geneid | 79634 |
---|---|
ensemblid | ENSG00000144306.15 |
hgncid | 30382 |
symbol | SCRN3 |
name | secernin 3 |
refseq_nuc | NM_024583.5 |
refseq_prot | NP_078859.2 |
ensembl_nuc | ENST00000272732.11 |
ensembl_prot | ENSP00000272732.6 |
mane_status | MANE Select |
chr | chr2 |
start | 174395730 |
end | 174429575 |
strand | + |
ver | v1.2 |
region | chr2:174395730-174429575 |
region5000 | chr2:174390730-174434575 |
regionname0 | SCRN3_chr2_174395730_174429575 |
regionname5000 | SCRN3_chr2_174390730_174434575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/1 | 0 | 88 | 5 | 15 | 45 | 7 | 15 | 38 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001 | 1/0 | 424 | 238 | 83 | 39 | 80 | 7 | 28 | 65 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0002 | 0/0 | 424 | 29 | 1 | 21 | 0 | 4 | 3 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0003 | 0/0 | 424 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0004 | 0/0 | 424 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0005 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0006 | 0/0 | 424 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0007 | 0/0 | 424 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0008 | 0/0 | 424 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1275 | 234 | 79 | 39 | 80 | 7 | 28 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0002 | 0/0 | 1262 | 72 | 4 | 10 | 45 | 5 | 8 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0003 | 0/0 | 1275 | 29 | 1 | 21 | 0 | 4 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0004 | 0/1 | 1262 | 15 | 0 | 5 | 0 | 2 | 7 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0005 | 0/0 | 1275 | 4 | 4 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0006 | 0/0 | 1275 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0007 | 0/0 | 1275 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0008 | 0/0 | 1262 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0009 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0010 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0011 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
c0012 | 0/0 | 1275 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
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 | 1/0 | 1778 | 230 | 51 | 60 | 77 | 11 | 30 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0002 | 0/1 | 1778 | 70 | 4 | 9 | 45 | 2 | 9 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0003 | 0/0 | 1778 | 18 | 17 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0004 | 0/0 | 1778 | 17 | 1 | 6 | 0 | 4 | 6 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0005 | 0/0 | 1778 | 8 | 7 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0006 | 0/0 | 1778 | 5 | 5 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0007 | 0/0 | 1778 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0008 | 0/0 | 1778 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0009 | 0/0 | 1778 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0010 | 0/0 | 1778 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0011 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0012 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0013 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0014 | 0/0 | 1778 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0015 | 0/0 | 1778 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0016 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0017 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
t0018 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
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 | 14 | 0 | 1 | 8 | 1 | 4 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0003 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0004 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0006 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0008 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0011 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0018 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0002 | 0/0 | 1262 | 72 | 4 | 10 | 45 | 5 | 8 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0000c0004 | 0/1 | 1262 | 15 | 0 | 5 | 0 | 2 | 7 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0000c0008 | 0/0 | 1262 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001 | 1/0 | 1275 | 234 | 79 | 39 | 80 | 7 | 28 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0005 | 0/0 | 1275 | 4 | 4 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0002c0003 | 0/0 | 1275 | 29 | 1 | 21 | 0 | 4 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0003c0006 | 0/0 | 1275 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0004c0007 | 0/0 | 1275 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0005c0009 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0006c0011 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0007c0010 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0008c0012 | 0/0 | 1275 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0002t0002 | 0/0 | 3039 | 54 | 3 | 4 | 45 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0000c0002t0004 | 0/0 | 3039 | 17 | 1 | 6 | 0 | 4 | 6 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0000c0002t0012 | 0/0 | 3039 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0000c0004t0002 | 0/1 | 3039 | 15 | 0 | 5 | 0 | 2 | 7 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0000c0008t0002 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0001 | 1/0 | 3052 | 192 | 45 | 38 | 76 | 7 | 25 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0003 | 0/0 | 3052 | 18 | 17 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0005 | 0/0 | 3052 | 8 | 7 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0006 | 0/0 | 3052 | 5 | 5 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0007 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0008 | 0/0 | 3052 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0009 | 0/0 | 3052 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0011 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0013 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0016 | 0/0 | 3052 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0017 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0001t0018 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0001c0005t0001 | 0/0 | 3052 | 4 | 4 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0002c0003t0001 | 0/0 | 3052 | 27 | 1 | 19 | 0 | 4 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0002c0003t0014 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0002c0003t0015 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0003c0006t0001 | 0/0 | 3052 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0004c0007t0010 | 0/0 | 3052 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0005c0009t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0006c0011t0001 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0007c0010t0001 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
a0008c0012t0001 | 0/0 | 3052 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | copy fasta | chr2 | 174390730 | 174434575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0002t0002g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0006 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0002t0012g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0011 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0000c0008t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0001 | 0/0 | 12 | 0 | 1 | 7 | 1 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0018 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0016g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0017g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0001t0018g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0004 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0014g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0002c0003t0015g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0003c0006t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0004c0007t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0004c0007t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0005c0009t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0006c0011t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0007c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
a0008c0012t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00323 | hp2 | a0000 | c0002 | t0004 | g0063 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00558 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00639 | hp2 | a0000 | c0002 | t0004 | g0006 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00642 | hp2 | a0000 | c0002 | t0002 | g0066 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00673 | hp1 | a0000 | c0002 | t0002 | g0023 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00733 | hp2 | a0000 | c0004 | t0002 | g0011 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00735 | hp1 | a0000 | c0004 | t0002 | g0075 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00738 | hp1 | a0003 | c0006 | t0001 | g0022 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00738 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00741 | hp1 | a0000 | c0004 | t0002 | g0011 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG00741 | hp2 | a0002 | c0003 | t0014 | g0136 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0140 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0138 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01070 | hp2 | a0000 | c0004 | t0002 | g0076 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0035 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01081 | hp1 | a0000 | c0002 | t0002 | g0010 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0139 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01109 | hp1 | a0002 | c0003 | t0015 | g0124 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01109 | hp2 | a0000 | c0002 | t0004 | g0024 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0134 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0130 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0141 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0125 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01256 | hp1 | a0000 | c0002 | t0004 | g0006 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0127 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01258 | hp1 | a0000 | c0002 | t0004 | g0006 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01358 | hp2 | a0000 | c0002 | t0002 | g0010 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01361 | hp2 | a0000 | c0002 | t0002 | g0067 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01433 | hp2 | a0000 | c0002 | t0004 | g0060 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01496 | hp1 | a0000 | c0004 | t0002 | g0079 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01496 | hp2 | a0003 | c0006 | t0001 | g0022 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01515 | hp1 | a0002 | c0003 | t0001 | g0128 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01515 | hp2 | a0000 | c0002 | t0004 | g0062 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01516 | hp1 | a0000 | c0004 | t0002 | g0078 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0035 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01517 | hp1 | a0000 | c0004 | t0002 | g0077 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0129 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01891 | hp2 | a0001 | c0005 | t0001 | g0158 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01952 | hp2 | a0006 | c0011 | t0001 | g0178 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0214 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01978 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01981 | hp1 | a0002 | c0003 | t0001 | g0126 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02015 | hp1 | a0000 | c0002 | t0002 | g0017 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02027 | hp1 | a0000 | c0002 | t0002 | g0227 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02027 | hp2 | a0000 | c0002 | t0002 | g0068 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02080 | hp2 | a0000 | c0002 | t0002 | g0009 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02300 | hp1 | a0000 | c0002 | t0004 | g0065 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02523 | hp1 | a0000 | c0002 | t0002 | g0056 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02572 | hp1 | a0000 | c0002 | t0004 | g0086 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02572 | hp2 | a0000 | c0002 | t0002 | g0224 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02602 | hp1 | a0001 | c0001 | t0016 | g0190 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0019 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02683 | hp2 | a0000 | c0004 | t0002 | g0074 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02698 | hp1 | a0000 | c0002 | t0004 | g0061 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0232 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02735 | hp1 | a0000 | c0004 | t0002 | g0081 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02738 | hp1 | a0000 | c0004 | t0002 | g0071 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02976 | hp2 | a0001 | c0001 | t0018 | g0083 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03017 | hp2 | a0000 | c0002 | t0004 | g0006 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0157 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0085 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03209 | hp2 | a0007 | c0010 | t0001 | g0148 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03239 | hp2 | a0000 | c0002 | t0002 | g0010 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03490 | hp2 | a0000 | c0002 | t0004 | g0006 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03491 | hp2 | a0000 | c0004 | t0002 | g0025 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03492 | hp1 | a0000 | c0004 | t0002 | g0025 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03492 | hp2 | a0000 | c0002 | t0004 | g0006 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0159 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03688 | hp1 | a0002 | c0003 | t0001 | g0019 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0189 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03710 | hp1 | a0003 | c0006 | t0001 | g0022 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03710 | hp2 | a0002 | c0003 | t0001 | g0135 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03831 | hp2 | a0000 | c0004 | t0002 | g0073 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03927 | hp1 | a0008 | c0012 | t0001 | g0201 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04184 | hp1 | a0000 | c0002 | t0004 | g0069 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04199 | hp2 | a0000 | c0002 | t0004 | g0024 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04204 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG04228 | hp2 | a0000 | c0002 | t0002 | g0226 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18522 | hp2 | a0000 | c0002 | t0002 | g0059 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18939 | hp2 | a0000 | c0002 | t0002 | g0056 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18945 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18946 | hp2 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18947 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18948 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18954 | hp2 | a0000 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18963 | hp1 | a0000 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18964 | hp1 | a0004 | c0007 | t0010 | g0110 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18964 | hp2 | a0000 | c0002 | t0002 | g0221 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18965 | hp2 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18968 | hp1 | a0000 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18972 | hp1 | a0000 | c0002 | t0002 | g0054 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18974 | hp2 | a0000 | c0002 | t0002 | g0053 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18977 | hp2 | a0000 | c0002 | t0002 | g0220 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18981 | hp2 | a0000 | c0002 | t0002 | g0218 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18983 | hp1 | a0000 | c0002 | t0002 | g0055 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18986 | hp2 | a0000 | c0002 | t0002 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18991 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18993 | hp2 | a0000 | c0002 | t0002 | g0055 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18994 | hp2 | a0001 | c0001 | t0017 | g0015 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18995 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18998 | hp2 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19000 | hp1 | a0000 | c0002 | t0002 | g0217 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19003 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19006 | hp1 | a0000 | c0002 | t0002 | g0023 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19007 | hp2 | a0000 | c0002 | t0002 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19010 | hp1 | a0000 | c0002 | t0002 | g0225 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19030 | hp1 | a0000 | c0008 | t0002 | g0146 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19043 | hp1 | a0000 | c0002 | t0002 | g0215 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19056 | hp2 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19057 | hp1 | a0000 | c0002 | t0002 | g0017 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19060 | hp1 | a0005 | c0009 | t0001 | g0175 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19062 | hp1 | a0000 | c0002 | t0002 | g0222 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19064 | hp1 | a0000 | c0002 | t0002 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19065 | hp2 | a0000 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19066 | hp2 | a0000 | c0002 | t0002 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19076 | hp2 | a0000 | c0002 | t0002 | g0228 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19080 | hp1 | a0000 | c0002 | t0002 | g0216 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19089 | hp1 | a0000 | c0002 | t0002 | g0023 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19089 | hp2 | a0004 | c0007 | t0010 | g0109 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19090 | hp1 | a0000 | c0002 | t0002 | g0054 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19090 | hp2 | a0000 | c0002 | t0002 | g0017 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19091 | hp2 | a0000 | c0002 | t0002 | g0053 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ASW | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | ASW | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0137 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20752 | hp2 | a0000 | c0002 | t0004 | g0070 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20805 | hp1 | a0000 | c0002 | t0012 | g0010 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20805 | hp2 | a0000 | c0002 | t0004 | g0064 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20905 | hp1 | a0000 | c0004 | t0002 | g0011 | SAS | GIH | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0131 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18955 | hp1 | a0000 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0230 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
homoSapiens_chm13v2 | hp1 | a0000 | c0004 | t0002 | g0011 | REF | REF | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174398335
|
G | A | 1 | a0002 | 29 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
missense_variant | MODERATE | c.52G>A | p.Asp18Asn | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/8 | 149/3052 | 52/1275 | 18/424 | chr2 | 174398335 | ||
chr2:174399983
|
C | T | 1 | a0008 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.221C>T | p.Ala74Val | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/8 | 318/3052 | 221/1275 | 74/424 | chr2 | 174399983 | ||
chr2:174401184
|
T | C | 1 | a0000 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.536T>C | p.Val179Ala | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/8 | 633/3052 | 536/1275 | 179/424 | chr2 | 174401184 | ||
chr2:174404132
|
T | G | 1 | a0005 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.571T>G | p.Ser191Ala | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/8 | 668/3052 | 571/1275 | 191/424 | chr2 | 174404132 | ||
chr2:174422999
|
C | G | 1 | a0006 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.869C>G | p.Ser290Cys | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/8 | 966/3052 | 869/1275 | 290/424 | chr2 | 174422999 | ||
chr2:174424531
|
G | T | 1 | a0003 | 3 | HG00738.hp1 HG01496.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.974G>T | p.Ser325Ile | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/8 | 1071/3052 | 974/1275 | 325/424 | chr2 | 174424531 | ||
chr2:174427785
|
C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1165C>T | p.Leu389Phe | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1262/3052 | 1165/1275 | 389/424 | chr2 | 174427785 | ||
chr2:174427852
|
TTCAAATT others(6): Show |
T | 1 | a0000 | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
frameshift_variant | HIGH | c.1251_1263delTTTATC others(7): Show |
p.Asn417fs | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1348/3052 | 1251/1275 | 417/424 | INFO_REALIGN_3_PRIME | chr2 | 174427852 | |
chr2:174427882
|
A | T | 1 | a0004 | 2 | NA18964.hp1 NA19089.hp2 |
missense_variant | MODERATE | c.1262A>T | p.Lys421Ile | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1359/3052 | 1262/1275 | 421/424 | chr2 | 174427882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174398334
|
C | T | 1 | a0001c0005 | 4 | HG01891.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.51C>T | p.Val17Val | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/8 | 148/3052 | 51/1275 | 17/424 | chr2 | 174398334 | ||
chr2:174424586
|
T | C | 1 | a0000c0004 | 15 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(12): Show |
synonymous_variant | LOW | c.1029T>C | p.Pro343Pro | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/8 | 1126/3052 | 1029/1275 | 343/424 | chr2 | 174424586 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174395733
|
A | T | 2 | a0001c0001t0006a0001c0001t0018 | 6 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-94A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/8 | 2551 | chr2 | 174395733 | |||||
chr2:174428105
|
G | A | 1 | a0001c0001t0011 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*210G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 210 | chr2 | 174428105 | |||||
chr2:174428111
|
T | C | 2 | a0001c0001t0003a0001c0001t0007 | 20 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*216T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 216 | chr2 | 174428111 | |||||
chr2:174428160
|
G | C | 5 | a0000c0002t0002a0000c0002t0004a0000c0002t0012others(2): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*265G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 265 | chr2 | 174428160 | |||||
chr2:174428196
|
A | G | 1 | a0004c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*301A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 301 | chr2 | 174428196 | |||||
chr2:174428220
|
G | T | 1 | a0001c0001t0009 | 2 | HG03704.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*325G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 325 | chr2 | 174428220 | |||||
chr2:174428351
|
C | A | 2 | a0001c0001t0005a0001c0001t0013 | 9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*456C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 456 | chr2 | 174428351 | |||||
chr2:174428589
|
G | T | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 694 | chr2 | 174428589 | |||||
chr2:174428620
|
G | A | 1 | a0002c0003t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 725 | chr2 | 174428620 | |||||
chr2:174428761
|
A | G | 1 | a0001c0001t0008 | 2 | NA18979.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*866A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 866 | chr2 | 174428761 | |||||
chr2:174428768
|
T | C | 1 | a0002c0003t0015 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 873 | chr2 | 174428768 | |||||
chr2:174428910
|
C | T | 5 | a0000c0002t0002a0000c0002t0004a0000c0002t0012others(2): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1015C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1015 | chr2 | 174428910 | |||||
chr2:174428968
|
A | C | 1 | a0004c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1073 | chr2 | 174428968 | |||||
chr2:174429018
|
A | C | 1 | a0001c0001t0018 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1123A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1123 | chr2 | 174429018 | |||||
chr2:174429081
|
A | G | 1 | a0004c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1186A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1186 | chr2 | 174429081 | |||||
chr2:174429294
|
C | T | 1 | a0001c0001t0007 | 2 | HG02109.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1399C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1399 | chr2 | 174429294 | |||||
chr2:174429319
|
C | T | 1 | a0004c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1424C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1424 | chr2 | 174429319 | |||||
chr2:174429340
|
C | T | 1 | a0000c0002t0012 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1445C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1445 | chr2 | 174429340 | |||||
chr2:174429351
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1456 | chr2 | 174429351 | |||||
chr2:174429476
|
G | T | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1581G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1581 | chr2 | 174429476 | |||||
chr2:174429525
|
A | C | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1630A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1630 | chr2 | 174429525 | |||||
chr2:174429526
|
A | G | 4 | a0000c0002t0002a0000c0002t0012a0000c0004t0002others(1): Show | 71 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1631A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1631 | chr2 | 174429526 | |||||
chr2:174429529
|
C | T | 4 | a0000c0002t0002a0000c0002t0012a0000c0004t0002others(1): Show | 71 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1634C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1634 | chr2 | 174429529 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:174396181
|
A | T | 29 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0016others(26): Show | 54 | HG00558.hp1 HG00673.hp1 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+364A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396181 | ||||||
chr2:174396349
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10+532G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396349 | ||||||
chr2:174396420
|
T | C | 52 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(49): Show | 90 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.-10+603T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396420 | ||||||
chr2:174396569
|
GGTGGATC others(4): Show |
G | 1 | a0000c0002t0002g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+754_-10+764del others(11): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174396569 | |||||
chr2:174396690
|
C | G | 1 | a0002c0003t0001g0214 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-10+873C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396690 | ||||||
chr2:174396697
|
T | C | 39 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(36): Show | 73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10+880T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396697 | ||||||
chr2:174396715
|
T | C | 33 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(30): Show | 42 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10+898T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396715 | ||||||
chr2:174396721
|
G | C | 39 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(36): Show | 73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10+904G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396721 | ||||||
chr2:174396734
|
G | T | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-10+917G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396734 | ||||||
chr2:174396796
|
C | CA | 8 | a0000c0004t0002g0025a0000c0004t0002g0071a0001c0001t0001g0031others(5): Show | 11 | HG02165.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+991dupA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174396796 | |||||
chr2:174396808
|
A | AAAAAAC | 35 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(32): Show | 69 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-10+991_-10+992ins others(6): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396808 | ||||||
chr2:174396809
|
C | A | 41 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(38): Show | 75 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10+992C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396809 | ||||||
chr2:174396849
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-10+1032C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396849 | ||||||
chr2:174397002
|
G | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1185G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397002 | ||||||
chr2:174397026
|
A | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1209A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397026 | ||||||
chr2:174397204
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-9-1071T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397204 | ||||||
chr2:174397249
|
C | T | 1 | a0001c0001t0006g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9-1026C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397249 | ||||||
chr2:174397282
|
C | T | 46 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(43): Show | 81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-993C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397282 | ||||||
chr2:174397345
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9-930G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397345 | ||||||
chr2:174397422
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9-853G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397422 | ||||||
chr2:174397434
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-9-841G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397434 | ||||||
chr2:174397457
|
C | A | 1 | a0001c0001t0018g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-818C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397457 | ||||||
chr2:174397560
|
A | G | 2 | a0000c0002t0002g0016a0000c0002t0002g0218 | 5 | NA18954.hp2 NA18963.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-715A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397560 | ||||||
chr2:174397714
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-9-561G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397714 | ||||||
chr2:174397900
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-9-375T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397900 | ||||||
chr2:174397950
|
G | A | 44 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(41): Show | 79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9-325G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397950 | ||||||
chr2:174398036
|
G | A | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-239G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174398036 | ||||||
chr2:174398072
|
AAGCCCTG others(18): Show |
A | 12 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(9): Show | 16 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-198_-9-174delCT others(23): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174398072 | |||||
chr2:174398239
|
G | GT | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-34dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174398239 | |||||
chr2:174398242
|
C | T | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9-33C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174398242 | ||||||
chr2:174398490
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.159+48A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398490 | ||||||
chr2:174398607
|
C | T | 39 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(36): Show | 73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.159+165C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398607 | ||||||
chr2:174398753
|
C | G | 232 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(229): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.159+311C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398753 | ||||||
chr2:174398794
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+352T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398794 | ||||||
chr2:174398903
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.159+461G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398903 | ||||||
chr2:174398940
|
A | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.159+498A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398940 | ||||||
chr2:174399004
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.159+562C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174399004 | ||||||
chr2:174399590
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.160-332A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174399590 | ||||||
chr2:174399899
|
C | CT | 33 | a0000c0002t0004g0086a0000c0004t0002g0011a0000c0004t0002g0071others(30): Show | 43 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.160-5dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | |||||
chr2:174399899
|
C | CTT | 31 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027others(28): Show | 40 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.160-6_160-5dupTT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | |||||
chr2:174399899
|
CT | C | 25 | a0000c0004t0002g0073a0000c0004t0002g0074a0001c0001t0001g0034others(22): Show | 29 | HG01109.hp1 HG01123.hp1 HG01192.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.160-5delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | |||||
chr2:174399899
|
CTTTT | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.160-8_160-5delTTTT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | |||||
chr2:174400217
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+114G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400217 | ||||||
chr2:174400329
|
C | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+226C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400329 | ||||||
chr2:174400355
|
T | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.341+252T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400355 | ||||||
chr2:174400463
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 130 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.341+360A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400463 | ||||||
chr2:174400470
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.341+367A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400470 | ||||||
chr2:174400471
|
T | A | 31 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0016others(28): Show | 64 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.341+368T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400471 | ||||||
chr2:174400486
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.341+383C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400486 | ||||||
chr2:174400681
|
A | G | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.342-309A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400681 | ||||||
chr2:174400718
|
A | G | 1 | a0001c0001t0001g0030 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.342-272A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400718 | ||||||
chr2:174400817
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0174 | 4 | HG01192.hp2 HG01981.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-173T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400817 | ||||||
chr2:174400884
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0174 | 4 | HG01192.hp2 HG01981.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-106T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400884 | ||||||
chr2:174400886
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.342-104G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400886 | ||||||
chr2:174400938
|
A | G | 46 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(43): Show | 81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.342-52A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400938 | ||||||
chr2:174400974
|
T | C | 1 | a0000c0002t0004g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.342-16T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400974 | ||||||
chr2:174401332
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.541+143A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401332 | ||||||
chr2:174401489
|
A | AT | 4 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0001g0132others(1): Show | 5 | HG02280.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+303dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174401489 | |||||
chr2:174401531
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.541+342T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401531 | ||||||
chr2:174401562
|
G | A | 51 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(48): Show | 68 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.541+373G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401562 | ||||||
chr2:174401631
|
A | C | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.541+442A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401631 | ||||||
chr2:174401796
|
C | A | 10 | a0001c0001t0003g0020a0001c0001t0003g0039a0001c0001t0003g0040others(7): Show | 15 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.541+607C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401796 | ||||||
chr2:174401860
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.541+671G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401860 | ||||||
chr2:174402076
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541+887A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402076 | ||||||
chr2:174402127
|
A | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.541+938A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402127 | ||||||
chr2:174402144
|
G | C | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.541+955G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402144 | ||||||
chr2:174402159
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.541+970T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402159 | ||||||
chr2:174402309
|
A | G | 1 | a0000c0004t0002g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.541+1120A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402309 | ||||||
chr2:174402323
|
T | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.541+1134T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402323 | ||||||
chr2:174402340
|
T | C | 16 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0066others(13): Show | 26 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.541+1151T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402340 | ||||||
chr2:174402390
|
T | G | 2 | a0001c0001t0001g0042a0005c0009t0001g0175 | 3 | NA18952.hp2 NA18993.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.541+1201T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402390 | ||||||
chr2:174402666
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.542-1437G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402666 | ||||||
chr2:174402717
|
G | A | 1 | a0001c0001t0006g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-1386G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402717 | ||||||
chr2:174402821
|
A | AT | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-1277dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174402821 | |||||
chr2:174403084
|
G | GT | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 128 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.542-1018dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403084 | |||||
chr2:174403085
|
T | TAA | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-1006_542-1005d others(4): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403085 | |||||
chr2:174403085
|
TA | T | 37 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(34): Show | 71 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.542-1005delA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403085 | |||||
chr2:174403086
|
A | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0173a0001c0001t0001g0202 | 4 | HG00280.hp2 HG02698.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-1017A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403086 | ||||||
chr2:174403138
|
C | T | 26 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(23): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.542-965C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403138 | ||||||
chr2:174403148
|
G | T | 2 | a0000c0004t0002g0071a0000c0004t0002g0081 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.542-955G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403148 | ||||||
chr2:174403315
|
A | C | 1 | a0008c0012t0001g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.542-788A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403315 | ||||||
chr2:174403527
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-576C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403527 | ||||||
chr2:174403528
|
CAATAAA | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-569_542-564del others(6): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403528 | |||||
chr2:174403569
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0204 | 2 | NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.542-534T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403569 | ||||||
chr2:174403606
|
C | T | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.542-497C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403606 | ||||||
chr2:174403716
|
G | A | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.542-387G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403716 | ||||||
chr2:174403743
|
G | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-360G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403743 | ||||||
chr2:174403882
|
AT | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-214delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403882 | |||||
chr2:174403976
|
C | G | 1 | a0001c0001t0001g0029 | 2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.542-127C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403976 | ||||||
chr2:174404035
|
A | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-68A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174404035 | ||||||
chr2:174404329
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.754+14A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404329 | ||||||
chr2:174404458
|
A | T | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+143A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404458 | ||||||
chr2:174404563
|
G | A | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+248G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404563 | ||||||
chr2:174404590
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.754+275A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404590 | ||||||
chr2:174404608
|
C | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+293C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404608 | ||||||
chr2:174404725
|
C | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+410C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404725 | ||||||
chr2:174404919
|
C | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+604C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404919 | ||||||
chr2:174404919
|
C | G | 5 | a0001c0001t0001g0199a0001c0005t0001g0157a0001c0005t0001g0158others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+604C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404919 | ||||||
chr2:174404941
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+626G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404941 | ||||||
chr2:174405015
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+700C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405015 | ||||||
chr2:174405018
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.754+703T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405018 | ||||||
chr2:174405026
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0133a0001c0001t0001g0200 | 3 | HG02717.hp1 HG02809.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.754+711T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405026 | ||||||
chr2:174405026
|
T | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+711T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405026 | ||||||
chr2:174405071
|
C | T | 2 | a0001c0001t0007g0155a0001c0001t0007g0156 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.754+756C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405071 | ||||||
chr2:174405314
|
T | C | 7 | a0000c0002t0004g0086a0001c0001t0001g0052a0001c0001t0001g0116others(4): Show | 8 | HG02109.hp2 HG02132.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+999T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405314 | ||||||
chr2:174405322
|
C | A | 7 | a0000c0002t0004g0086a0001c0001t0001g0052a0001c0001t0001g0116others(4): Show | 8 | HG02109.hp2 HG02132.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+1007C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405322 | ||||||
chr2:174405597
|
A | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1282A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405597 | ||||||
chr2:174405604
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1289G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405604 | ||||||
chr2:174405631
|
T | C | 2 | a0001c0001t0007g0155a0001c0001t0007g0156 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.754+1316T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405631 | ||||||
chr2:174405634
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+1319A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405634 | ||||||
chr2:174405838
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1523C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405838 | ||||||
chr2:174405888
|
G | C | 32 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(29): Show | 41 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.754+1573G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405888 | ||||||
chr2:174405934
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1619G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405934 | ||||||
chr2:174405991
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.754+1676G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405991 | ||||||
chr2:174406066
|
A | G | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+1751A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406066 | ||||||
chr2:174406088
|
A | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1773A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406088 | ||||||
chr2:174406197
|
G | A | 12 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(9): Show | 16 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.754+1882G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406197 | ||||||
chr2:174406267
|
A | G | 33 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(30): Show | 42 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.754+1952A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406267 | ||||||
chr2:174406294
|
G | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1979G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406294 | ||||||
chr2:174406333
|
G | T | 8 | a0001c0001t0005g0057a0001c0001t0005g0145a0001c0001t0005g0229others(5): Show | 9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+2018G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406333 | ||||||
chr2:174406383
|
A | C | 27 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(24): Show | 36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.754+2068A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406383 | ||||||
chr2:174406384
|
T | A | 27 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(24): Show | 36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.754+2069T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406384 | ||||||
chr2:174406396
|
G | A | 30 | a0000c0002t0004g0086a0000c0008t0002g0146a0001c0001t0001g0008others(27): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.754+2081G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406396 | ||||||
chr2:174406417
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+2102G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406417 | ||||||
chr2:174406508
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.754+2193G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406508 | ||||||
chr2:174406511
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+2196C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406511 | ||||||
chr2:174406543
|
C | A | 2 | a0001c0001t0007g0155a0001c0001t0007g0156 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.754+2228C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406543 | ||||||
chr2:174406549
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+2234A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406549 | ||||||
chr2:174406656
|
G | T | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+2341G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406656 | ||||||
chr2:174406702
|
C | A | 44 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(41): Show | 79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.754+2387C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406702 | ||||||
chr2:174406821
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+2506G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406821 | ||||||
chr2:174406860
|
A | C | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 77 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.754+2545A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406860 | ||||||
chr2:174406911
|
T | G | 21 | a0001c0001t0001g0162a0002c0003t0001g0004a0002c0003t0001g0019others(18): Show | 30 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.754+2596T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406911 | ||||||
chr2:174406943
|
A | G | 51 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(48): Show | 68 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.754+2628A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406943 | ||||||
chr2:174407044
|
C | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+2729C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407044 | ||||||
chr2:174407085
|
G | C | 59 | a0000c0002t0004g0086a0000c0008t0002g0146a0001c0001t0001g0008others(56): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.754+2770G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407085 | ||||||
chr2:174407101
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+2786G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407101 | ||||||
chr2:174407175
|
A | G | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.754+2860A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407175 | ||||||
chr2:174407300
|
G | A | 5 | a0001c0001t0001g0038a0001c0005t0001g0157a0001c0005t0001g0158others(2): Show | 6 | HG01891.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+2985G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407300 | ||||||
chr2:174407376
|
G | A | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754+3061G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407376 | ||||||
chr2:174407584
|
C | T | 1 | a0000c0002t0004g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.754+3269C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407584 | ||||||
chr2:174407665
|
C | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0050others(3): Show | 9 | HG02523.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.754+3350C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407665 | ||||||
chr2:174407703
|
TC | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+3389delC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407703 | ||||||
chr2:174407709
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.754+3394C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407709 | ||||||
chr2:174407765
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.754+3450C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407765 | ||||||
chr2:174407770
|
TTGAGTGG others(12): Show |
T | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.754+3461_754+3479d others(21): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174407770 | |||||
chr2:174407777
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0173 | 2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.754+3462G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407777 | ||||||
chr2:174407780
|
T | A | 1 | a0001c0001t0018g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.754+3465T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407780 | ||||||
chr2:174407880
|
G | C | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+3565G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407880 | ||||||
chr2:174407977
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.754+3662C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407977 | ||||||
chr2:174408032
|
A | G | 156 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(153): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.754+3717A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408032 | ||||||
chr2:174408116
|
A | G | 6 | a0000c0002t0002g0009a0000c0002t0002g0016a0000c0002t0002g0056others(3): Show | 14 | HG02080.hp2 HG02523.hp1 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.754+3801A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408116 | ||||||
chr2:174408163
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.754+3848A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408163 | ||||||
chr2:174408362
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4047G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408362 | ||||||
chr2:174408406
|
C | CTT | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4092_754+4093i others(4): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174408406 | |||||
chr2:174408457
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0119 | 3 | HG02055.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.754+4142T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408457 | ||||||
chr2:174408488
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4173T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408488 | ||||||
chr2:174408525
|
C | T | 1 | a0000c0002t0002g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.754+4210C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408525 | ||||||
chr2:174408554
|
C | T | 1 | a0000c0002t0002g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.754+4239C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408554 | ||||||
chr2:174408556
|
G | A | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.754+4241G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408556 | ||||||
chr2:174408588
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4273G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408588 | ||||||
chr2:174408598
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0091 | 3 | HG02258.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.754+4283G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408598 | ||||||
chr2:174408610
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.754+4295C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408610 | ||||||
chr2:174408620
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.754+4305C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408620 | ||||||
chr2:174408621
|
G | A | 58 | a0000c0002t0004g0086a0000c0008t0002g0146a0001c0001t0001g0008others(55): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.754+4306G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408621 | ||||||
chr2:174408635
|
C | A | 1 | a0002c0003t0015g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.754+4320C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408635 | ||||||
chr2:174408640
|
T | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4325T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408640 | ||||||
chr2:174408663
|
A | G | 1 | a0000c0004t0002g0025 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.754+4348A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408663 | ||||||
chr2:174408678
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.754+4363T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408678 | ||||||
chr2:174408693
|
T | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4378T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408693 | ||||||
chr2:174408698
|
T | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4383T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408698 | ||||||
chr2:174408715
|
T | C | 3 | a0001c0001t0001g0205a0003c0006t0001g0022a0006c0011t0001g0178 | 5 | HG00738.hp1 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+4400T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408715 | ||||||
chr2:174408763
|
G | C | 4 | a0000c0002t0002g0221a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02630.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+4448G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408763 | ||||||
chr2:174408777
|
A | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4462A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408777 | ||||||
chr2:174408809
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(64): Show | 115 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.754+4494G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408809 | ||||||
chr2:174408818
|
C | T | 71 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(68): Show | 94 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.754+4503C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408818 | ||||||
chr2:174408819
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4504G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408819 | ||||||
chr2:174408858
|
G | A | 1 | a0001c0001t0005g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.754+4543G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408858 | ||||||
chr2:174408863
|
C | T | 8 | a0001c0001t0003g0020a0001c0001t0003g0039a0001c0001t0003g0040others(5): Show | 13 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.754+4548C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408863 | ||||||
chr2:174408864
|
C | T | 1 | a0002c0003t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.754+4549C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408864 | ||||||
chr2:174408936
|
C | G | 1 | a0001c0001t0003g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.754+4621C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408936 | ||||||
chr2:174408953
|
C | T | 39 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(36): Show | 73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.754+4638C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408953 | ||||||
chr2:174409096
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4781C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409096 | ||||||
chr2:174409191
|
C | T | 1 | a0001c0001t0001g0013 | 4 | NA19005.hp1 NA19010.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+4876C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409191 | ||||||
chr2:174409249
|
G | A | 47 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(44): Show | 82 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.754+4934G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409249 | ||||||
chr2:174409251
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.754+4936C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409251 | ||||||
chr2:174409252
|
G | A | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+4937G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409252 | ||||||
chr2:174409260
|
A | C | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+4945A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409260 | ||||||
chr2:174409321
|
C | A | 15 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(12): Show | 19 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.754+5006C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409321 | ||||||
chr2:174409321
|
C | T | 1 | a0001c0005t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.754+5006C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409321 | ||||||
chr2:174409322
|
G | A | 21 | a0001c0001t0001g0162a0002c0003t0001g0004a0002c0003t0001g0019others(18): Show | 30 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.754+5007G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409322 | ||||||
chr2:174409434
|
C | T | 2 | a0000c0004t0002g0077a0000c0004t0002g0078 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.754+5119C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409434 | ||||||
chr2:174409460
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.754+5145G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409460 | ||||||
chr2:174409469
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.754+5154A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409469 | ||||||
chr2:174409525
|
G | A | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.754+5210G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409525 | ||||||
chr2:174409692
|
C | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0143others(1): Show | 6 | HG02615.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+5377C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409692 | ||||||
chr2:174409741
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754+5426G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409741 | ||||||
chr2:174409747
|
A | G | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0049others(4): Show | 10 | HG02165.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+5432A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409747 | ||||||
chr2:174409770
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5455C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409770 | ||||||
chr2:174409800
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5485C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409800 | ||||||
chr2:174409813
|
G | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5498G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409813 | ||||||
chr2:174409890
|
T | C | 48 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(45): Show | 87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.754+5575T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409890 | ||||||
chr2:174409916
|
G | C | 2 | a0001c0001t0001g0111a0007c0010t0001g0148 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.754+5601G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409916 | ||||||
chr2:174409960
|
GC | G | 8 | a0001c0001t0005g0057a0001c0001t0005g0145a0001c0001t0005g0229others(5): Show | 9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+5647delC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174409960 | |||||
chr2:174409999
|
T | TC | 2 | a0001c0001t0003g0039a0001c0001t0003g0040 | 4 | HG02280.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+5687dupC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174409999 | |||||
chr2:174410003
|
G | A | 8 | a0001c0001t0005g0057a0001c0001t0005g0145a0001c0001t0005g0229others(5): Show | 9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+5688G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410003 | ||||||
chr2:174410022
|
G | T | 9 | a0001c0001t0001g0164a0001c0001t0005g0057a0001c0001t0005g0145others(6): Show | 10 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+5707G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410022 | ||||||
chr2:174410023
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.754+5708C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410023 | ||||||
chr2:174410043
|
T | C | 3 | a0000c0004t0002g0025a0001c0001t0001g0182a0001c0001t0001g0212 | 4 | HG03491.hp2 HG03492.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+5728T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410043 | ||||||
chr2:174410048
|
C | G | 16 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0066others(13): Show | 26 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.754+5733C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410048 | ||||||
chr2:174410061
|
G | A | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754+5746G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410061 | ||||||
chr2:174410089
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0112others(1): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+5774C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410089 | ||||||
chr2:174410129
|
C | T | 3 | a0001c0001t0003g0058a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG02965.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.754+5814C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410129 | ||||||
chr2:174410172
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.754+5857T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410172 | ||||||
chr2:174410179
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.754+5864C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410179 | ||||||
chr2:174410180
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.754+5865G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410180 | ||||||
chr2:174410192
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.754+5877G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410192 | ||||||
chr2:174410216
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.754+5901G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410216 | ||||||
chr2:174410229
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.754+5914C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410229 | ||||||
chr2:174410273
|
C | T | 1 | a0000c0002t0002g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.754+5958C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410273 | ||||||
chr2:174410279
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5964C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410279 | ||||||
chr2:174410315
|
G | T | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+6000G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410315 | ||||||
chr2:174410318
|
C | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+6003C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410318 | ||||||
chr2:174410319
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.754+6004G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410319 | ||||||
chr2:174410321
|
G | A | 1 | a0000c0002t0002g0221 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.754+6006G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410321 | ||||||
chr2:174410334
|
T | A | 156 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(153): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.754+6019T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410334 | ||||||
chr2:174410352
|
A | C | 1 | a0001c0001t0003g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.754+6037A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410352 | ||||||
chr2:174410371
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+6056T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410371 | ||||||
chr2:174410382
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.754+6067C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410382 | ||||||
chr2:174410388
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+6073C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410388 | ||||||
chr2:174410504
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6189G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410504 | ||||||
chr2:174410549
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.754+6234C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410549 | ||||||
chr2:174410919
|
G | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+6604G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410919 | ||||||
chr2:174410923
|
G | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6608G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410923 | ||||||
chr2:174410951
|
C | T | 51 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(48): Show | 68 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.754+6636C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410951 | ||||||
chr2:174410959
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6644C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410959 | ||||||
chr2:174410983
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.754+6668T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410983 | ||||||
chr2:174410993
|
C | T | 5 | a0002c0003t0001g0035a0002c0003t0001g0138a0002c0003t0001g0139others(2): Show | 6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+6678C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410993 | ||||||
chr2:174411123
|
A | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6808A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411123 | ||||||
chr2:174411156
|
C | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6841C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411156 | ||||||
chr2:174411350
|
TG | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+7036delG | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411350 | ||||||
chr2:174411547
|
C | T | 2 | a0001c0005t0001g0158a0001c0005t0001g0159 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.754+7232C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411547 | ||||||
chr2:174411601
|
G | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+7286G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411601 | ||||||
chr2:174411605
|
A | T | 1 | a0001c0001t0001g0174 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.754+7290A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411605 | ||||||
chr2:174411609
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+7294C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411609 | ||||||
chr2:174411642
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.754+7327C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411642 | ||||||
chr2:174411702
|
A | T | 1 | a0001c0001t0003g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.754+7387A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411702 | ||||||
chr2:174411795
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+7480C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411795 | ||||||
chr2:174411836
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.754+7521G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411836 | ||||||
chr2:174411896
|
G | C | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+7581G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411896 | ||||||
chr2:174411901
|
T | G | 46 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(43): Show | 81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.754+7586T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411901 | ||||||
chr2:174411921
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.754+7606A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411921 | ||||||
chr2:174411928
|
A | T | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+7613A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411928 | ||||||
chr2:174411935
|
T | A | 235 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(232): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.754+7620T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411935 | ||||||
chr2:174411999
|
G | A | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+7684G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411999 | ||||||
chr2:174412007
|
T | C | 1 | a0001c0001t0001g0027 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.754+7692T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412007 | ||||||
chr2:174412086
|
G | T | 46 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(43): Show | 81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.754+7771G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412086 | ||||||
chr2:174412124
|
C | CA | 41 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(38): Show | 76 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.754+7819dupA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412124 | |||||
chr2:174412178
|
T | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0101 | 4 | HG03704.hp2 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+7863T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412178 | ||||||
chr2:174412242
|
G | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0142others(2): Show | 7 | HG02615.hp2 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.754+7927G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412242 | ||||||
chr2:174412351
|
A | AT | 37 | a0000c0002t0002g0055a0000c0002t0002g0216a0000c0002t0002g0217others(34): Show | 56 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.754+8050dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412351 | |||||
chr2:174412351
|
A | T | 6 | a0001c0001t0005g0057a0001c0001t0005g0229a0001c0001t0005g0231others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+8036A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412351 | ||||||
chr2:174412365
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.754+8050T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412365 | ||||||
chr2:174412499
|
AT | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+8185delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412499 | ||||||
chr2:174412517
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0166 | 3 | NA18965.hp1 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.754+8202C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412517 | ||||||
chr2:174412679
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+8364A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412679 | ||||||
chr2:174412824
|
C | T | 17 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0059others(14): Show | 27 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.754+8509C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412824 | ||||||
chr2:174412860
|
C | CT | 37 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(34): Show | 71 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.754+8569dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412860 | |||||
chr2:174412860
|
C | CTT | 7 | a0000c0002t0002g0023a0000c0002t0002g0054a0000c0002t0002g0066others(4): Show | 10 | HG00642.hp2 HG00673.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+8568_754+8569d others(4): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412860 | |||||
chr2:174412860
|
CT | C | 110 | a0000c0002t0004g0086a0000c0004t0002g0011a0000c0004t0002g0025others(107): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.754+8569delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412860 | |||||
chr2:174412891
|
G | A | 58 | a0000c0002t0004g0086a0000c0008t0002g0146a0001c0001t0001g0008others(55): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.754+8576G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412891 | ||||||
chr2:174412931
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.754+8616G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412931 | ||||||
chr2:174412962
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0021others(9): Show | 29 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.754+8647G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412962 | ||||||
chr2:174412963
|
G | C | 1 | a0002c0003t0001g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.754+8648G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412963 | ||||||
chr2:174412988
|
A | C | 155 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(152): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.754+8673A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412988 | ||||||
chr2:174413043
|
A | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+8728A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413043 | ||||||
chr2:174413100
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.754+8785G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413100 | ||||||
chr2:174413123
|
C | T | 10 | a0000c0002t0004g0006a0000c0002t0004g0024a0000c0002t0004g0060others(7): Show | 16 | HG00323.hp2 HG00639.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.754+8808C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413123 | ||||||
chr2:174413150
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+8835G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413150 | ||||||
chr2:174413159
|
A | T | 2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.754+8844A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413159 | ||||||
chr2:174413162
|
A | G | 155 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(152): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.754+8847A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413162 | ||||||
chr2:174413172
|
G | A | 29 | a0001c0001t0001g0162a0001c0001t0005g0057a0001c0001t0005g0145others(26): Show | 39 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.754+8857G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413172 | ||||||
chr2:174413384
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.754+9069A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413384 | ||||||
chr2:174413569
|
CT | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+9263delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413569 | |||||
chr2:174413586
|
C | CT | 21 | a0000c0008t0002g0146a0001c0001t0001g0031a0001c0001t0001g0038others(18): Show | 24 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.755-9277dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413586 | |||||
chr2:174413586
|
CT | C | 115 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(112): Show | 202 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.755-9277delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413586 | |||||
chr2:174413586
|
CTTTTTTT others(7): Show |
C | 6 | a0001c0001t0003g0020a0001c0001t0003g0041a0001c0001t0003g0150others(3): Show | 9 | HG00735.hp2 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+9280_755-9277d others(16): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413586 | |||||
chr2:174413653
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0163 | 8 | HG00642.hp1 HG01258.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-9232C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413653 | ||||||
chr2:174413654
|
G | A | 1 | a0000c0002t0002g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.755-9231G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413654 | ||||||
chr2:174413830
|
T | A | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-9055T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413830 | ||||||
chr2:174413880
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.755-9005C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413880 | ||||||
chr2:174414119
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.755-8766T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414119 | ||||||
chr2:174414137
|
TC | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-8745delC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174414137 | |||||
chr2:174414175
|
T | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-8710T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414175 | ||||||
chr2:174414321
|
C | T | 26 | a0000c0002t0004g0086a0001c0001t0001g0008a0001c0001t0001g0026others(23): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.755-8564C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414321 | ||||||
chr2:174414502
|
A | G | 15 | a0001c0001t0003g0020a0001c0001t0003g0039a0001c0001t0003g0040others(12): Show | 20 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.755-8383A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414502 | ||||||
chr2:174414638
|
T | C | 10 | a0001c0001t0003g0020a0001c0001t0003g0039a0001c0001t0003g0040others(7): Show | 15 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.755-8247T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414638 | ||||||
chr2:174414657
|
A | G | 7 | a0001c0001t0005g0057a0001c0001t0005g0229a0001c0001t0005g0231others(4): Show | 8 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-8228A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414657 | ||||||
chr2:174414765
|
C | CT | 127 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(124): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.755-8104dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174414765 | |||||
chr2:174414765
|
C | T | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.755-8120C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414765 | ||||||
chr2:174414910
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.755-7975C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414910 | ||||||
chr2:174414963
|
G | A | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-7922G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414963 | ||||||
chr2:174415143
|
T | C | 5 | a0000c0002t0004g0061a0000c0002t0004g0063a0000c0002t0004g0064others(2): Show | 5 | HG00323.hp2 HG02698.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.755-7742T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415143 | ||||||
chr2:174415194
|
A | G | 1 | a0001c0001t0018g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.755-7691A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415194 | ||||||
chr2:174415254
|
AT | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-7623delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174415254 | |||||
chr2:174415297
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0132 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.755-7588T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415297 | ||||||
chr2:174415386
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-7499A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415386 | ||||||
chr2:174415552
|
A | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02630.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-7333A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415552 | ||||||
chr2:174415590
|
A | T | 1 | a0001c0001t0003g0041 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.755-7295A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415590 | ||||||
chr2:174415606
|
T | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-7279T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415606 | ||||||
chr2:174415643
|
G | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-7242G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415643 | ||||||
chr2:174415671
|
G | A | 1 | a0001c0001t0013g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755-7214G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415671 | ||||||
chr2:174415675
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-7210C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415675 | ||||||
chr2:174415770
|
A | G | 46 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(43): Show | 81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.755-7115A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415770 | ||||||
chr2:174415914
|
A | G | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-6971A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415914 | ||||||
chr2:174415965
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.755-6920G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415965 | ||||||
chr2:174416094
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.755-6791A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416094 | ||||||
chr2:174416256
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-6629G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416256 | ||||||
chr2:174416320
|
A | T | 1 | a0000c0002t0002g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.755-6565A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416320 | ||||||
chr2:174416334
|
A | G | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.755-6551A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416334 | ||||||
chr2:174416642
|
G | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0172 | 3 | NA18954.hp1 NA18991.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.755-6243G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416642 | ||||||
chr2:174416653
|
T | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-6232T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416653 | ||||||
chr2:174416659
|
A | G | 1 | a0001c0001t0001g0014 | 4 | HG00558.hp2 NA18950.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.755-6226A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416659 | ||||||
chr2:174416668
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.755-6217A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416668 | ||||||
chr2:174416740
|
T | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 12 | HG00733.hp1 HG01346.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.755-6145T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416740 | ||||||
chr2:174416755
|
T | G | 2 | a0000c0002t0002g0053a0000c0002t0002g0222 | 3 | NA18974.hp2 NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.755-6130T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416755 | ||||||
chr2:174416757
|
C | T | 1 | a0000c0004t0002g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.755-6128C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416757 | ||||||
chr2:174416850
|
G | A | 8 | a0001c0001t0005g0057a0001c0001t0005g0145a0001c0001t0005g0229others(5): Show | 9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.755-6035G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416850 | ||||||
chr2:174417229
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.755-5656C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417229 | ||||||
chr2:174417272
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-5613C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417272 | ||||||
chr2:174417375
|
T | A | 1 | a0002c0003t0001g0135 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.755-5510T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417375 | ||||||
chr2:174417436
|
T | C | 43 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(40): Show | 78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-5449T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417436 | ||||||
chr2:174417577
|
T | G | 4 | a0001c0005t0001g0157a0001c0005t0001g0158a0001c0005t0001g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.755-5308T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417577 | ||||||
chr2:174417635
|
C | T | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-5250C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417635 | ||||||
chr2:174417682
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0192 | 7 | HG00558.hp2 NA18948.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.755-5203C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417682 | ||||||
chr2:174417825
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.755-5060C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417825 | ||||||
chr2:174417980
|
A | G | 1 | a0002c0003t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.755-4905A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417980 | ||||||
chr2:174418008
|
T | C | 200 | a0000c0002t0004g0086a0000c0004t0002g0011a0000c0004t0002g0025others(197): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.755-4877T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418008 | ||||||
chr2:174418169
|
T | C | 1 | a0003c0006t0001g0022 | 3 | HG00738.hp1 HG01496.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.755-4716T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418169 | ||||||
chr2:174418241
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-4644A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418241 | ||||||
chr2:174418322
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-4563G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418322 | ||||||
chr2:174418411
|
G | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0154others(16): Show | 25 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.755-4474G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418411 | ||||||
chr2:174419011
|
T | C | 1 | a0001c0001t0001g0026 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755-3874T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419011 | ||||||
chr2:174419086
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.755-3799G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419086 | ||||||
chr2:174419328
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.755-3557T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419328 | ||||||
chr2:174419432
|
T | C | 1 | a0001c0001t0003g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.755-3453T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419432 | ||||||
chr2:174419493
|
C | T | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.755-3392C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419493 | ||||||
chr2:174419539
|
C | G | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.755-3346C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419539 | ||||||
chr2:174419543
|
C | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-3342C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419543 | ||||||
chr2:174419572
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02630.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-3313G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419572 | ||||||
chr2:174419586
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.755-3299G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419586 | ||||||
chr2:174419612
|
CTCACAGT others(1): Show |
C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-3269_755-3262d others(10): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174419612 | |||||
chr2:174419621
|
T | C | 1 | a0000c0002t0002g0224 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.755-3264T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419621 | ||||||
chr2:174419740
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3145C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419740 | ||||||
chr2:174419841
|
G | A | 1 | a0008c0012t0001g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.755-3044G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419841 | ||||||
chr2:174419842
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.755-3043G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419842 | ||||||
chr2:174419969
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0091 | 3 | HG02258.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755-2916A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419969 | ||||||
chr2:174420173
|
AT | A | 155 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(152): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.755-2703delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174420173 | |||||
chr2:174420178
|
T | C | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755-2707T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420178 | ||||||
chr2:174420230
|
C | T | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755-2655C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420230 | ||||||
chr2:174420231
|
G | A | 1 | a0001c0001t0013g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755-2654G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420231 | ||||||
chr2:174420396
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0132 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.755-2489C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420396 | ||||||
chr2:174420397
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.755-2488G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420397 | ||||||
chr2:174420567
|
A | G | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755-2318A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420567 | ||||||
chr2:174420729
|
A | G | 1 | a0002c0003t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.755-2156A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420729 | ||||||
chr2:174420749
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0100 | 3 | HG00280.hp1 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.755-2136G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420749 | ||||||
chr2:174421041
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0179 | 7 | NA18945.hp2 NA19002.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-1844G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421041 | ||||||
chr2:174421142
|
G | T | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.755-1743G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421142 | ||||||
chr2:174421143
|
A | C | 109 | a0000c0002t0004g0086a0000c0004t0002g0011a0000c0004t0002g0025others(106): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.755-1742A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421143 | ||||||
chr2:174421251
|
A | G | 112 | a0000c0002t0004g0086a0000c0004t0002g0011a0000c0004t0002g0025others(109): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.755-1634A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421251 | ||||||
chr2:174421255
|
A | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-1630A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421255 | ||||||
chr2:174421334
|
T | C | 7 | a0001c0001t0005g0057a0001c0001t0005g0229a0001c0001t0005g0231others(4): Show | 8 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-1551T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421334 | ||||||
chr2:174421519
|
A | G | 1 | a0004c0007t0010g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.755-1366A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421519 | ||||||
chr2:174421880
|
C | T | 12 | a0000c0004t0002g0011a0000c0004t0002g0025a0000c0004t0002g0071others(9): Show | 16 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.755-1005C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421880 | ||||||
chr2:174421957
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-928G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421957 | ||||||
chr2:174422215
|
C | T | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.755-670C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422215 | ||||||
chr2:174422247
|
A | G | 155 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(152): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.755-638A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422247 | ||||||
chr2:174422321
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-564C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422321 | ||||||
chr2:174422454
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-431G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422454 | ||||||
chr2:174422468
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0097 | 2 | HG01099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.755-417G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422468 | ||||||
chr2:174422528
|
T | C | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-357T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422528 | ||||||
chr2:174422538
|
C | T | 1 | a0000c0002t0002g0224 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.755-347C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422538 | ||||||
chr2:174422555
|
A | G | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-330A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422555 | ||||||
chr2:174422569
|
C | CA | 36 | a0000c0002t0004g0086a0000c0004t0002g0073a0000c0004t0002g0075others(33): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.755-298dupA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174422569 | |||||
chr2:174422569
|
CA | C | 25 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0056others(22): Show | 36 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.755-298delA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174422569 | |||||
chr2:174422646
|
AT | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-232delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174422646 | |||||
chr2:174423050
|
G | A | 38 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(35): Show | 72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.917+3G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423050 | ||||||
chr2:174423279
|
G | A | 6 | a0001c0001t0005g0057a0001c0001t0005g0229a0001c0001t0005g0231others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.917+232G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423279 | ||||||
chr2:174423281
|
A | T | 34 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0016others(31): Show | 66 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.917+234A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423281 | ||||||
chr2:174423500
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 128 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.917+453C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423500 | ||||||
chr2:174423501
|
G | A | 1 | a0002c0003t0014g0136 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.917+454G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423501 | ||||||
chr2:174423612
|
T | C | 17 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0066others(14): Show | 27 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.917+565T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423612 | ||||||
chr2:174423663
|
G | T | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.917+616G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423663 | ||||||
chr2:174423761
|
A | G | 1 | a0001c0001t0005g0145 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.917+714A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423761 | ||||||
chr2:174423764
|
C | T | 2 | a0002c0003t0001g0138a0002c0003t0001g0140 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.918-711C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423764 | ||||||
chr2:174423777
|
C | CT | 28 | a0001c0001t0001g0034a0001c0001t0001g0098a0001c0001t0001g0122others(25): Show | 32 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.918-672dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | |||||
chr2:174423777
|
C | CTT | 14 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0112others(11): Show | 19 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.918-673_918-672dup others(2): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | |||||
chr2:174423777
|
CT | C | 18 | a0000c0002t0002g0002a0000c0002t0002g0023a0000c0002t0002g0053others(15): Show | 32 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.918-672delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | |||||
chr2:174423777
|
CTT | C | 17 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0059others(14): Show | 27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.918-673_918-672del others(2): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | |||||
chr2:174423777
|
CTTT | C | 10 | a0000c0002t0002g0066a0000c0004t0002g0011a0000c0004t0002g0025others(7): Show | 14 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.918-674_918-672del others(3): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | |||||
chr2:174423779
|
T | TC | 4 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0171others(1): Show | 4 | HG06807.hp1 NA18965.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.918-696_918-695ins others(1): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423779 | ||||||
chr2:174423780
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 126 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.918-695T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423780 | ||||||
chr2:174423781
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.918-694T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423781 | ||||||
chr2:174423824
|
C | T | 2 | a0001c0001t0001g0111a0007c0010t0001g0148 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.918-651C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423824 | ||||||
chr2:174423848
|
T | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.918-627T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423848 | ||||||
chr2:174423970
|
G | T | 75 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(72): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.918-505G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423970 | ||||||
chr2:174423980
|
G | T | 1 | a0001c0001t0016g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.918-495G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423980 | ||||||
chr2:174424127
|
C | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027others(29): Show | 41 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(38): Show |
intron_variant | MODIFIER | c.918-348C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424127 | ||||||
chr2:174424161
|
G | T | 1 | a0000c0002t0002g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.918-314G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424161 | ||||||
chr2:174424257
|
G | T | 1 | a0000c0002t0002g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.918-218G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424257 | ||||||
chr2:174424416
|
C | A | 50 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(47): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.918-59C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424416 | ||||||
chr2:174424691
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0132 | 3 | HG02280.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1092+42G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424691 | ||||||
chr2:174424704
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1092+55C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424704 | ||||||
chr2:174424774
|
G | A | 2 | a0004c0007t0010g0109a0004c0007t0010g0110 | 2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1092+125G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424774 | ||||||
chr2:174424822
|
C | T | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+173C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424822 | ||||||
chr2:174424898
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1092+249T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424898 | ||||||
chr2:174424963
|
G | T | 1 | a0000c0002t0002g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1092+314G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424963 | ||||||
chr2:174425006
|
G | A | 231 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(228): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1092+357G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425006 | ||||||
chr2:174425104
|
C | T | 1 | a0000c0002t0002g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1092+455C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425104 | ||||||
chr2:174425257
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+608G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425257 | ||||||
chr2:174425279
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1092+630G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425279 | ||||||
chr2:174425643
|
T | C | 50 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(47): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1092+994T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425643 | ||||||
chr2:174425917
|
A | G | 20 | a0002c0003t0001g0004a0002c0003t0001g0019a0002c0003t0001g0035others(17): Show | 29 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1092+1268A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425917 | ||||||
chr2:174426038
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1092+1389A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426038 | ||||||
chr2:174426089
|
T | C | 1 | a0000c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+1440T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426089 | ||||||
chr2:174426092
|
G | A | 50 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(47): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1092+1443G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426092 | ||||||
chr2:174426314
|
A | T | 18 | a0000c0002t0002g0010a0000c0002t0002g0017a0000c0002t0002g0059others(15): Show | 28 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1093-1399A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426314 | ||||||
chr2:174426420
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1093-1293C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426420 | ||||||
chr2:174426646
|
C | A | 2 | a0000c0002t0004g0062a0000c0002t0004g0065 | 2 | HG01515.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1093-1067C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426646 | ||||||
chr2:174426735
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1093-978G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426735 | ||||||
chr2:174426771
|
C | CCAAAA | 31 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027others(28): Show | 40 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(37): Show |
intron_variant | MODIFIER | c.1093-921_1093-917d others(7): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 174426771 | |||||
chr2:174426815
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-898C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426815 | ||||||
chr2:174426816
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-897A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426816 | ||||||
chr2:174426817
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-896C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426817 | ||||||
chr2:174426823
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-890A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426823 | ||||||
chr2:174426832
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-881T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426832 | ||||||
chr2:174426837
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-876T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426837 | ||||||
chr2:174426838
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-875A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426838 | ||||||
chr2:174426842
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-871A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426842 | ||||||
chr2:174426846
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-867A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426846 | ||||||
chr2:174426850
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-863T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426850 | ||||||
chr2:174426856
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-857A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426856 | ||||||
chr2:174426882
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-831G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426882 | ||||||
chr2:174426896
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-817G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426896 | ||||||
chr2:174426897
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-816A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426897 | ||||||
chr2:174426919
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1093-794G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426919 | ||||||
chr2:174427021
|
C | T | 50 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(47): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1093-692C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427021 | ||||||
chr2:174427076
|
C | T | 20 | a0002c0003t0001g0004a0002c0003t0001g0019a0002c0003t0001g0035others(17): Show | 29 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1093-637C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427076 | ||||||
chr2:174427109
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0147others(2): Show | 6 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093-604C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427109 | ||||||
chr2:174427155
|
T | C | 50 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(47): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1093-558T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427155 | ||||||
chr2:174427318
|
A | G | 1 | a0001c0001t0001g0046 | 2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1093-395A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427318 | ||||||
chr2:174427506
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1093-207A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427506 | ||||||
chr2:174427598
|
C | A | 104 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027others(101): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1093-115C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427598 | ||||||
chr2:174427636
|
T | C | 50 | a0000c0002t0002g0002a0000c0002t0002g0009a0000c0002t0002g0010others(47): Show | 88 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1093-77T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427636 |