 9 | a0001c0001t0001g0021a0001c0001t0001g0098a0002c0002t0001g0254others(6): Show | 9 | HG01258.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1037-5387dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40785201 | |||||
chr4:40785212
|
T | G | 1 | a0001c0001t0005g0100 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1037-5390T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785212 | ||||||
chr4:40785294
|
G | A | 4 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-5308G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785294 | ||||||
chr4:40785362
|
T | C | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-5240T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785362 | ||||||
chr4:40785518
|
G | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 283 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1037-5084G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785518 | ||||||
chr4:40785561
|
A | G | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-5041A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785561 | ||||||
chr4:40785607
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-4995C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785607 | ||||||
chr4:40785641
|
G | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-4961G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785641 | ||||||
chr4:40785676
|
A | AATGAC | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 281 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.1037-4924_1037-492 others(9): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40785676 | |||||
chr4:40785736
|
G | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 289 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1037-4866G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785736 | ||||||
chr4:40785928
|
C | T | 4 | a0003c0003t0015g0240a0003c0003t0016g0239a0003c0003t0016g0355others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-4674C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785928 | ||||||
chr4:40786123
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1037-4479G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786123 | ||||||
chr4:40786193
|
T | C | 75 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1037-4409T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786193 | ||||||
chr4:40786527
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 283 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1037-4075A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786527 | ||||||
chr4:40786662
|
A | G | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-3940A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786662 | ||||||
chr4:40786730
|
T | C | 1 | a0002c0002t0001g0271 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1037-3872T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786730 | ||||||
chr4:40787036
|
G | GA | 32 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1037-3554dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787036 | |||||
chr4:40787036
|
G | GAA | 27 | a0001c0001t0001g0229a0001c0001t0002g0112a0001c0001t0002g0186others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1037-3555_1037-355 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787036 | |||||
chr4:40787036
|
G | GAAA | 6 | a0001c0001t0002g0203a0001c0001t0002g0213a0001c0001t0002g0214others(3): Show | 6 | HG00738.hp1 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-3556_1037-355 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787036 | |||||
chr4:40787044
|
A | G | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-3558A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787044 | ||||||
chr4:40787185
|
G | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-3417G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787185 | ||||||
chr4:40787324
|
C | G | 1 | a0005c0007t0048g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1037-3278C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787324 | ||||||
chr4:40787352
|
A | T | 18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1037-3250A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787352 | ||||||
chr4:40787353
|
AG | A | 18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1037-3248delG | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787353 | ||||||
chr4:40787375
|
AAG | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-3225_1037-322 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787375 | |||||
chr4:40787676
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1037-2926C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787676 | ||||||
chr4:40787858
|
G | A | 1 | a0003c0003t0016g0355 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1037-2744G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787858 | ||||||
chr4:40787897
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1037-2705C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787897 | ||||||
chr4:40787968
|
G | A | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1037-2634G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787968 | ||||||
chr4:40787971
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 186 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.1037-2631A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787971 | ||||||
chr4:40787983
|
G | C | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-2619G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787983 | ||||||
chr4:40788447
|
A | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-2155A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788447 | ||||||
chr4:40788664
|
T | A | 18 | a0001c0001t0001g0337a0001c0001t0009g0193a0001c0001t0009g0335others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1037-1938T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788664 | ||||||
chr4:40788737
|
C | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-1865C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788737 | ||||||
chr4:40788828
|
T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1037-1774T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788828 | ||||||
chr4:40788943
|
C | T | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-1659C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788943 | ||||||
chr4:40789043
|
G | C | 5 | a0001c0001t0001g0229a0001c0001t0002g0186a0001c0001t0002g0187others(2): Show | 5 | NA18944.hp2 NA18975.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-1559G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789043 | ||||||
chr4:40789135
|
C | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 203 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1037-1467C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789135 | ||||||
chr4:40789139
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(153): Show | 165 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.1037-1463C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789139 | ||||||
chr4:40789253
|
T | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1037-1349T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789253 | ||||||
chr4:40789348
|
A | G | 4 | a0003c0003t0003g0347a0003c0003t0003g0350a0003c0003t0003g0351others(1): Show | 4 | HG01081.hp2 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-1254A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789348 | ||||||
chr4:40789355
|
G | A | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-1247G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789355 | ||||||
chr4:40789491
|
G | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-1111G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789491 | ||||||
chr4:40789615
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 284 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1037-987T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789615 | ||||||
chr4:40789705
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1037-897A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789705 | ||||||
chr4:40789930
|
A | G | 5 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-672A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789930 | ||||||
chr4:40789934
|
A | C | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-668A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789934 | ||||||
chr4:40789990
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1037-612G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789990 | ||||||
chr4:40790013
|
T | C | 1 | a0002c0002t0001g0291 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1037-589T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790013 | ||||||
chr4:40790064
|
C | CT | 11 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0087others(8): Show | 11 | HG01169.hp2 HG02818.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1037-520dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | |||||
chr4:40790064
|
C | CTT | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 157 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1037-521_1037-520d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | |||||
chr4:40790064
|
C | CTTT | 12 | a0001c0001t0001g0109a0001c0001t0001g0154a0001c0001t0001g0157others(9): Show | 12 | HG01099.hp2 HG02965.hp1 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.1037-522_1037-520d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | |||||
chr4:40790064
|
C | CTTTT | 15 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(12): Show | 15 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037-523_1037-520d others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | |||||
chr4:40790064
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0033g0081 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1037-538C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790064 | ||||||
chr4:40790064
|
CT | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1037-520delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | |||||
chr4:40790135
|
C | G | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-467C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790135 | ||||||
chr4:40790233
|
T | C | 11 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(8): Show | 11 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1037-369T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790233 | ||||||
chr4:40790323
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1037-279G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790323 | ||||||
chr4:40790324
|
T | C | 1 | a0002c0002t0004g0308 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1037-278T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790324 | ||||||
chr4:40790446
|
G | A | 62 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-156G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790446 | ||||||
chr4:40790482
|
T | A | 13 | a0001c0001t0018g0023a0001c0001t0018g0024a0001c0001t0045g0066others(10): Show | 13 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1037-120T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790482 | ||||||
chr4:40790780
|
T | G | 1 | a0002c0002t0001g0305 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1180+35T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40790780 | ||||||
chr4:40790797
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1180+52A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40790797 | ||||||
chr4:40790908
|
A | G | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1180+163A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40790908 | ||||||
chr4:40791181
|
C | T | 1 | a0001c0001t0019g0223 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1180+436C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791181 | ||||||
chr4:40791214
|
A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1180+469A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791214 | ||||||
chr4:40791432
|
T | C | 1 | a0004c0004t0008g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1180+687T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791432 | ||||||
chr4:40791614
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 140 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1180+869T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791614 | ||||||
chr4:40791691
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1180+946C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791691 | ||||||
chr4:40791743
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1180+998G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791743 | ||||||
chr4:40792039
|
C | T | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1180+1294C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792039 | ||||||
chr4:40792440
|
A | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+1695A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792440 | ||||||
chr4:40792443
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 136 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1180+1698G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792443 | ||||||
chr4:40792445
|
A | G | 1 | a0002c0002t0001g0286 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1180+1700A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792445 | ||||||
chr4:40792477
|
A | C | 36 | a0001c0001t0001g0082a0001c0001t0001g0229a0001c0001t0002g0112others(33): Show | 36 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1180+1732A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792477 | ||||||
chr4:40792480
|
G | C | 4 | a0003c0003t0006g0368a0003c0003t0006g0369a0003c0003t0021g0037others(1): Show | 4 | HG00438.hp1 NA18947.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+1735G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792480 | ||||||
chr4:40792489
|
C | T | 1 | a0002c0002t0001g0235 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1180+1744C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792489 | ||||||
chr4:40792517
|
C | T | 6 | a0001c0001t0001g0181a0001c0001t0007g0241a0001c0001t0007g0242others(3): Show | 6 | HG01952.hp1 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+1772C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792517 | ||||||
chr4:40792522
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 213 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.1180+1777A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792522 | ||||||
chr4:40792545
|
C | A | 13 | a0001c0001t0001g0064a0001c0001t0001g0179a0001c0001t0001g0181others(10): Show | 13 | HG01123.hp2 HG01928.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180+1800C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792545 | ||||||
chr4:40792546
|
T | C | 1 | a0019c0009t0007g0332 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1180+1801T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792546 | ||||||
chr4:40792547
|
C | T | 1 | a0010c0021t0002g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1180+1802C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792547 | ||||||
chr4:40792579
|
G | A | 1 | a0002c0002t0001g0305 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1181-1796G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792579 | ||||||
chr4:40792608
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-1767G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792608 | ||||||
chr4:40792613
|
A | C | 2 | a0003c0003t0015g0158a0003c0003t0015g0240 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1181-1762A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792613 | ||||||
chr4:40792637
|
G | C | 3 | a0002c0002t0001g0017a0002c0002t0001g0279a0016c0011t0004g0366 | 4 | HG02015.hp1 NA18984.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-1738G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792637 | ||||||
chr4:40792668
|
T | C | 1 | a0003c0003t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1181-1707T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792668 | ||||||
chr4:40792668
|
T | G | 5 | a0001c0001t0039g0230a0003c0003t0003g0347a0003c0003t0003g0350others(2): Show | 5 | HG01081.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181-1707T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792668 | ||||||
chr4:40792679
|
G | A | 22 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(19): Show | 22 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1181-1696G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792679 | ||||||
chr4:40792689
|
C | T | 1 | a0002c0002t0002g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1181-1686C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792689 | ||||||
chr4:40792707
|
G | C | 13 | a0001c0001t0039g0230a0001c0001t0045g0066a0001c0001t0047g0074others(10): Show | 13 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181-1668G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792707 | ||||||
chr4:40792722
|
A | G | 1 | a0002c0002t0001g0262 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1181-1653A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792722 | ||||||
chr4:40792723
|
G | C | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1181-1652G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792723 | ||||||
chr4:40792731
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 220 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.1181-1644G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792731 | ||||||
chr4:40792763
|
A | AAAG | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 222 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.1181-1611_1181-160 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 40792763 | |||||
chr4:40792763
|
A | G | 2 | a0001c0001t0012g0330a0001c0001t0020g0331 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1181-1612A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792763 | ||||||
chr4:40793181
|
C | G | 1 | a0002c0002t0001g0299 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1181-1194C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793181 | ||||||
chr4:40793199
|
T | C | 1 | a0002c0002t0001g0301 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1181-1176T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793199 | ||||||
chr4:40793311
|
G | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-1064G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793311 | ||||||
chr4:40793415
|
C | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1181-960C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793415 | ||||||
chr4:40793441
|
C | CA | 14 | a0001c0001t0039g0230a0001c0001t0045g0066a0001c0001t0047g0074others(11): Show | 14 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1181-927dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 40793441 | |||||
chr4:40793523
|
G | A | 1 | a0002c0002t0001g0292 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1181-852G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793523 | ||||||
chr4:40793658
|
T | C | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1181-717T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793658 | ||||||
chr4:40793723
|
A | G | 11 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(8): Show | 11 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181-652A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793723 | ||||||
chr4:40793730
|
G | A | 3 | a0003c0003t0003g0217a0003c0003t0003g0226a0003c0022t0003g0353 | 3 | HG00140.hp1 HG03654.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1181-645G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793730 | ||||||
chr4:40793761
|
T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-614T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793761 | ||||||
chr4:40793791
|
T | C | 4 | a0001c0001t0002g0220a0001c0001t0010g0225a0001c0001t0019g0223others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-584T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793791 | ||||||
chr4:40793822
|
T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-553T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793822 | ||||||
chr4:40793836
|
A | G | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1181-539A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793836 | ||||||
chr4:40793841
|
T | C | 1 | a0003c0003t0006g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1181-534T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793841 | ||||||
chr4:40793868
|
A | C | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1181-507A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793868 | ||||||
chr4:40794290
|
A | C | 2 | a0001c0013t0002g0153a0005c0007t0028g0043 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1181-85A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40794290 | ||||||
chr4:40794346
|
A | G | 1 | a0002c0002t0005g0365 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1181-29A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40794346 | ||||||
chr4:40794542
|
C | T | 6 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+66C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794542 | ||||||
chr4:40794555
|
T | C | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+79T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794555 | ||||||
chr4:40794695
|
G | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0075others(25): Show | 30 | HG00558.hp1 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282+219G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794695 | ||||||
chr4:40794830
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 211 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.1282+354C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794830 | ||||||
chr4:40794876
|
G | C | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1282+400G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794876 | ||||||
chr4:40794990
|
C | T | 7 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(4): Show | 7 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282+514C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794990 | ||||||
chr4:40795235
|
A | G | 1 | a0001c0001t0007g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1282+759A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795235 | ||||||
chr4:40795350
|
C | T | 5 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282+874C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795350 | ||||||
chr4:40795478
|
T | A | 1 | a0003c0003t0011g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1282+1002T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795478 | ||||||
chr4:40795676
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 224 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+1200A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795676 | ||||||
chr4:40795733
|
C | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1282+1257C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795733 | ||||||
chr4:40795734
|
G | C | 1 | a0002c0002t0005g0323 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1282+1258G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795734 | ||||||
chr4:40795744
|
C | T | 1 | a0002c0002t0001g0297 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1282+1268C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795744 | ||||||
chr4:40795792
|
G | T | 5 | a0002c0002t0010g0096a0002c0002t0010g0119a0002c0002t0010g0135others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282+1316G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795792 | ||||||
chr4:40795806
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1282+1330C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795806 | ||||||
chr4:40795910
|
T | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 224 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+1434T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795910 | ||||||
chr4:40796095
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 224 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+1619T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796095 | ||||||
chr4:40796211
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 224 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1282+1735G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796211 | ||||||
chr4:40796244
|
C | T | 7 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(4): Show | 7 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282+1768C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796244 | ||||||
chr4:40796399
|
G | A | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+1923G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796399 | ||||||
chr4:40796490
|
A | C | 8 | a0001c0001t0009g0338a0001c0001t0009g0339a0001c0001t0009g0345others(5): Show | 8 | HG00735.hp2 HG01123.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282+2014A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796490 | ||||||
chr4:40796522
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282+2046C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796522 | ||||||
chr4:40796640
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1283-2147A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796640 | ||||||
chr4:40796680
|
C | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1283-2107C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796680 | ||||||
chr4:40796716
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1283-2071C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796716 | ||||||
chr4:40796718
|
G | A | 6 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1283-2069G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796718 | ||||||
chr4:40796791
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0058others(1): Show | 4 | HG03490.hp1 HG03704.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283-1996C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796791 | ||||||
chr4:40796988
|
G | A | 3 | a0001c0001t0018g0023a0001c0001t0018g0024a0003c0003t0014g0167 | 3 | NA18983.hp2 NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1283-1799G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796988 | ||||||
chr4:40796993
|
T | C | 1 | a0003c0003t0003g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1283-1794T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796993 | ||||||
chr4:40796999
|
G | A | 1 | a0002c0002t0001g0268 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1283-1788G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796999 | ||||||
chr4:40797006
|
A | G | 1 | a0010c0021t0002g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1283-1781A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797006 | ||||||
chr4:40797026
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1283-1761G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797026 | ||||||
chr4:40797082
|
C | G | 1 | a0001c0001t0002g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1283-1705C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797082 | ||||||
chr4:40797366
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1283-1421C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797366 | ||||||
chr4:40797514
|
C | T | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1283-1273C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797514 | ||||||
chr4:40797821
|
C | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 141 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1283-966C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797821 | ||||||
chr4:40797833
|
G | A | 1 | a0003c0003t0003g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1283-954G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797833 | ||||||
chr4:40797838
|
C | G | 26 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(23): Show | 26 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1283-949C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797838 | ||||||
chr4:40797896
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1283-891A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797896 | ||||||
chr4:40798060
|
T | C | 1 | a0012c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1283-727T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798060 | ||||||
chr4:40798107
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1283-680C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798107 | ||||||
chr4:40798112
|
G | T | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1283-675G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798112 | ||||||
chr4:40798128
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1283-659A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798128 | ||||||
chr4:40798130
|
A | G | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283-657A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798130 | ||||||
chr4:40798170
|
A | G | 12 | a0001c0001t0045g0066a0001c0001t0047g0074a0003c0003t0014g0167others(9): Show | 12 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1283-617A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798170 | ||||||
chr4:40798492
|
C | T | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1283-295C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798492 | ||||||
chr4:40799073
|
C | CT | 29 | a0001c0001t0001g0337a0002c0002t0001g0254a0002c0002t0001g0256others(26): Show | 29 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1400+198dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799073
|
C | CTTTTTG | 128 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 136 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1400+174_1400+175i others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799073
|
C | CTTTTTGT | 66 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(63): Show | 67 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1400+174_1400+175i others(9): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799073
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0002g0016 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1400+189_1400+198d others(12): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799073
|
CT | C | 8 | a0001c0001t0009g0339a0001c0001t0012g0344a0001c0001t0013g0334others(5): Show | 8 | HG00735.hp2 HG02055.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1400+198delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799073
|
CTT | C | 13 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(10): Show | 13 | HG01123.hp1 HG01192.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1400+197_1400+198d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799073
|
CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0001g0307 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1400+181_1400+198d others(20): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | |||||
chr4:40799074
|
T | TTTTTG | 55 | a0001c0001t0001g0088a0001c0001t0001g0137a0001c0001t0001g0200others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1400+174_1400+175i others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799074 | |||||
chr4:40799081
|
T | G | 2 | a0001c0001t0039g0230a0001c0013t0002g0153 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1400+177T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799081 | ||||||
chr4:40799084
|
T | G | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1400+180T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799084 | ||||||
chr4:40799087
|
T | G | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1400+183T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799087 | ||||||
chr4:40799088
|
T | G | 1 | a0006c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1400+184T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799088 | ||||||
chr4:40799090
|
T | G | 1 | a0005c0007t0048g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1400+186T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799090 | ||||||
chr4:40799102
|
T | A | 1 | a0002c0002t0004g0018 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1400+198T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799102 | ||||||
chr4:40799120
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0194others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1400+216C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799120 | ||||||
chr4:40799149
|
C | A | 8 | a0004c0004t0008g0068a0004c0004t0008g0069a0004c0004t0008g0070others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1400+245C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799149 | ||||||
chr4:40799242
|
C | CGG | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1400+339_1400+340i others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799242 | |||||
chr4:40799243
|
G | A | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1400+339G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799243 | ||||||
chr4:40799496
|
TA | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 160 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1400+607delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799496 | |||||
chr4:40799598
|
A | G | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1400+694A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799598 | ||||||
chr4:40799667
|
T | A | 2 | a0003c0003t0006g0165a0003c0003t0006g0370 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1400+763T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799667 | ||||||
chr4:40799848
|
C | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0137a0011c0019t0002g0104 | 3 | NA18948.hp2 NA19002.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1400+944C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799848 | ||||||
chr4:40799881
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+977G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799881 | ||||||
chr4:40800076
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1400+1172G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800076 | ||||||
chr4:40800080
|
T | C | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1400+1176T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800080 | ||||||
chr4:40800102
|
T | G | 16 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(13): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+1198T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800102 | ||||||
chr4:40800175
|
T | C | 44 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(41): Show | 44 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1400+1271T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800175 | ||||||
chr4:40800199
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1400+1295C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800199 | ||||||
chr4:40800486
|
C | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1400+1582C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800486 | ||||||
chr4:40800603
|
G | A | 5 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+1699G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800603 | ||||||
chr4:40800620
|
G | A | 18 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(15): Show | 18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1400+1716G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800620 | ||||||
chr4:40800889
|
T | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+1985T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800889 | ||||||
chr4:40800893
|
C | T | 26 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(23): Show | 26 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1400+1989C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800893 | ||||||
chr4:40801061
|
A | AAGGGAGG others(29): Show |
1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+2172_1400+217 others(40): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801061 | |||||
chr4:40801077
|
G | A | 5 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+2173G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801077 | ||||||
chr4:40801079
|
G | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 141 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1400+2175G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801079 | ||||||
chr4:40801081
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+2177G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801081 | ||||||
chr4:40801186
|
A | G | 16 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(13): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+2282A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801186 | ||||||
chr4:40801353
|
T | C | 16 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(13): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+2449T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801353 | ||||||
chr4:40801409
|
A | T | 8 | a0001c0001t0007g0241a0001c0001t0007g0242a0001c0001t0007g0245others(5): Show | 8 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1400+2505A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801409 | ||||||
chr4:40801611
|
T | G | 1 | a0002c0002t0001g0297 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1400+2707T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801611 | ||||||
chr4:40801623
|
C | A | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1400+2719C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801623 | ||||||
chr4:40801723
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1400+2819C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801723 | ||||||
chr4:40801725
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 285 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1400+2821T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801725 | ||||||
chr4:40801758
|
G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1400+2854G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801758 | ||||||
chr4:40801759
|
T | TGTG | 6 | a0001c0001t0001g0011a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 6 | HG01891.hp2 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1400+2865_1400+286 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801759 | |||||
chr4:40801795
|
G | A | 1 | a0006c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1400+2891G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801795 | ||||||
chr4:40801816
|
T | C | 16 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(13): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+2912T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801816 | ||||||
chr4:40801901
|
C | CA | 7 | a0001c0001t0002g0196a0001c0013t0002g0153a0002c0002t0001g0260others(4): Show | 7 | HG00621.hp2 HG02027.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1400+3015dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | |||||
chr4:40801901
|
C | CAA | 19 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(16): Show | 19 | HG00735.hp2 HG01069.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1400+3014_1400+301 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | |||||
chr4:40801901
|
C | CAAA | 22 | a0001c0001t0012g0330a0003c0003t0003g0237a0003c0003t0006g0049others(19): Show | 22 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1400+3013_1400+301 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | |||||
chr4:40801901
|
C | CAAAA | 17 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(14): Show | 17 | HG00438.hp1 HG00733.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1400+3012_1400+301 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | |||||
chr4:40801901
|
CAAAAAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 157 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1400+3010_1400+301 others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | |||||
chr4:40801942
|
G | A | 1 | a0006c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1400+3038G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801942 | ||||||
chr4:40801962
|
T | G | 28 | a0001c0001t0001g0229a0001c0001t0002g0186a0001c0001t0002g0187others(25): Show | 28 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1400+3058T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801962 | ||||||
chr4:40802117
|
A | G | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1400+3213A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802117 | ||||||
chr4:40802338
|
AT | A | 61 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1400+3443delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802338 | |||||
chr4:40802340
|
T | A | 3 | a0001c0001t0018g0023a0001c0001t0018g0024a0001c0001t0039g0230 | 3 | HG02976.hp2 NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1400+3436T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802340 | ||||||
chr4:40802520
|
A | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 145 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1400+3616A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802520 | ||||||
chr4:40802575
|
C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+3671C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802575 | ||||||
chr4:40802631
|
A | ATGTT | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1400+3737_1400+374 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802631 | |||||
chr4:40802641
|
G | GTTTGT | 5 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+3740_1400+374 others(9): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802641 | |||||
chr4:40802645
|
T | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+3741T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802645 | ||||||
chr4:40802691
|
A | T | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1400+3787A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802691 | ||||||
chr4:40802738
|
A | G | 4 | a0003c0003t0006g0049a0003c0003t0006g0059a0003c0003t0006g0060others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1400+3834A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802738 | ||||||
chr4:40802783
|
C | CT | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1400+3896dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802783 | |||||
chr4:40802783
|
CT | C | 48 | a0001c0001t0001g0201a0001c0001t0009g0193a0001c0001t0009g0335others(45): Show | 48 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1400+3896delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802783 | |||||
chr4:40802793
|
T | G | 2 | a0003c0003t0014g0167a0006c0006t0034g0363 | 2 | NA18906.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1400+3889T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802793 | ||||||
chr4:40802827
|
T | C | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1400+3923T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802827 | ||||||
chr4:40802841
|
A | G | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1400+3937A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802841 | ||||||
chr4:40802994
|
T | A | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1401-4067T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802994 | ||||||
chr4:40803007
|
A | G | 1 | a0002c0002t0001g0285 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1401-4054A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803007 | ||||||
chr4:40803032
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 294 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.1401-4029T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803032 | ||||||
chr4:40803117
|
C | T | 1 | a0003c0003t0016g0361 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1401-3944C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803117 | ||||||
chr4:40803164
|
A | G | 55 | a0001c0001t0045g0066a0001c0001t0047g0074a0003c0003t0003g0028others(52): Show | 55 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1401-3897A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803164 | ||||||
chr4:40803235
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 162 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1401-3826C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803235 | ||||||
chr4:40803402
|
G | A | 19 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(16): Show | 19 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1401-3659G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803402 | ||||||
chr4:40803422
|
A | G | 7 | a0003c0003t0011g0159a0003c0003t0011g0162a0003c0003t0011g0163others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-3639A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803422 | ||||||
chr4:40803472
|
C | T | 1 | a0003c0003t0044g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1401-3589C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803472 | ||||||
chr4:40803525
|
C | A | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1401-3536C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803525 | ||||||
chr4:40803547
|
G | T | 10 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(7): Show | 10 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1401-3514G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803547 | ||||||
chr4:40803603
|
A | G | 44 | a0003c0003t0003g0028a0003c0003t0003g0029a0003c0003t0003g0030others(41): Show | 44 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1401-3458A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803603 | ||||||
chr4:40803705
|
C | T | 7 | a0001c0001t0002g0184a0001c0001t0002g0190a0001c0001t0002g0191others(4): Show | 7 | HG01070.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-3356C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803705 | ||||||
chr4:40803742
|
G | C | 1 | a0007c0005t0001g0294 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1401-3319G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803742 | ||||||
chr4:40803747
|
G | C | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1401-3314G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803747 | ||||||
chr4:40803775
|
G | T | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1401-3286G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803775 | ||||||
chr4:40803949
|
C | G | 2 | a0001c0001t0018g0023a0001c0001t0018g0024 | 2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1401-3112C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803949 | ||||||
chr4:40803993
|
G | A | 4 | a0002c0002t0010g0119a0002c0002t0010g0135a0002c0002t0010g0144others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401-3068G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803993 | ||||||
chr4:40804137
|
G | A | 1 | a0001c0001t0007g0242 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1401-2924G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804137 | ||||||
chr4:40804208
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1401-2853G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804208 | ||||||
chr4:40804268
|
C | T | 1 | a0003c0003t0031g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1401-2793C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804268 | ||||||
chr4:40804313
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0121a0001c0001t0001g0130others(3): Show | 7 | HG00558.hp1 NA18946.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-2748G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804313 | ||||||
chr4:40804387
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1401-2674C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804387 | ||||||
chr4:40804438
|
C | CA | 13 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0001g0133others(10): Show | 13 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1401-2608dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40804438 | |||||
chr4:40804438
|
CA | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0041g0248others(4): Show | 7 | HG01070.hp2 HG01168.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-2608delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40804438 | |||||
chr4:40804539
|
A | G | 1 | a0001c0001t0009g0339 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1401-2522A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804539 | ||||||
chr4:40804670
|
A | C | 1 | a0001c0001t0007g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1401-2391A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804670 | ||||||
chr4:40804841
|
T | G | 16 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(13): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1401-2220T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804841 | ||||||
chr4:40805001
|
A | G | 9 | a0001c0001t0004g0244a0001c0001t0007g0241a0001c0001t0007g0242others(6): Show | 9 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1401-2060A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805001 | ||||||
chr4:40805224
|
T | A | 5 | a0003c0003t0015g0158a0003c0003t0015g0240a0003c0003t0016g0239others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1401-1837T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805224 | ||||||
chr4:40805282
|
G | A | 7 | a0001c0001t0002g0184a0001c0001t0002g0190a0001c0001t0002g0191others(4): Show | 7 | HG01070.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-1779G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805282 | ||||||
chr4:40805401
|
G | A | 1 | a0005c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1401-1660G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805401 | ||||||
chr4:40806120
|
G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1401-941G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806120 | ||||||
chr4:40806148
|
C | T | 1 | a0006c0006t0034g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1401-913C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806148 | ||||||
chr4:40806247
|
G | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1401-814G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806247 | ||||||
chr4:40806275
|
G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1401-786G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806275 | ||||||
chr4:40806367
|
A | G | 2 | a0001c0001t0004g0244a0001c0001t0007g0243 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1401-694A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806367 | ||||||
chr4:40806707
|
A | G | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1401-354A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806707 | ||||||
chr4:40806749
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1401-312A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806749 | ||||||
chr4:40806761
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(279): Show | 291 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.1401-300G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806761 | ||||||
chr4:40806762
|
C | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1401-299C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806762 | ||||||
chr4:40806763
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1401-298C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806763 | ||||||
chr4:40806765
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1401-296T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806765 | ||||||
chr4:40806861
|
A | G | 1 | a0003c0003t0006g0370 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1401-200A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806861 | ||||||
chr4:40807190
|
GA | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 140 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1524+14delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40807190 | |||||
chr4:40807211
|
T | A | 1 | a0001c0001t0001g0094 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1524+27T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807211 | ||||||
chr4:40807287
|
T | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1524+103T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807287 | ||||||
chr4:40807296
|
A | C | 1 | a0007c0005t0001g0282 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1524+112A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807296 | ||||||
chr4:40807350
|
C | CT | 22 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(19): Show | 22 | HG00735.hp1 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+182dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40807350 | |||||
chr4:40807350
|
CT | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 210 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1524+182delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40807350 | |||||
chr4:40807372
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 285 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1524+188A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807372 | ||||||
chr4:40807434
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1524+250C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807434 | ||||||
chr4:40807628
|
G | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 108 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1524+444G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807628 | ||||||
chr4:40807641
|
C | T | 2 | a0001c0001t0012g0330a0001c0001t0020g0331 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1524+457C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807641 | ||||||
chr4:40807669
|
C | T | 3 | a0001c0001t0018g0023a0001c0001t0018g0024a0001c0001t0039g0230 | 3 | HG02976.hp2 NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1524+485C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807669 | ||||||
chr4:40807678
|
C | G | 10 | a0001c0001t0045g0066a0001c0001t0047g0074a0004c0004t0008g0068others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+494C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807678 | ||||||
chr4:40807746
|
T | C | 1 | a0002c0002t0001g0297 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1525-561T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807746 | ||||||
chr4:40807779
|
A | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1525-528A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807779 | ||||||
chr4:40807991
|
G | A | 16 | a0001c0001t0009g0193a0001c0001t0009g0335a0001c0001t0009g0336others(13): Show | 16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1525-316G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807991 | ||||||
chr4:40808029
|
C | CA | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 152 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.1525-254dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808029 | |||||
chr4:40808029
|
C | CAA | 32 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0053others(29): Show | 33 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1525-255_1525-254d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808029 | |||||
chr4:40808029
|
CA | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0200others(48): Show | 51 | HG00621.hp2 HG00735.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1525-254delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808029 | |||||
chr4:40808109
|
GT | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1525-188delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808109 | |||||
chr4:40808116
|
T | G | 1 | a0001c0001t0001g0337 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1525-191T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40808116 |