geneid | 9887 |
---|---|
ensemblid | ENSG00000116698.22 |
hgncid | 16792 |
symbol | SMG7 |
name | SMG7 nonsense mediated mRNA decay factor |
refseq_nuc | NM_001375584.1 |
refseq_prot | NP_001362513.1 |
ensembl_nuc | ENST00000688051.1 |
ensembl_prot | ENSP00000510175.1 |
mane_status | MANE Select |
chr | chr1 |
start | 183472499 |
end | 183554191 |
strand | + |
ver | v1.2 |
region | chr1:183472499-183554191 |
region5000 | chr1:183467499-183559191 |
regionname0 | SMG7_chr1_183472499_183554191 |
regionname5000 | SMG7_chr1_183467499_183559191 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1187 | 229 | 60 | 42 | 94 | 10 | 21 | 71 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0002 | 0/0 | 1187 | 69 | 20 | 15 | 25 | 4 | 5 | 21 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0003 | 0/0 | 1187 | 44 | 0 | 4 | 38 | 0 | 2 | 30 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0004 | 0/0 | 1188 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0005 | 0/0 | 1187 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0006 | 0/0 | 1187 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0007 | 0/0 | 1187 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0008 | 0/0 | 1187 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0009 | 0/0 | 1187 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0010 | 0/0 | 1187 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3564 | 212 | 57 | 37 | 92 | 6 | 19 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0002 | 0/0 | 3564 | 69 | 20 | 15 | 25 | 4 | 5 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0003 | 0/0 | 3564 | 44 | 0 | 4 | 38 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0004 | 1/0 | 3564 | 14 | 2 | 5 | 0 | 4 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0005 | 0/0 | 3567 | 8 | 8 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0006 | 0/0 | 3564 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0007 | 0/0 | 3564 | 2 | 1 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0008 | 0/0 | 3564 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0009 | 0/0 | 3564 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0010 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0011 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0012 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0013 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
c0014 | 0/0 | 3564 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2383 | 151 | 38 | 25 | 65 | 8 | 13 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0002 | 0/0 | 2377 | 62 | 19 | 15 | 21 | 3 | 4 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0003 | 0/0 | 2386 | 43 | 3 | 11 | 26 | 0 | 3 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0004 | 0/0 | 2385 | 27 | 4 | 5 | 16 | 1 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0005 | 0/0 | 2383 | 19 | 13 | 3 | 1 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0006 | 0/0 | 2387 | 17 | 1 | 3 | 10 | 1 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0007 | 0/0 | 2384 | 13 | 6 | 2 | 5 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0008 | 0/0 | 2378 | 4 | 0 | 0 | 3 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0009 | 0/0 | 2383 | 4 | 2 | 0 | 1 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0010 | 0/0 | 2383 | 4 | 0 | 0 | 4 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0011 | 0/0 | 2385 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0012 | 0/0 | 2380 | 2 | 0 | 0 | 1 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0013 | 0/0 | 2385 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0014 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0015 | 0/0 | 2383 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0016 | 0/0 | 2387 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0017 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0018 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0019 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0020 | 0/0 | 2387 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0021 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
t0022 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3564 | 212 | 57 | 37 | 92 | 6 | 19 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0004 | 1/0 | 3564 | 14 | 2 | 5 | 0 | 4 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0010 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0012 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0014 | 0/0 | 3564 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0002c0002 | 0/0 | 3564 | 69 | 20 | 15 | 25 | 4 | 5 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0003c0003 | 0/0 | 3564 | 44 | 0 | 4 | 38 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0004c0005 | 0/0 | 3567 | 8 | 8 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0005c0006 | 0/0 | 3564 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0006c0008 | 0/0 | 3564 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0007c0007 | 0/0 | 3564 | 2 | 1 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0008c0009 | 0/0 | 3564 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0009c0011 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0010c0013 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5946 | 86 | 35 | 14 | 23 | 4 | 9 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0003 | 0/0 | 5949 | 43 | 3 | 11 | 26 | 0 | 3 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0004 | 0/0 | 5948 | 26 | 4 | 5 | 15 | 1 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0005 | 0/0 | 5946 | 8 | 3 | 2 | 1 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0006 | 0/0 | 5950 | 16 | 1 | 3 | 9 | 1 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0007 | 0/0 | 5947 | 12 | 5 | 2 | 5 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0009 | 0/0 | 5946 | 3 | 2 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0010 | 0/0 | 5946 | 4 | 0 | 0 | 4 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0011 | 0/0 | 5948 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0013 | 0/0 | 5948 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0014 | 0/0 | 5948 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0015 | 0/0 | 5946 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0016 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0017 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0018 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0019 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0020 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0021 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0001t0022 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0004t0001 | 1/0 | 5946 | 14 | 2 | 5 | 0 | 4 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0010t0009 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0012t0006 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0001c0014t0001 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0002c0002t0002 | 0/0 | 5940 | 62 | 19 | 15 | 21 | 3 | 4 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0002c0002t0005 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0002c0002t0008 | 0/0 | 5941 | 4 | 0 | 0 | 3 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0002c0002t0012 | 0/0 | 5943 | 2 | 0 | 0 | 1 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0003c0003t0001 | 0/0 | 5946 | 43 | 0 | 4 | 37 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0003c0003t0004 | 0/0 | 5948 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0004c0005t0005 | 0/0 | 5949 | 8 | 8 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0005c0006t0001 | 0/0 | 5946 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0006c0008t0001 | 0/0 | 5946 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0007c0007t0005 | 0/0 | 5946 | 2 | 1 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0008c0009t0007 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0009c0011t0001 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
a0010c0013t0001 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | copy fasta | chr1 | 183467499 | 183559191 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0011g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0011g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0013g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0015g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0016g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0017g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0018g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0019g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0020g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0021g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0001t0022g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0010t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0012t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0001c0014t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0002c0002t0012g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0003c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0004c0005t0005g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0004c0005t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0004c0005t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0004c0005t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0004c0005t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0004c0005t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0005c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0005c0006t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0005c0006t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0006c0008t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0006c0008t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0007c0007t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0007c0007t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0008c0009t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0009c0011t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
a0010c0013t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0088 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00140 | hp1 | a0002 | c0002 | t0012 | g0068 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0022 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0324 | EUR | FIN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00280 | hp2 | a0001 | c0004 | t0001 | g0083 | EUR | FIN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0120 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0241 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0089 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01069 | hp2 | a0007 | c0007 | t0005 | g0172 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0132 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01167 | hp2 | a0001 | c0004 | t0001 | g0092 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0017 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0091 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0208 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0090 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0017 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0084 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01261 | hp2 | a0006 | c0008 | t0001 | g0323 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0210 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01516 | hp1 | a0001 | c0004 | t0001 | g0087 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0059 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0060 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0099 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0219 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0194 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0067 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02004 | hp2 | a0003 | c0003 | t0001 | g0119 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02015 | hp1 | a0009 | c0011 | t0001 | g0014 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02015 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0187 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02055 | hp1 | a0004 | c0005 | t0005 | g0167 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02056 | hp2 | a0001 | c0001 | t0010 | g0189 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02074 | hp1 | a0001 | c0001 | t0022 | g0235 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02080 | hp2 | a0002 | c0002 | t0012 | g0062 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02132 | hp2 | a0001 | c0001 | t0020 | g0006 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02145 | hp2 | a0004 | c0005 | t0005 | g0170 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0122 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02258 | hp1 | a0002 | c0002 | t0005 | g0043 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0265 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02293 | hp1 | a0006 | c0008 | t0001 | g0318 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02523 | hp1 | a0001 | c0001 | t0021 | g0287 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02523 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02572 | hp2 | a0004 | c0005 | t0005 | g0005 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0076 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02622 | hp1 | a0004 | c0005 | t0005 | g0169 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0204 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02717 | hp2 | a0001 | c0014 | t0001 | g0130 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02723 | hp1 | a0001 | c0001 | t0019 | g0184 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0080 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02895 | hp1 | a0004 | c0005 | t0005 | g0166 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0174 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02897 | hp2 | a0004 | c0005 | t0005 | g0005 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02922 | hp1 | a0004 | c0005 | t0005 | g0168 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02922 | hp2 | a0007 | c0007 | t0005 | g0171 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03130 | hp2 | a0004 | c0005 | t0005 | g0005 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03491 | hp1 | a0001 | c0004 | t0001 | g0093 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0255 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0135 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0262 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0143 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03927 | hp1 | a0002 | c0002 | t0008 | g0071 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0232 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0006 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0254 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0058 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG04228 | hp1 | a0001 | c0001 | t0015 | g0127 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18612 | hp1 | a0001 | c0001 | t0017 | g0185 | EAS | CHB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | CHB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18949 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18953 | hp1 | a0002 | c0002 | t0008 | g0052 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18954 | hp2 | a0001 | c0010 | t0009 | g0199 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18961 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18961 | hp2 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18963 | hp2 | a0003 | c0003 | t0001 | g0131 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18967 | hp1 | a0002 | c0002 | t0008 | g0057 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18971 | hp1 | a0001 | c0001 | t0013 | g0268 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18971 | hp2 | a0003 | c0003 | t0004 | g0234 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18972 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18973 | hp1 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18983 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18988 | hp1 | a0005 | c0006 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18990 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18991 | hp1 | a0002 | c0002 | t0008 | g0049 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18993 | hp2 | a0003 | c0003 | t0001 | g0136 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19001 | hp2 | a0001 | c0001 | t0011 | g0279 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19003 | hp1 | a0001 | c0001 | t0011 | g0273 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19006 | hp1 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19007 | hp1 | a0001 | c0001 | t0013 | g0269 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19007 | hp2 | a0005 | c0006 | t0001 | g0309 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19009 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19012 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19012 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0180 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19072 | hp1 | a0005 | c0006 | t0001 | g0310 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19072 | hp2 | a0001 | c0001 | t0007 | g0217 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19076 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19078 | hp1 | a0001 | c0012 | t0006 | g0248 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19078 | hp2 | a0010 | c0013 | t0001 | g0296 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0133 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19082 | hp2 | a0001 | c0001 | t0011 | g0278 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19086 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0222 | AFR | ASW | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0085 | EUR | TSI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0216 | EUR | TSI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0086 | SAS | GIH | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | GIH | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0157 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0181 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
NA21309 | hp2 | a0008 | c0009 | t0007 | g0198 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0097 | REF | REF | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183526605
|
G | A | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.322G>A | p.Glu108Lys | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 444/5946 | 322/3564 | 108/1187 | chr1 | 183526605 | ||
chr1:183526677
|
A | G | 1 | a0006 | 2 | HG01261.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.394A>G | p.Lys132Glu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 516/5946 | 394/3564 | 132/1187 | chr1 | 183526677 | ||
chr1:183526681
|
A | G | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.398A>G | p.Gln133Arg | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 520/5946 | 398/3564 | 133/1187 | chr1 | 183526681 | ||
chr1:183526706
|
G | C | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.423G>C | p.Lys141Asn | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 545/5946 | 423/3564 | 141/1187 | chr1 | 183526706 | ||
chr1:183526707
|
C | G | 1 | a0010 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.424C>G | p.Pro142Ala | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 546/5946 | 424/3564 | 142/1187 | chr1 | 183526707 | ||
chr1:183529445
|
C | T | 2 | a0005a0010 | 4 | NA18988.hp1 NA19007.hp2 NA19072.hp1 others(1): Show |
missense_variant | MODERATE | c.755C>T | p.Ala252Val | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/23 | 877/5946 | 755/3564 | 252/1187 | chr1 | 183529445 | ||
chr1:183533735
|
T | TACA | 1 | a0004 | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.1068_1070dupCAA | p.Asn357dup | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/23 | 1193/5946 | 1071/3564 | 357/1187 | INFO_REALIGN_3_PRIME | chr1 | 183533735 | |
chr1:183546293
|
G | A | 1 | a0002 | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
missense_variant | MODERATE | c.2698G>A | p.Val900Ile | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/23 | 2820/5946 | 2698/3564 | 900/1187 | chr1 | 183546293 | ||
chr1:183547106
|
C | T | 2 | a0003a0009 | 45 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(42): Show |
missense_variant | MODERATE | c.2746C>T | p.Pro916Ser | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/23 | 2868/5946 | 2746/3564 | 916/1187 | chr1 | 183547106 | ||
chr1:183547136
|
C | A | 1 | a0009 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2776C>A | p.Leu926Met | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/23 | 2898/5946 | 2776/3564 | 926/1187 | chr1 | 183547136 | ||
chr1:183549767
|
A | G | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2977A>G | p.Arg993Gly | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/23 | 3099/5946 | 2977/3564 | 993/1187 | chr1 | 183549767 | ||
chr1:183550908
|
A | C | 1 | a0007 | 2 | HG01069.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.3291A>C | p.Lys1097Asn | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 21/23 | 3413/5946 | 3291/3564 | 1097/1187 | chr1 | 183550908 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183515944
|
A | G | 1 | a0001c0014 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.132A>G | p.Leu44Leu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/23 | 254/5946 | 132/3564 | 44/1187 | chr1 | 183515944 | ||
chr1:183517724
|
G | A | 13 | a0001c0001a0001c0010a0001c0012others(10): Show | 346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
synonymous_variant | LOW | c.216G>A | p.Leu72Leu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/23 | 338/5946 | 216/3564 | 72/1187 | chr1 | 183517724 | ||
chr1:183526604
|
A | G | 1 | a0010c0013 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.321A>G | p.Gln107Gln | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 443/5946 | 321/3564 | 107/1187 | chr1 | 183526604 | ||
chr1:183526607
|
A | G | 1 | a0010c0013 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.324A>G | p.Glu108Glu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 446/5946 | 324/3564 | 108/1187 | chr1 | 183526607 | ||
chr1:183526682
|
G | A | 1 | a0010c0013 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.399G>A | p.Gln133Gln | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 521/5946 | 399/3564 | 133/1187 | chr1 | 183526682 | ||
chr1:183546058
|
C | T | 1 | a0001c0012 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.2463C>T | p.Tyr821Tyr | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/23 | 2585/5946 | 2463/3564 | 821/1187 | chr1 | 183546058 | ||
chr1:183549216
|
A | G | 1 | a0001c0010 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.2901A>G | p.Leu967Leu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 19/23 | 3023/5946 | 2901/3564 | 967/1187 | chr1 | 183549216 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183552040
|
C | T | 1 | a0001c0001t0022 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 109 | chr1 | 183552040 | |||||
chr1:183552086
|
C | T | 1 | a0001c0001t0021 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 155 | chr1 | 183552086 | |||||
chr1:183552148
|
C | T | 22 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(19): Show | 203 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 217 | chr1 | 183552148 | |||||
chr1:183552176
|
G | A | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 245 | chr1 | 183552176 | |||||
chr1:183552267
|
A | G | 1 | a0001c0001t0020 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 336 | chr1 | 183552267 | |||||
chr1:183552375
|
ATTATTC | A | 3 | a0002c0002t0002a0002c0002t0008a0002c0002t0012 | 68 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*448_*453delTTCTTA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 448 | INFO_REALIGN_3_PRIME | chr1 | 183552375 | ||||
chr1:183552580
|
G | C | 1 | a0001c0001t0013 | 2 | NA18971.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*649G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 649 | chr1 | 183552580 | |||||
chr1:183553128
|
G | A | 1 | a0001c0001t0015 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1197 | chr1 | 183553128 | |||||
chr1:183553406
|
G | T | 1 | a0001c0001t0011 | 3 | NA19001.hp2 NA19003.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1475G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1475 | chr1 | 183553406 | |||||
chr1:183553573
|
A | AT | 3 | a0001c0001t0014a0001c0001t0018a0001c0001t0019 | 3 | HG02723.hp1 HG03471.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1643dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1644 | INFO_REALIGN_3_PRIME | chr1 | 183553573 | ||||
chr1:183553608
|
G | GC | 4 | a0001c0001t0007a0001c0001t0014a0002c0002t0008others(1): Show | 18 | HG00735.hp1 HG01993.hp1 HG02970.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1685dupC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | ||||
chr1:183553608
|
G | GCC | 4 | a0001c0001t0004a0001c0001t0011a0001c0001t0013others(1): Show | 32 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1684_*1685dupCC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | ||||
chr1:183553608
|
G | GCCC | 3 | a0001c0001t0003a0001c0001t0022a0002c0002t0012 | 46 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1685dupCCC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | ||||
chr1:183553608
|
G | GCCCC | 4 | a0001c0001t0006a0001c0001t0016a0001c0001t0020others(1): Show | 19 | HG01169.hp2 HG01943.hp2 HG02080.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1682_*1685dupCCCC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | ||||
chr1:183553616
|
C | T | 1 | a0001c0001t0017 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1685 | chr1 | 183553616 | |||||
chr1:183553617
|
G | C | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(12): Show | 114 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1686G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | chr1 | 183553617 | |||||
chr1:183553936
|
A | G | 1 | a0001c0001t0010 | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2005A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 2005 | chr1 | 183553936 | |||||
chr1:183554068
|
G | A | 1 | a0001c0001t0010 | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2137G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 2137 | chr1 | 183554068 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:183472701
|
G | C | 1 | a0001c0001t0003g0025 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.29+52G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472701 | ||||||
chr1:183472711
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.29+62A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472711 | ||||||
chr1:183472811
|
G | A | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.29+162G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472811 | ||||||
chr1:183472842
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(44): Show | 53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.29+193C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472842 | ||||||
chr1:183472856
|
G | A | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+207G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472856 | ||||||
chr1:183472932
|
G | C | 1 | a0002c0002t0002g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.29+283G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472932 | ||||||
chr1:183472962
|
C | T | 103 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(100): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.29+313C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472962 | ||||||
chr1:183472967
|
A | G | 1 | a0001c0001t0003g0281 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.29+318A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472967 | ||||||
chr1:183472999
|
G | A | 1 | a0001c0001t0006g0190 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.29+350G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472999 | ||||||
chr1:183473015
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.29+366C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473015 | ||||||
chr1:183473040
|
G | A | 4 | a0002c0002t0002g0008a0002c0002t0002g0028a0002c0002t0002g0029others(1): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.29+391G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473040 | ||||||
chr1:183473185
|
G | C | 1 | a0001c0001t0003g0191 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.29+536G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473185 | ||||||
chr1:183473189
|
A | C | 42 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0010others(39): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.29+540A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473189 | ||||||
chr1:183473362
|
T | G | 16 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0044others(13): Show | 19 | HG00558.hp2 HG00609.hp2 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.29+713T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473362 | ||||||
chr1:183473402
|
G | A | 11 | a0001c0004t0001g0083a0001c0004t0001g0084a0001c0004t0001g0085others(8): Show | 11 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.29+753G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473402 | ||||||
chr1:183473659
|
T | TG | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+1014dupG | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183473659 | |||||
chr1:183473973
|
A | T | 10 | a0001c0001t0003g0025a0001c0001t0003g0191a0001c0001t0003g0275others(7): Show | 10 | HG00408.hp2 HG02056.hp1 NA19001.hp2 others(7): Show |
intron_variant | MODIFIER | c.29+1324A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473973 | ||||||
chr1:183474039
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.29+1390C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474039 | ||||||
chr1:183474160
|
G | A | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+1511G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474160 | ||||||
chr1:183474296
|
CTCACGCC others(5): Show |
C | 1 | a0001c0001t0017g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.29+1650_29+1661del others(12): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183474296 | |||||
chr1:183474650
|
A | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(328): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.29+2001A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474650 | ||||||
chr1:183474766
|
C | T | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.29+2117C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474766 | ||||||
chr1:183474875
|
G | C | 1 | a0003c0003t0001g0098 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.29+2226G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474875 | ||||||
chr1:183474925
|
G | A | 5 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0197others(2): Show | 5 | HG01257.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.29+2276G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474925 | ||||||
chr1:183474929
|
G | A | 22 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.29+2280G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474929 | ||||||
chr1:183475154
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.29+2505C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475154 | ||||||
chr1:183475229
|
G | A | 2 | a0003c0003t0001g0110a0003c0003t0001g0111 | 2 | NA19076.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.29+2580G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475229 | ||||||
chr1:183475313
|
A | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.29+2664A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475313 | ||||||
chr1:183475445
|
G | T | 1 | a0003c0003t0001g0182 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.29+2796G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475445 | ||||||
chr1:183475879
|
GA | G | 39 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0024others(36): Show | 41 | HG00544.hp1 HG00597.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.29+3238delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183475879 | |||||
chr1:183476147
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.29+3498G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476147 | ||||||
chr1:183476233
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29+3584T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476233 | ||||||
chr1:183476728
|
A | G | 1 | a0001c0001t0003g0272 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.29+4079A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476728 | ||||||
chr1:183476745
|
TTTG | T | 57 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(54): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.29+4099_29+4101del others(3): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183476745 | |||||
chr1:183476969
|
G | A | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+4320G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476969 | ||||||
chr1:183477242
|
T | C | 1 | a0001c0001t0014g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.29+4593T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477242 | ||||||
chr1:183477398
|
T | TTG | 118 | a0001c0001t0001g0156a0001c0001t0003g0002a0001c0001t0003g0006others(115): Show | 121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.29+4769_29+4770dup others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477398 | |||||
chr1:183477398
|
TTGTG | T | 40 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0010others(37): Show | 46 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.29+4767_29+4770del others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477398 | |||||
chr1:183477400
|
G | T | 2 | a0001c0001t0014g0157a0001c0001t0018g0181 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.29+4751G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477400 | ||||||
chr1:183477402
|
G | T | 1 | a0001c0001t0014g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.29+4753G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477402 | ||||||
chr1:183477416
|
G | A | 1 | a0002c0002t0002g0044 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29+4767G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477416 | ||||||
chr1:183477419
|
T | TGTGCATA others(21): Show |
1 | a0002c0002t0002g0044 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29+4770_29+4771ins others(28): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477419 | ||||||
chr1:183477420
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.29+4771A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477420 | ||||||
chr1:183477442
|
A | G | 1 | a0002c0002t0002g0044 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29+4793A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477442 | ||||||
chr1:183477452
|
A | ATGTGTGC others(27): Show |
84 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(81): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.29+4835_29+4836ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477452 | |||||
chr1:183477452
|
A | ATGTGTGC others(61): Show |
13 | a0001c0001t0003g0025a0001c0001t0003g0191a0001c0001t0003g0275others(10): Show | 13 | HG00408.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.29+4835_29+4836ins others(68): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477452 | |||||
chr1:183477452
|
A | ATGTGTGC others(27): Show |
4 | a0001c0001t0003g0270a0001c0001t0003g0271a0001c0001t0013g0268others(1): Show | 4 | NA18971.hp1 NA19007.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+4832_29+4833ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477452 | |||||
chr1:183477457
|
T | TGCATATG others(27): Show |
1 | a0001c0010t0009g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.29+4835_29+4836ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477457 | |||||
chr1:183477485
|
C | CGTGTGTG others(27): Show |
1 | a0001c0001t0004g0192 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.29+4869_29+4902dup others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477485 | |||||
chr1:183477485
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(318): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.29+4836C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477485 | ||||||
chr1:183477496
|
A | ATGTGTAT others(27): Show |
1 | a0001c0001t0003g0267 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.29+4880_29+4881ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477496 | |||||
chr1:183477519
|
T | TGTGTGTG others(25): Show |
18 | a0001c0001t0001g0018a0001c0001t0001g0102a0001c0001t0001g0105others(15): Show | 19 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.29+5041_29+5072dup others(32): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | |||||
chr1:183477519
|
T | TGTGTGTG others(59): Show |
5 | a0001c0001t0003g0203a0001c0001t0004g0200a0001c0001t0004g0201others(2): Show | 5 | HG00280.hp2 HG01070.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.29+4902_29+4903ins others(66): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | |||||
chr1:183477519
|
T | TGTGTGTG others(57): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0114 | 2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.29+5009_29+5072dup others(64): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | |||||
chr1:183477519
|
TGTGTGTG others(25): Show |
T | 6 | a0001c0001t0001g0173a0001c0001t0010g0186a0001c0001t0010g0187others(3): Show | 6 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.29+5041_29+5072del others(32): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | |||||
chr1:183477580
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(44): Show | 53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.29+4931A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477580 | ||||||
chr1:183477612
|
A | G | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | HG01123.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.29+4963A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477612 | ||||||
chr1:183477630
|
G | T | 2 | a0001c0001t0003g0246a0001c0001t0004g0247 | 2 | HG00558.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.29+4981G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477630 | ||||||
chr1:183477644
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.29+4995A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477644 | ||||||
chr1:183477655
|
CAT | C | 5 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0197others(2): Show | 5 | HG01257.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.29+5009_29+5010del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477655 | |||||
chr1:183477679
|
CGTGTGTG others(57): Show |
C | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.29+5047_29+5110del others(64): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477679 | |||||
chr1:183477712
|
G | GTGTGTGC others(25): Show |
1 | a0001c0001t0004g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.29+5072_29+5073ins others(32): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477712 | |||||
chr1:183477712
|
G | GTGTGTGC others(55): Show |
1 | a0002c0002t0012g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.29+5072_29+5073ins others(62): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477712 | |||||
chr1:183477719
|
C | CAT | 6 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+5071_29+5072dup others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477719 | |||||
chr1:183477719
|
C | CATATGTG others(59): Show |
1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.29+5072_29+5073ins others(66): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477719 | |||||
chr1:183477741
|
C | CGTGTGTG others(23): Show |
6 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+5092_29+5093ins others(30): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477741 | ||||||
chr1:183477742
|
A | G | 2 | a0001c0001t0001g0103a0003c0003t0001g0154 | 2 | HG02451.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.29+5093A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477742 | ||||||
chr1:183477743
|
T | C | 6 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+5094T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477743 | ||||||
chr1:183477776
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(324): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.29+5127G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477776 | ||||||
chr1:183477787
|
T | A | 103 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(100): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.29+5138T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477787 | ||||||
chr1:183477810
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.29+5161C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477810 | ||||||
chr1:183477810
|
CTA | C | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.29+5163_29+5164del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477810 | |||||
chr1:183477871
|
G | A | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+5222G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477871 | ||||||
chr1:183477885
|
G | T | 1 | a0002c0002t0005g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.29+5236G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477885 | ||||||
chr1:183478129
|
A | G | 1 | a0001c0001t0003g0266 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.29+5480A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478129 | ||||||
chr1:183478474
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0183 | 3 | HG01099.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29+5825G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478474 | ||||||
chr1:183478590
|
T | C | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+5941T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478590 | ||||||
chr1:183478593
|
G | A | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+5944G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478593 | ||||||
chr1:183478752
|
AT | A | 11 | a0001c0004t0001g0083a0001c0004t0001g0084a0001c0004t0001g0085others(8): Show | 11 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.29+6108delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183478752 | |||||
chr1:183478837
|
C | T | 1 | a0002c0002t0012g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.29+6188C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478837 | ||||||
chr1:183478889
|
A | G | 6 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+6240A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478889 | ||||||
chr1:183478975
|
T | C | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.29+6326T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478975 | ||||||
chr1:183479032
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.29+6383G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479032 | ||||||
chr1:183479039
|
C | G | 1 | a0001c0001t0004g0245 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.29+6390C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479039 | ||||||
chr1:183479288
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29+6639A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479288 | ||||||
chr1:183479429
|
G | A | 1 | a0002c0002t0002g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.29+6780G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479429 | ||||||
chr1:183479632
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.29+6983T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479632 | ||||||
chr1:183479981
|
T | C | 3 | a0001c0001t0006g0019a0001c0001t0009g0019a0001c0001t0009g0174 | 3 | HG02717.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.29+7332T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479981 | ||||||
chr1:183480193
|
G | A | 1 | a0002c0002t0002g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.29+7544G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480193 | ||||||
chr1:183480222
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(44): Show | 53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.29+7573C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480222 | ||||||
chr1:183480571
|
A | G | 1 | a0003c0003t0001g0017 | 2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.29+7922A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480571 | ||||||
chr1:183480658
|
A | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+8009A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480658 | ||||||
chr1:183480751
|
A | G | 1 | a0001c0001t0004g0265 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.29+8102A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480751 | ||||||
chr1:183480766
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(302): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.29+8117A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480766 | ||||||
chr1:183480779
|
A | G | 1 | a0002c0002t0002g0009 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.29+8130A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480779 | ||||||
chr1:183480849
|
T | C | 1 | a0001c0001t0006g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.29+8200T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480849 | ||||||
chr1:183481124
|
GGTATT | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+8478_29+8482del others(5): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481124 | |||||
chr1:183481172
|
G | T | 2 | a0001c0001t0003g0264a0001c0001t0007g0263 | 2 | NA18612.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.29+8523G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481172 | ||||||
chr1:183481487
|
G | C | 125 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(122): Show | 131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.29+8838G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481487 | ||||||
chr1:183481545
|
A | G | 1 | a0007c0007t0005g0172 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.29+8896A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481545 | ||||||
chr1:183481816
|
C | A | 57 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(54): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.29+9167C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481816 | ||||||
chr1:183481866
|
G | GCCCAGGC others(2792): Show |
2 | a0001c0001t0004g0193a0001c0001t0007g0194 | 2 | HG01257.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.29+9231_29+9232ins others(2799): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481866 | |||||
chr1:183481866
|
G | GCCCAGGC others(2793): Show |
2 | a0001c0001t0003g0195a0001c0001t0003g0196 | 2 | HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.29+9231_29+9232ins others(2800): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481866 | |||||
chr1:183481866
|
G | GCCCAGGC others(2794): Show |
1 | a0001c0001t0003g0197 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.29+9231_29+9232ins others(2801): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481866 | |||||
chr1:183482111
|
G | T | 1 | a0001c0001t0004g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.29+9462G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482111 | ||||||
chr1:183482212
|
A | T | 1 | a0002c0002t0002g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29+9563A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482212 | ||||||
chr1:183482230
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29+9581G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482230 | ||||||
chr1:183482390
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.29+9741A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482390 | ||||||
chr1:183482428
|
C | A | 4 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG01515.hp2 HG01517.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+9779C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482428 | ||||||
chr1:183482476
|
G | T | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.29+9827G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482476 | ||||||
chr1:183482630
|
C | T | 1 | a0002c0002t0002g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.29+9981C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482630 | ||||||
chr1:183482842
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29+10193G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482842 | ||||||
chr1:183482880
|
T | A | 2 | a0001c0001t0005g0095a0001c0001t0005g0096 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+10231T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482880 | ||||||
chr1:183482950
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.29+10301G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482950 | ||||||
chr1:183483410
|
G | A | 125 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(122): Show | 131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.29+10761G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183483410 | ||||||
chr1:183483523
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.29+10874C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183483523 | ||||||
chr1:183484049
|
G | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(324): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.29+11400G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484049 | ||||||
chr1:183484113
|
A | T | 1 | a0001c0001t0003g0260 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.29+11464A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484113 | ||||||
chr1:183484203
|
A | G | 1 | a0001c0001t0003g0024 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.29+11554A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484203 | ||||||
chr1:183484213
|
G | A | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+11564G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484213 | ||||||
chr1:183484360
|
A | AT | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0101others(49): Show | 58 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.29+11728dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183484360 | |||||
chr1:183484360
|
A | T | 122 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(119): Show | 128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.29+11711A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484360 | ||||||
chr1:183484389
|
G | T | 1 | a0001c0001t0001g0319 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.29+11740G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484389 | ||||||
chr1:183484417
|
G | A | 1 | a0001c0004t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.29+11768G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484417 | ||||||
chr1:183484760
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29+12111C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484760 | ||||||
chr1:183485053
|
A | G | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+12404A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183485053 | ||||||
chr1:183485835
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29+13186A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183485835 | ||||||
chr1:183486267
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.29+13618G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486267 | ||||||
chr1:183486316
|
G | A | 1 | a0003c0003t0001g0118 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.29+13667G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486316 | ||||||
chr1:183486423
|
T | G | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+13774T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486423 | ||||||
chr1:183486576
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0183 | 3 | HG01099.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29+13927G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486576 | ||||||
chr1:183486584
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.29+13935T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486584 | ||||||
chr1:183486689
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.29+14040G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486689 | ||||||
chr1:183486848
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29+14199C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486848 | ||||||
chr1:183486884
|
G | A | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+14235G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486884 | ||||||
chr1:183486999
|
C | T | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.29+14350C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486999 | ||||||
chr1:183487297
|
A | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+14648A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487297 | ||||||
chr1:183487341
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(42): Show | 51 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.29+14692C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487341 | ||||||
chr1:183487376
|
C | T | 1 | a0001c0001t0004g0243 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.29+14727C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487376 | ||||||
chr1:183487462
|
T | A | 1 | a0001c0010t0009g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.29+14813T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487462 | ||||||
chr1:183487610
|
C | T | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.29+14961C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487610 | ||||||
chr1:183487955
|
T | C | 1 | a0001c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.29+15306T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487955 | ||||||
chr1:183488063
|
A | G | 125 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(122): Show | 131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.29+15414A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488063 | ||||||
chr1:183488261
|
A | G | 113 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(110): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.29+15612A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488261 | ||||||
chr1:183488403
|
A | G | 1 | a0002c0002t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.29+15754A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488403 | ||||||
chr1:183488597
|
A | G | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.29+15948A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488597 | ||||||
chr1:183488682
|
C | CT | 23 | a0001c0001t0001g0112a0001c0001t0001g0151a0001c0001t0001g0283others(20): Show | 23 | HG01069.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.29+16056dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183488682 | |||||
chr1:183488682
|
CT | C | 195 | a0001c0001t0001g0018a0001c0001t0001g0102a0001c0001t0001g0103others(192): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.29+16056delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183488682 | |||||
chr1:183488684
|
T | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.29+16035T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488684 | ||||||
chr1:183488710
|
C | T | 1 | a0002c0002t0002g0011 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.29+16061C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488710 | ||||||
chr1:183488766
|
C | A | 1 | a0001c0001t0003g0203 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.29+16117C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488766 | ||||||
chr1:183488806
|
C | T | 1 | a0001c0001t0016g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29+16157C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488806 | ||||||
chr1:183488831
|
C | A | 1 | a0003c0003t0001g0147 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.29+16182C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488831 | ||||||
chr1:183488949
|
G | T | 1 | a0001c0004t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.29+16300G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488949 | ||||||
chr1:183489057
|
C | T | 1 | a0001c0001t0003g0203 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.29+16408C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489057 | ||||||
chr1:183489078
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.29+16429G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489078 | ||||||
chr1:183489094
|
A | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.29+16445A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489094 | ||||||
chr1:183489302
|
C | T | 1 | a0001c0001t0004g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.29+16653C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489302 | ||||||
chr1:183489324
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.29+16675G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489324 | ||||||
chr1:183489500
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.29+16851C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489500 | ||||||
chr1:183489508
|
T | C | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+16859T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489508 | ||||||
chr1:183489535
|
C | T | 1 | a0002c0002t0002g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.29+16886C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489535 | ||||||
chr1:183489583
|
A | G | 2 | a0001c0001t0001g0109a0002c0002t0002g0076 | 2 | HG02602.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.29+16934A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489583 | ||||||
chr1:183489657
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.29+17008A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489657 | ||||||
chr1:183489665
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.29+17016G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489665 | ||||||
chr1:183489822
|
A | G | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+17173A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489822 | ||||||
chr1:183489905
|
A | G | 1 | a0001c0001t0003g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29+17256A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489905 | ||||||
chr1:183490074
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.29+17425G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490074 | ||||||
chr1:183490177
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.29+17528A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490177 | ||||||
chr1:183490442
|
T | A | 1 | a0001c0001t0006g0251 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.29+17793T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490442 | ||||||
chr1:183490479
|
G | T | 1 | a0002c0002t0002g0076 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.29+17830G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490479 | ||||||
chr1:183490535
|
G | A | 112 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(109): Show | 116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.29+17886G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490535 | ||||||
chr1:183490825
|
G | A | 7 | a0002c0002t0002g0076a0003c0003t0001g0017a0003c0003t0001g0120others(4): Show | 8 | HG00423.hp1 HG01168.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.29+18176G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490825 | ||||||
chr1:183490911
|
A | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+18262A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490911 | ||||||
chr1:183491147
|
T | C | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.29+18498T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491147 | ||||||
chr1:183491194
|
G | A | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+18545G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491194 | ||||||
chr1:183491217
|
G | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.29+18568G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491217 | ||||||
chr1:183491391
|
G | T | 2 | a0006c0008t0001g0318a0006c0008t0001g0323 | 2 | HG01261.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.29+18742G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491391 | ||||||
chr1:183491435
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.29+18786G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491435 | ||||||
chr1:183491550
|
G | A | 1 | a0003c0003t0001g0154 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.29+18901G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491550 | ||||||
chr1:183491559
|
A | T | 1 | a0003c0003t0001g0146 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.29+18910A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491559 | ||||||
chr1:183491595
|
C | T | 1 | a0007c0007t0005g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.29+18946C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491595 | ||||||
chr1:183491983
|
G | C | 2 | a0002c0002t0002g0033a0002c0002t0002g0034 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.29+19334G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491983 | ||||||
chr1:183492136
|
A | G | 3 | a0001c0001t0006g0236a0001c0001t0006g0237a0001c0001t0006g0238 | 3 | NA18973.hp1 NA18998.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.29+19487A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492136 | ||||||
chr1:183492441
|
A | G | 1 | a0001c0001t0016g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29+19792A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492441 | ||||||
chr1:183492715
|
A | G | 1 | a0001c0001t0016g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29+20066A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492715 | ||||||
chr1:183492988
|
G | T | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-19849G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492988 | ||||||
chr1:183493149
|
C | CT | 113 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(110): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.30-19682dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183493149 | |||||
chr1:183493171
|
T | C | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-19666T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493171 | ||||||
chr1:183493177
|
A | G | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.30-19660A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493177 | ||||||
chr1:183493378
|
A | T | 126 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(123): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.30-19459A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493378 | ||||||
chr1:183493494
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.30-19343A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493494 | ||||||
chr1:183493601
|
A | T | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-19236A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493601 | ||||||
chr1:183493642
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30-19195C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493642 | ||||||
chr1:183493657
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0162 | 3 | HG02258.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.30-19180T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493657 | ||||||
chr1:183493749
|
T | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18970.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.30-19088T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493749 | ||||||
chr1:183493876
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01123.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.30-18961G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493876 | ||||||
chr1:183493999
|
C | T | 189 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(186): Show | 203 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.30-18838C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493999 | ||||||
chr1:183494136
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(42): Show | 51 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.30-18701C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494136 | ||||||
chr1:183494211
|
T | C | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-18626T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494211 | ||||||
chr1:183494277
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.30-18560C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494277 | ||||||
chr1:183494368
|
GT | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.30-18459delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494368 | |||||
chr1:183494472
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-18365G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494472 | ||||||
chr1:183494652
|
G | A | 305 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(302): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.30-18185G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494652 | ||||||
chr1:183494756
|
C | CT | 63 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0101others(60): Show | 69 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.30-18053dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | |||||
chr1:183494756
|
C | CTT | 14 | a0001c0001t0001g0152a0001c0001t0001g0311a0001c0001t0001g0317others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.30-18054_30-18053d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | |||||
chr1:183494756
|
CT | C | 147 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0003g0002others(144): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.30-18053delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | |||||
chr1:183494756
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG02647.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.30-18064_30-18053d others(14): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | |||||
chr1:183494789
|
TGGTGTCT others(56): Show |
T | 4 | a0002c0002t0002g0008a0002c0002t0002g0028a0002c0002t0002g0029others(1): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.30-17984_30-17922d others(65): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494789 | |||||
chr1:183494987
|
C | T | 1 | a0005c0006t0001g0309 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.30-17850C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494987 | ||||||
chr1:183495079
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.30-17758G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495079 | ||||||
chr1:183495157
|
A | G | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.30-17680A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495157 | ||||||
chr1:183495193
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(324): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.30-17644G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495193 | ||||||
chr1:183495229
|
T | C | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.30-17608T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495229 | ||||||
chr1:183495268
|
G | A | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-17569G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495268 | ||||||
chr1:183495454
|
A | G | 1 | a0002c0002t0002g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.30-17383A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495454 | ||||||
chr1:183495489
|
G | A | 1 | a0001c0001t0003g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.30-17348G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495489 | ||||||
chr1:183495583
|
A | C | 1 | a0002c0002t0002g0039 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30-17254A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495583 | ||||||
chr1:183495596
|
C | T | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-17241C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495596 | ||||||
chr1:183495804
|
G | T | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.30-17033G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495804 | ||||||
chr1:183495872
|
A | G | 1 | a0001c0001t0007g0194 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.30-16965A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495872 | ||||||
chr1:183495909
|
T | C | 1 | a0002c0002t0002g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30-16928T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495909 | ||||||
chr1:183496543
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0319 | 2 | HG01099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.30-16294G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496543 | ||||||
chr1:183496546
|
A | G | 1 | a0001c0001t0016g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.30-16291A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496546 | ||||||
chr1:183496672
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30-16165T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496672 | ||||||
chr1:183496806
|
A | G | 3 | a0003c0003t0001g0016a0003c0003t0001g0139a0003c0003t0001g0145 | 4 | HG00597.hp1 NA18939.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-16031A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496806 | ||||||
chr1:183497150
|
A | G | 17 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0044others(14): Show | 20 | HG00558.hp2 HG00609.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.30-15687A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497150 | ||||||
chr1:183497170
|
T | C | 42 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0010others(39): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.30-15667T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497170 | ||||||
chr1:183497494
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.30-15343T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497494 | ||||||
chr1:183497673
|
G | A | 1 | a0001c0001t0015g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30-15164G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497673 | ||||||
chr1:183497724
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30-15113C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497724 | ||||||
chr1:183497725
|
G | A | 1 | a0004c0005t0005g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.30-15112G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497725 | ||||||
chr1:183497776
|
G | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-15061G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497776 | ||||||
chr1:183497833
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0128 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.30-15004G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497833 | ||||||
chr1:183497960
|
G | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0112a0001c0001t0001g0113others(5): Show | 9 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.30-14877G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497960 | ||||||
chr1:183498175
|
A | G | 1 | a0001c0001t0005g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.30-14662A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498175 | ||||||
chr1:183498374
|
C | A | 1 | a0007c0007t0005g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30-14463C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498374 | ||||||
chr1:183498437
|
G | A | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.30-14400G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498437 | ||||||
chr1:183498534
|
T | C | 2 | a0001c0001t0004g0206a0001c0001t0004g0207 | 2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.30-14303T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498534 | ||||||
chr1:183498618
|
A | G | 1 | a0003c0003t0001g0123 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.30-14219A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498618 | ||||||
chr1:183498767
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30-14070C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498767 | ||||||
chr1:183499007
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30-13830A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499007 | ||||||
chr1:183499120
|
G | C | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-13717G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499120 | ||||||
chr1:183499172
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.30-13665T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499172 | ||||||
chr1:183499285
|
T | G | 42 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0010others(39): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.30-13552T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499285 | ||||||
chr1:183499400
|
T | C | 2 | a0001c0001t0003g0230a0001c0001t0006g0208 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.30-13437T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499400 | ||||||
chr1:183499405
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.30-13432A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499405 | ||||||
chr1:183499737
|
C | A | 1 | a0001c0001t0001g0294 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.30-13100C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499737 | ||||||
chr1:183500036
|
G | C | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-12801G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500036 | ||||||
chr1:183500551
|
A | G | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30-12286A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500551 | ||||||
chr1:183500791
|
G | T | 2 | a0002c0002t0002g0028a0002c0002t0002g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30-12046G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500791 | ||||||
chr1:183500968
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30-11869A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500968 | ||||||
chr1:183500974
|
G | T | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-11863G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500974 | ||||||
chr1:183500981
|
G | T | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-11856G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500981 | ||||||
chr1:183501048
|
A | G | 2 | a0002c0002t0002g0027a0002c0002t0002g0037 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.30-11789A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501048 | ||||||
chr1:183501112
|
A | C | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.30-11725A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501112 | ||||||
chr1:183501377
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30-11460C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501377 | ||||||
chr1:183501462
|
C | T | 2 | a0002c0002t0002g0027a0002c0002t0002g0037 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.30-11375C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501462 | ||||||
chr1:183501890
|
A | G | 5 | a0001c0001t0003g0259a0001c0001t0003g0270a0001c0001t0003g0271others(2): Show | 5 | HG00544.hp1 NA18971.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.30-10947A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501890 | ||||||
chr1:183502160
|
G | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(316): Show | 346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.30-10677G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183502160 | ||||||
chr1:183503287
|
T | C | 1 | a0001c0001t0004g0265 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.30-9550T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503287 | ||||||
chr1:183503390
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.30-9447C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503390 | ||||||
chr1:183503538
|
T | A | 1 | a0002c0002t0002g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.30-9299T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503538 | ||||||
chr1:183503671
|
A | G | 2 | a0002c0002t0002g0072a0002c0002t0002g0073 | 2 | NA18998.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.30-9166A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503671 | ||||||
chr1:183503742
|
C | A | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.30-9095C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503742 | ||||||
chr1:183503778
|
G | T | 2 | a0001c0001t0003g0270a0001c0001t0003g0271 | 2 | NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.30-9059G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503778 | ||||||
chr1:183503937
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.30-8900A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503937 | ||||||
chr1:183503970
|
C | G | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.30-8867C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503970 | ||||||
chr1:183504103
|
A | G | 5 | a0002c0002t0002g0008a0002c0002t0002g0028a0002c0002t0002g0029others(2): Show | 6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.30-8734A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504103 | ||||||
chr1:183504233
|
A | G | 1 | a0001c0001t0003g0023 | 2 | NA18943.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.30-8604A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504233 | ||||||
chr1:183504286
|
T | C | 1 | a0001c0001t0003g0203 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.30-8551T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504286 | ||||||
chr1:183504304
|
G | A | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.30-8533G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504304 | ||||||
chr1:183504324
|
G | GATTT | 18 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(15): Show | 19 | HG01099.hp2 HG01167.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.30-8484_30-8481dup others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183504324 | |||||
chr1:183504324
|
G | GATTTATT others(1): Show |
4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-8488_30-8481dup others(8): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183504324 | |||||
chr1:183504324
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0016g0180 | 2 | HG01099.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.30-8513G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504324 | ||||||
chr1:183504324
|
GATTTATT others(5): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.30-8492_30-8481del others(12): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183504324 | |||||
chr1:183504501
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30-8336C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504501 | ||||||
chr1:183504513
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30-8324A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504513 | ||||||
chr1:183504629
|
G | A | 2 | a0002c0002t0002g0028a0002c0002t0002g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30-8208G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504629 | ||||||
chr1:183504763
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.30-8074C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504763 | ||||||
chr1:183504775
|
C | T | 1 | a0001c0001t0007g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30-8062C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504775 | ||||||
chr1:183504931
|
C | T | 1 | a0002c0002t0008g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.30-7906C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504931 | ||||||
chr1:183505147
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.30-7690G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505147 | ||||||
chr1:183505224
|
C | A | 1 | a0001c0001t0004g0247 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.30-7613C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505224 | ||||||
chr1:183505266
|
A | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-7571A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505266 | ||||||
chr1:183505552
|
C | G | 1 | a0007c0007t0005g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30-7285C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505552 | ||||||
chr1:183505559
|
C | T | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-7278C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505559 | ||||||
chr1:183505626
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30-7211C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505626 | ||||||
chr1:183505711
|
C | G | 1 | a0001c0004t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30-7126C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505711 | ||||||
chr1:183505715
|
G | C | 113 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(110): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.30-7122G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505715 | ||||||
chr1:183505783
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.30-7054G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505783 | ||||||
chr1:183505852
|
G | GT | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-6980dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183505852 | |||||
chr1:183505895
|
A | C | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-6942A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505895 | ||||||
chr1:183506101
|
G | A | 2 | a0001c0004t0001g0091a0001c0004t0001g0092 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.30-6736G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506101 | ||||||
chr1:183506288
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.30-6549C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506288 | ||||||
chr1:183506395
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30-6442T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506395 | ||||||
chr1:183506602
|
A | G | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.30-6235A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506602 | ||||||
chr1:183506653
|
T | TA | 63 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(60): Show | 68 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.30-6170dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506653 | |||||
chr1:183506653
|
TA | T | 6 | a0001c0001t0001g0313a0001c0001t0003g0195a0001c0001t0004g0245others(3): Show | 6 | HG01081.hp2 HG01975.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-6170delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506653 | |||||
chr1:183506670
|
C | T | 1 | a0007c0007t0005g0172 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.30-6167C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506670 | ||||||
chr1:183506706
|
A | C | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-6131A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506706 | ||||||
chr1:183506875
|
C | CT | 120 | a0001c0001t0001g0117a0001c0001t0001g0156a0001c0001t0001g0173others(117): Show | 125 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.30-5942dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506875 | |||||
chr1:183506875
|
CT | C | 6 | a0001c0001t0005g0095a0002c0002t0002g0027a0002c0002t0002g0031others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.30-5942delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506875 | |||||
chr1:183507036
|
G | A | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-5801G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507036 | ||||||
chr1:183507254
|
C | G | 2 | a0003c0003t0001g0118a0003c0003t0001g0137 | 2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.30-5583C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507254 | ||||||
chr1:183507483
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30-5354C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507483 | ||||||
chr1:183507563
|
A | G | 1 | a0001c0004t0001g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.30-5274A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507563 | ||||||
chr1:183507794
|
G | A | 112 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(109): Show | 116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.30-5043G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507794 | ||||||
chr1:183507953
|
C | T | 1 | a0002c0002t0002g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30-4884C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507953 | ||||||
chr1:183508059
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30-4778T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508059 | ||||||
chr1:183508096
|
G | A | 256 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0112others(253): Show | 276 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.30-4741G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508096 | ||||||
chr1:183508110
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-4727G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508110 | ||||||
chr1:183508389
|
T | G | 5 | a0002c0002t0002g0046a0002c0002t0002g0047a0002c0002t0002g0053others(2): Show | 5 | NA18960.hp1 NA18978.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.30-4448T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508389 | ||||||
chr1:183508457
|
A | C | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-4380A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508457 | ||||||
chr1:183508483
|
T | C | 1 | a0002c0002t0002g0046 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.30-4354T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508483 | ||||||
chr1:183508517
|
A | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG00099.hp2 HG01070.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.30-4320A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508517 | ||||||
chr1:183508912
|
T | G | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30-3925T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508912 | ||||||
chr1:183509160
|
A | G | 6 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(3): Show | 7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.30-3677A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509160 | ||||||
chr1:183509328
|
G | T | 54 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0124others(51): Show | 59 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.30-3509G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509328 | ||||||
chr1:183509524
|
G | A | 1 | a0001c0001t0003g0024 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.30-3313G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509524 | ||||||
chr1:183509562
|
C | A | 2 | a0002c0002t0002g0027a0002c0002t0002g0037 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.30-3275C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509562 | ||||||
chr1:183509586
|
A | G | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.30-3251A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509586 | ||||||
chr1:183509847
|
A | T | 1 | a0001c0001t0003g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30-2990A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509847 | ||||||
chr1:183509951
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30-2886A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509951 | ||||||
chr1:183509955
|
T | C | 125 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(122): Show | 131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.30-2882T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509955 | ||||||
chr1:183509967
|
A | G | 1 | a0001c0010t0009g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.30-2870A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509967 | ||||||
chr1:183510151
|
G | A | 1 | a0001c0001t0006g0211 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.30-2686G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510151 | ||||||
chr1:183510228
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30-2609A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510228 | ||||||
chr1:183510307
|
C | T | 9 | a0001c0001t0003g0226a0001c0001t0003g0252a0001c0001t0003g0257others(6): Show | 9 | HG01106.hp2 HG01192.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.30-2530C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510307 | ||||||
chr1:183510471
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.30-2366G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510471 | ||||||
chr1:183510860
|
A | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-1977A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510860 | ||||||
chr1:183511129
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30-1708T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511129 | ||||||
chr1:183511304
|
T | C | 1 | a0001c0001t0003g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30-1533T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511304 | ||||||
chr1:183511576
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30-1261G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511576 | ||||||
chr1:183511967
|
C | A | 64 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(61): Show | 72 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.30-870C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511967 | ||||||
chr1:183512203
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-634G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183512203 | ||||||
chr1:183512655
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30-182C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183512655 | ||||||
chr1:183512808
|
C | CT | 108 | a0001c0001t0001g0307a0001c0001t0003g0002a0001c0001t0003g0006others(105): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
splice_region_variant&intron_variant | LOW | c.30-9dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183512808 | |||||
chr1:183512808
|
CT | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0112a0001c0001t0001g0113others(9): Show | 13 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.30-9delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183512808 | |||||
chr1:183512950
|
A | G | 1 | a0001c0001t0004g0247 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.61+82A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183512950 | ||||||
chr1:183512974
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.61+106G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183512974 | ||||||
chr1:183513060
|
G | A | 3 | a0001c0004t0001g0083a0001c0004t0001g0086a0001c0004t0001g0090 | 3 | HG00280.hp2 HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.61+192G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513060 | ||||||
chr1:183513369
|
C | CT | 10 | a0001c0001t0001g0018a0001c0001t0001g0105a0001c0001t0001g0162others(7): Show | 11 | HG01192.hp2 HG01516.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+521dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513369 | |||||
chr1:183513369
|
C | CTT | 57 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(54): Show | 65 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.61+520_61+521dupTT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513369 | |||||
chr1:183513369
|
CT | C | 8 | a0001c0001t0003g0178a0001c0001t0003g0244a0001c0001t0004g0231others(5): Show | 8 | HG01891.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+521delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513369 | |||||
chr1:183513433
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61+565G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513433 | ||||||
chr1:183513465
|
T | C | 3 | a0002c0002t0002g0063a0002c0002t0002g0070a0002c0002t0002g0078 | 3 | HG01257.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.61+597T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513465 | ||||||
chr1:183513520
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0128 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.61+652C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513520 | ||||||
chr1:183513577
|
G | C | 1 | a0001c0001t0011g0273 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.61+709G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513577 | ||||||
chr1:183513650
|
G | A | 61 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(58): Show | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.61+782G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513650 | ||||||
chr1:183513717
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.61+849G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513717 | ||||||
chr1:183513756
|
G | T | 1 | a0001c0001t0017g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.61+888G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513756 | ||||||
chr1:183513758
|
G | A | 2 | a0002c0002t0002g0042a0002c0002t0005g0043 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.61+890G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513758 | ||||||
chr1:183513768
|
G | C | 1 | a0004c0005t0005g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.61+900G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513768 | ||||||
chr1:183513875
|
C | G | 1 | a0003c0003t0001g0136 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.61+1007C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513875 | ||||||
chr1:183513880
|
AT | A | 9 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0044others(6): Show | 12 | HG00558.hp2 HG02129.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+1014delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513880 | |||||
chr1:183514029
|
C | CA | 17 | a0001c0001t0001g0021a0001c0001t0001g0101a0001c0001t0001g0158others(14): Show | 18 | HG00438.hp1 HG00438.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+1182dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514029 | |||||
chr1:183514029
|
CA | C | 20 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(17): Show | 21 | HG01070.hp1 HG01070.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.61+1182delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514029 | |||||
chr1:183514029
|
CAA | C | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+1181_61+1182del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514029 | |||||
chr1:183514044
|
A | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0195a0001c0001t0003g0196others(9): Show | 13 | HG01257.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+1176A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514044 | ||||||
chr1:183514095
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.61+1227C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514095 | ||||||
chr1:183514119
|
C | T | 1 | a0002c0002t0002g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.61+1251C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514119 | ||||||
chr1:183514216
|
C | CA | 52 | a0001c0001t0001g0082a0001c0001t0001g0115a0001c0001t0001g0116others(49): Show | 58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.61+1365dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514216 | |||||
chr1:183514216
|
C | CAAA | 7 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0140others(4): Show | 7 | HG01433.hp2 HG01978.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+1363_61+1365dup others(3): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514216 | |||||
chr1:183514216
|
CA | C | 83 | a0001c0001t0001g0107a0001c0001t0001g0294a0001c0001t0003g0178others(80): Show | 94 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.61+1365delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514216 | |||||
chr1:183514643
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.62-1231C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514643 | ||||||
chr1:183514780
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.62-1094G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514780 | ||||||
chr1:183515038
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-836G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515038 | ||||||
chr1:183515048
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.62-826T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515048 | ||||||
chr1:183515106
|
T | G | 2 | a0001c0001t0005g0095a0001c0001t0005g0096 | 2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.62-768T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515106 | ||||||
chr1:183515132
|
T | C | 1 | a0002c0002t0002g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-742T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515132 | ||||||
chr1:183515145
|
C | G | 1 | a0002c0002t0002g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-729C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515145 | ||||||
chr1:183515161
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.62-713G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515161 | ||||||
chr1:183515162
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.62-712A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515162 | ||||||
chr1:183515195
|
C | A | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.62-679C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515195 | ||||||
chr1:183515270
|
CTT | C | 42 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0010others(39): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.62-603_62-602delTT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515270 | ||||||
chr1:183515288
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.62-586G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515288 | ||||||
chr1:183515527
|
T | C | 1 | a0001c0001t0016g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-347T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515527 | ||||||
chr1:183515605
|
C | CT | 64 | a0001c0001t0001g0151a0001c0001t0003g0256a0001c0001t0003g0270others(61): Show | 71 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.62-251dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183515605 | |||||
chr1:183515605
|
CT | C | 11 | a0001c0001t0001g0173a0001c0001t0001g0286a0001c0001t0004g0200others(8): Show | 11 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-251delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183515605 | |||||
chr1:183515676
|
A | AACCAGAC | 17 | a0003c0003t0001g0012a0003c0003t0001g0013a0003c0003t0001g0017others(14): Show | 20 | HG00408.hp1 HG00423.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.62-197_62-191dupAC others(5): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183515676 | |||||
chr1:183515851
|
A | G | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.62-23A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515851 | ||||||
chr1:183516224
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.179+233G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516224 | ||||||
chr1:183516259
|
C | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.179+268C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516259 | ||||||
chr1:183516314
|
C | A | 2 | a0001c0001t0014g0157a0001c0001t0018g0181 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.179+323C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516314 | ||||||
chr1:183516482
|
A | G | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.179+491A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516482 | ||||||
chr1:183516758
|
C | T | 1 | a0002c0002t0002g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.179+767C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516758 | ||||||
chr1:183516819
|
T | G | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.179+828T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516819 | ||||||
chr1:183516890
|
A | G | 1 | a0002c0002t0002g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.180-798A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516890 | ||||||
chr1:183516908
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.180-780A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516908 | ||||||
chr1:183516969
|
A | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-719A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516969 | ||||||
chr1:183517253
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.180-435G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517253 | ||||||
chr1:183517285
|
C | T | 1 | a0007c0007t0005g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.180-403C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517285 | ||||||
chr1:183517480
|
T | C | 1 | a0002c0002t0002g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.180-208T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517480 | ||||||
chr1:183517499
|
G | T | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.180-189G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517499 | ||||||
chr1:183517523
|
T | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG02647.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.180-165T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517523 | ||||||
chr1:183517919
|
A | G | 2 | a0001c0001t0004g0176a0001c0001t0007g0175 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312+99A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183517919 | ||||||
chr1:183517929
|
T | A | 1 | a0003c0003t0001g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.312+109T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183517929 | ||||||
chr1:183517948
|
T | C | 1 | a0004c0005t0005g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.312+128T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183517948 | ||||||
chr1:183518002
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.312+182T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518002 | ||||||
chr1:183518129
|
G | A | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+309G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518129 | ||||||
chr1:183518173
|
C | T | 1 | a0001c0001t0014g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.312+353C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518173 | ||||||
chr1:183518261
|
C | T | 1 | a0003c0003t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.312+441C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518261 | ||||||
chr1:183518270
|
A | G | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0304 | 3 | NA18970.hp2 NA18992.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.312+450A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518270 | ||||||
chr1:183518445
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.312+625C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518445 | ||||||
chr1:183518445
|
CTA | C | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+628_312+629del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183518445 | |||||
chr1:183518714
|
A | G | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.312+894A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518714 | ||||||
chr1:183518836
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.312+1016T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518836 | ||||||
chr1:183518909
|
A | G | 1 | a0001c0004t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.312+1089A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518909 | ||||||
chr1:183519246
|
A | G | 1 | a0001c0001t0004g0225 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.312+1426A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519246 | ||||||
chr1:183519356
|
C | T | 2 | a0003c0003t0001g0134a0003c0003t0001g0155 | 2 | NA18943.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.312+1536C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519356 | ||||||
chr1:183519392
|
C | T | 58 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(55): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.312+1572C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519392 | ||||||
chr1:183519780
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.312+1960G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519780 | ||||||
chr1:183520025
|
A | AT | 40 | a0001c0001t0019g0184a0002c0002t0002g0077a0003c0003t0001g0012others(37): Show | 45 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.312+2218dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183520025 | |||||
chr1:183520068
|
G | A | 111 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(108): Show | 115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.312+2248G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520068 | ||||||
chr1:183520143
|
G | A | 111 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(108): Show | 115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.312+2323G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520143 | ||||||
chr1:183520164
|
C | A | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.312+2344C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520164 | ||||||
chr1:183520547
|
A | C | 1 | a0002c0002t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.312+2727A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520547 | ||||||
chr1:183520862
|
G | C | 2 | a0001c0001t0003g0203a0001c0001t0004g0202 | 2 | NA18946.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.312+3042G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520862 | ||||||
chr1:183520911
|
G | C | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.312+3091G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520911 | ||||||
chr1:183521004
|
G | A | 1 | a0001c0001t0003g0260 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.312+3184G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521004 | ||||||
chr1:183521015
|
C | T | 2 | a0001c0001t0004g0231a0008c0009t0007g0198 | 2 | HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.312+3195C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521015 | ||||||
chr1:183521072
|
C | CT | 8 | a0001c0001t0001g0292a0001c0001t0003g0203a0001c0001t0006g0211others(5): Show | 8 | HG04228.hp1 NA18906.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+3270dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183521072 | |||||
chr1:183521072
|
CT | C | 13 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(10): Show | 13 | HG02027.hp1 HG02056.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.312+3270delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183521072 | |||||
chr1:183521168
|
C | T | 2 | a0001c0001t0014g0157a0001c0001t0018g0181 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+3348C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521168 | ||||||
chr1:183521327
|
G | C | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.312+3507G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521327 | ||||||
chr1:183521481
|
C | G | 58 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(55): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.312+3661C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521481 | ||||||
chr1:183521495
|
G | T | 1 | a0001c0001t0006g0190 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.312+3675G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521495 | ||||||
chr1:183521562
|
G | A | 1 | a0001c0001t0007g0240 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.312+3742G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521562 | ||||||
chr1:183521681
|
C | T | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.312+3861C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521681 | ||||||
chr1:183521858
|
C | CA | 242 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(239): Show | 260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.312+4054dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183521858 | |||||
chr1:183521875
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.312+4055G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521875 | ||||||
chr1:183521878
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.312+4058G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521878 | ||||||
chr1:183522030
|
A | G | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.312+4210A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522030 | ||||||
chr1:183522256
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.313-4340A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522256 | ||||||
chr1:183522268
|
T | G | 2 | a0001c0001t0003g0280a0001c0001t0004g0274 | 2 | NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.313-4328T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522268 | ||||||
chr1:183522271
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313-4325T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522271 | ||||||
chr1:183523070
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313-3526A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523070 | ||||||
chr1:183523072
|
A | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-3524A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523072 | ||||||
chr1:183523117
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.313-3479G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523117 | ||||||
chr1:183523417
|
A | G | 1 | a0001c0004t0001g0093 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.313-3179A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523417 | ||||||
chr1:183523771
|
T | A | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.313-2825T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523771 | ||||||
chr1:183523786
|
T | C | 1 | a0001c0001t0009g0232 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.313-2810T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523786 | ||||||
chr1:183523864
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.313-2732A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523864 | ||||||
chr1:183523874
|
G | T | 1 | a0001c0001t0005g0224 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.313-2722G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523874 | ||||||
chr1:183523897
|
A | G | 1 | a0007c0007t0005g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.313-2699A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523897 | ||||||
chr1:183523977
|
T | A | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-2619T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523977 | ||||||
chr1:183524086
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-2510T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524086 | ||||||
chr1:183524198
|
C | T | 2 | a0003c0003t0001g0133a0003c0003t0001g0144 | 2 | NA18947.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.313-2398C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524198 | ||||||
chr1:183524251
|
T | G | 1 | a0001c0001t0018g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.313-2345T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524251 | ||||||
chr1:183524401
|
A | G | 1 | a0003c0003t0001g0182 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.313-2195A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524401 | ||||||
chr1:183524681
|
C | T | 2 | a0003c0003t0001g0015a0003c0003t0001g0131 | 3 | NA18948.hp1 NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.313-1915C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524681 | ||||||
chr1:183524827
|
C | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-1769C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524827 | ||||||
chr1:183525079
|
A | G | 113 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(110): Show | 117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.313-1517A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525079 | ||||||
chr1:183525119
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.313-1477A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525119 | ||||||
chr1:183525134
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-1462G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525134 | ||||||
chr1:183525200
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.313-1396C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525200 | ||||||
chr1:183525285
|
G | T | 9 | a0003c0003t0001g0013a0003c0003t0001g0017a0003c0003t0001g0120others(6): Show | 11 | HG00423.hp1 HG01168.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.313-1311G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525285 | ||||||
chr1:183525318
|
G | A | 190 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(187): Show | 204 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.313-1278G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525318 | ||||||
chr1:183525391
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(316): Show | 346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.313-1205A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525391 | ||||||
chr1:183525409
|
G | A | 1 | a0001c0001t0005g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.313-1187G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525409 | ||||||
chr1:183525813
|
T | C | 1 | a0001c0001t0004g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.313-783T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525813 | ||||||
chr1:183525884
|
T | C | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-712T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525884 | ||||||
chr1:183525885
|
C | T | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-711C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525885 | ||||||
chr1:183525932
|
T | G | 1 | a0002c0002t0008g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.313-664T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525932 | ||||||
chr1:183525968
|
TTTGC | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG02647.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.313-621_313-618del others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183525968 | |||||
chr1:183525999
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-597C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525999 | ||||||
chr1:183526153
|
TA | T | 4 | a0001c0001t0001g0105a0001c0001t0003g0230a0001c0001t0006g0208others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-442delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526153 | ||||||
chr1:183526154
|
A | T | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-442A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526154 | ||||||
chr1:183526155
|
TA | T | 186 | a0001c0001t0001g0021a0001c0001t0001g0082a0001c0001t0001g0102others(183): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.313-440delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526155 | ||||||
chr1:183526156
|
A | AT | 6 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-429dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183526156 | |||||
chr1:183526156
|
A | ATTT | 55 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0008others(52): Show | 63 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.313-431_313-429dup others(3): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183526156 | |||||
chr1:183526156
|
A | T | 8 | a0001c0001t0001g0105a0001c0001t0003g0230a0001c0001t0006g0208others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-440A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526156 | ||||||
chr1:183526156
|
AT | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(44): Show | 53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.313-429delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183526156 | |||||
chr1:183526159
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0294 | 4 | HG03654.hp1 NA18946.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-437T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526159 | ||||||
chr1:183526278
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0277 | 2 | HG02056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.313-318A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526278 | ||||||
chr1:183526311
|
G | C | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-285G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526311 | ||||||
chr1:183526312
|
C | G | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-284C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526312 | ||||||
chr1:183526397
|
G | A | 1 | a0001c0001t0018g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.313-199G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526397 | ||||||
chr1:183526496
|
T | G | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-100T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526496 | ||||||
chr1:183526531
|
G | A | 1 | a0002c0002t0008g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.313-65G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526531 | ||||||
chr1:183526539
|
A | C | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-57A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526539 | ||||||
chr1:183526540
|
C | T | 1 | a0010c0013t0001g0296 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-56C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526540 | ||||||
chr1:183526548
|
T | G | 1 | a0003c0003t0001g0017 | 2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.313-48T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526548 | ||||||
chr1:183526578
|
T | C | 9 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(6): Show | 10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-18T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526578 | ||||||
chr1:183527235
|
G | A | 1 | a0002c0002t0002g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.484+468G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527235 | ||||||
chr1:183527246
|
A | T | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.484+479A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527246 | ||||||
chr1:183527523
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(42): Show | 51 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.485-433A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527523 | ||||||
chr1:183527854
|
A | G | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.485-102A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527854 | ||||||
chr1:183528492
|
G | A | 57 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(54): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.557-400G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528492 | ||||||
chr1:183528553
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.557-339C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528553 | ||||||
chr1:183528672
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.557-220G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528672 | ||||||
chr1:183528724
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.557-168C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528724 | ||||||
chr1:183529183
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0003g0191 | 2 | HG03516.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.707+141A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 7/22 | chr1 | 183529183 | ||||||
chr1:183530013
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.843+480C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530013 | ||||||
chr1:183530028
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.843+495T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530028 | ||||||
chr1:183530129
|
A | T | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.843+596A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530129 | ||||||
chr1:183530159
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843+626C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530159 | ||||||
chr1:183530389
|
C | T | 2 | a0002c0002t0002g0033a0002c0002t0002g0034 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.843+856C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530389 | ||||||
chr1:183530424
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.843+891T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530424 | ||||||
chr1:183530514
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.843+981A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530514 | ||||||
chr1:183530696
|
C | T | 1 | a0006c0008t0001g0318 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.843+1163C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530696 | ||||||
chr1:183530697
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.843+1164G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530697 | ||||||
chr1:183530975
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.843+1442A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530975 | ||||||
chr1:183531025
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.843+1492T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531025 | ||||||
chr1:183531044
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.843+1511C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531044 | ||||||
chr1:183531212
|
T | G | 2 | a0002c0002t0002g0042a0002c0002t0005g0043 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.843+1679T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531212 | ||||||
chr1:183531235
|
G | T | 1 | a0001c0001t0015g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.843+1702G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531235 | ||||||
chr1:183531270
|
A | G | 1 | a0002c0002t0002g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.843+1737A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531270 | ||||||
chr1:183531445
|
C | T | 1 | a0002c0002t0002g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.844-1719C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531445 | ||||||
chr1:183531814
|
A | G | 1 | a0002c0002t0002g0066 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.844-1350A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531814 | ||||||
chr1:183531834
|
G | A | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1330G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531834 | ||||||
chr1:183531835
|
C | T | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1329C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531835 | ||||||
chr1:183532104
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.844-1060G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532104 | ||||||
chr1:183532187
|
G | A | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-977G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532187 | ||||||
chr1:183532215
|
C | T | 3 | a0001c0001t0004g0192a0001c0001t0006g0204a0001c0001t0007g0222 | 3 | HG01256.hp1 HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844-949C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532215 | ||||||
chr1:183532316
|
G | T | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0096 | 3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.844-848G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532316 | ||||||
chr1:183532355
|
T | G | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.844-809T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532355 | ||||||
chr1:183532526
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.844-638C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532526 | ||||||
chr1:183532639
|
A | C | 41 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0024others(38): Show | 43 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.844-525A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532639 | ||||||
chr1:183532845
|
G | A | 2 | a0001c0001t0004g0201a0001c0001t0007g0241 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.844-319G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532845 | ||||||
chr1:183532995
|
G | A | 1 | a0001c0004t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.844-169G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532995 | ||||||
chr1:183533060
|
A | G | 1 | a0001c0001t0004g0225 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.844-104A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183533060 | ||||||
chr1:183533098
|
AT | A | 65 | a0001c0001t0006g0237a0001c0001t0010g0186a0001c0001t0010g0187others(62): Show | 73 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.844-63delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 183533098 | |||||
chr1:183533486
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1006+160T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 9/22 | chr1 | 183533486 | ||||||
chr1:183533596
|
G | C | 1 | a0002c0002t0012g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1007-80G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 9/22 | chr1 | 183533596 | ||||||
chr1:183533928
|
C | A | 5 | a0002c0002t0002g0046a0002c0002t0002g0047a0002c0002t0002g0053others(2): Show | 5 | NA18960.hp1 NA18978.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163+96C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183533928 | ||||||
chr1:183534043
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1163+211A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534043 | ||||||
chr1:183534138
|
T | C | 3 | a0001c0001t0006g0019a0001c0001t0009g0019a0001c0001t0009g0174 | 3 | HG02717.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1163+306T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534138 | ||||||
chr1:183534177
|
A | AG | 59 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(56): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1163+348dupG | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 183534177 | |||||
chr1:183534302
|
A | G | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1163+470A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534302 | ||||||
chr1:183534367
|
A | G | 1 | a0001c0004t0001g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1163+535A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534367 | ||||||
chr1:183534529
|
A | G | 37 | a0001c0001t0003g0023a0001c0001t0003g0203a0001c0001t0003g0209others(34): Show | 38 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1163+697A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534529 | ||||||
chr1:183534800
|
G | C | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1163+968G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534800 | ||||||
chr1:183534803
|
G | A | 39 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0024others(36): Show | 41 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1163+971G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534803 | ||||||
chr1:183534807
|
C | T | 9 | a0001c0001t0003g0178a0001c0001t0004g0176a0001c0001t0004g0179others(6): Show | 10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163+975C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534807 | ||||||
chr1:183534823
|
C | T | 4 | a0001c0001t0003g0221a0001c0001t0004g0239a0001c0001t0004g0258others(1): Show | 4 | NA18960.hp2 NA19012.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163+991C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534823 | ||||||
chr1:183535013
|
G | T | 1 | a0001c0001t0021g0287 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1163+1181G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535013 | ||||||
chr1:183535020
|
G | A | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1163+1188G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535020 | ||||||
chr1:183535126
|
ATATAT | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0291a0001c0001t0001g0292others(9): Show | 16 | HG02523.hp1 NA18953.hp2 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1163+1300_1163+130 others(9): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 183535126 | |||||
chr1:183535236
|
T | G | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163+1404T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535236 | ||||||
chr1:183535750
|
T | C | 59 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(56): Show | 64 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1164-1395T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535750 | ||||||
chr1:183535811
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1164-1334G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535811 | ||||||
chr1:183535862
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1164-1283T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535862 | ||||||
chr1:183535909
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1164-1236C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535909 | ||||||
chr1:183536102
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1164-1043T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183536102 | ||||||
chr1:183536121
|
T | C | 3 | a0001c0001t0001g0300a0001c0001t0001g0308a0001c0001t0001g0312 | 3 | HG00544.hp2 NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1164-1024T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183536121 | ||||||
chr1:183536210
|
A | T | 1 | a0001c0001t0001g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1164-935A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183536210 | ||||||
chr1:183537707
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234+492A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537707 | ||||||
chr1:183537944
|
A | G | 2 | a0001c0001t0014g0157a0001c0001t0018g0181 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1235-436A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537944 | ||||||
chr1:183537945
|
A | G | 1 | a0002c0002t0012g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1235-435A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537945 | ||||||
chr1:183537970
|
G | A | 10 | a0003c0003t0001g0014a0003c0003t0001g0098a0003c0003t0001g0110others(7): Show | 10 | HG02015.hp1 NA18945.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.1235-410G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537970 | ||||||
chr1:183538029
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1235-351A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183538029 | ||||||
chr1:183538204
|
A | G | 1 | a0002c0002t0008g0049 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1235-176A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183538204 | ||||||
chr1:183538270
|
G | A | 6 | a0004c0005t0005g0005a0004c0005t0005g0166a0004c0005t0005g0167others(3): Show | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-110G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183538270 | ||||||
chr1:183538704
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1295+264C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183538704 | ||||||
chr1:183538911
|
G | A | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1295+471G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183538911 | ||||||
chr1:183538926
|
A | G | 1 | a0006c0008t0001g0318 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1295+486A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183538926 | ||||||
chr1:183539184
|
T | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+744T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539184 | ||||||
chr1:183539634
|
G | T | 1 | a0001c0001t0004g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1295+1194G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539634 | ||||||
chr1:183539662
|
A | G | 2 | a0002c0002t0002g0027a0002c0002t0002g0037 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1295+1222A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539662 | ||||||
chr1:183539822
|
A | G | 55 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0124others(52): Show | 60 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1296-1162A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539822 | ||||||
chr1:183539917
|
A | G | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1296-1067A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539917 | ||||||
chr1:183540103
|
A | C | 194 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(191): Show | 208 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1296-881A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183540103 | ||||||
chr1:183540419
|
TA | T | 8 | a0001c0001t0001g0173a0001c0001t0001g0284a0001c0001t0001g0315others(5): Show | 8 | HG01069.hp1 HG01515.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296-552delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr1 | 183540419 | |||||
chr1:183540452
|
G | A | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1296-532G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183540452 | ||||||
chr1:183540719
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1296-265A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183540719 | ||||||
chr1:183541162
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1415+59G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541162 | ||||||
chr1:183541164
|
GCA | G | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1415+65_1415+66del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 183541164 | |||||
chr1:183541410
|
A | G | 2 | a0001c0001t0004g0239a0001c0001t0005g0224 | 2 | NA18960.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1415+307A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541410 | ||||||
chr1:183541523
|
T | A | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415+420T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541523 | ||||||
chr1:183541630
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1416-446C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541630 | ||||||
chr1:183541691
|
A | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416-385A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541691 | ||||||
chr1:183541907
|
C | G | 1 | a0002c0002t0002g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1416-169C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541907 | ||||||
chr1:183541923
|
C | A | 1 | a0001c0001t0019g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1416-153C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541923 | ||||||
chr1:183541990
|
A | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416-86A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541990 | ||||||
chr1:183542021
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1416-55T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183542021 | ||||||
chr1:183542599
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1842+97G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542599 | ||||||
chr1:183542681
|
A | G | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1842+179A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542681 | ||||||
chr1:183542908
|
T | C | 2 | a0001c0001t0004g0243a0001c0001t0007g0217 | 2 | HG00609.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1842+406T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542908 | ||||||
chr1:183542916
|
A | AAT | 3 | a0001c0001t0001g0299a0001c0001t0001g0302a0001c0001t0001g0316 | 3 | HG04184.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1842+425_1842+426d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542916 | |||||
chr1:183542916
|
AAT | A | 13 | a0001c0001t0001g0158a0001c0001t0001g0183a0001c0001t0005g0094others(10): Show | 14 | HG00423.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1842+425_1842+426d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542916 | |||||
chr1:183542925
|
A | ATG | 29 | a0001c0001t0001g0021a0001c0001t0001g0114a0001c0001t0001g0116others(26): Show | 32 | HG00408.hp1 HG01081.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1842+424_1842+425i others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542925
|
A | ATGTG | 20 | a0001c0001t0001g0140a0002c0002t0002g0027a0002c0002t0002g0058others(17): Show | 22 | HG01257.hp1 HG01978.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.1842+424_1842+425i others(6): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542925
|
ATATG | A | 14 | a0001c0001t0001g0325a0001c0001t0005g0095a0001c0001t0005g0096others(11): Show | 17 | HG00140.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1842+425_1842+428d others(6): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542925
|
ATATGTGT others(3): Show |
A | 1 | a0007c0007t0005g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1842+425_1842+434d others(12): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542925
|
ATATGTGT others(7): Show |
A | 13 | a0001c0001t0003g0191a0001c0001t0003g0197a0001c0001t0007g0263others(10): Show | 16 | HG00558.hp2 HG01069.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.1842+425_1842+438d others(16): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542925
|
ATATGTGT others(9): Show |
A | 104 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(101): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1842+425_1842+440d others(18): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542925
|
ATATGTGT others(11): Show |
A | 4 | a0001c0001t0006g0019a0001c0001t0006g0204a0001c0001t0009g0019others(1): Show | 4 | HG02698.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+425_1842+442d others(20): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | |||||
chr1:183542927
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0018g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1842+453_1842+468d others(18): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | |||||
chr1:183542927
|
A | G | 100 | a0001c0001t0001g0021a0001c0001t0001g0082a0001c0001t0001g0114others(97): Show | 109 | HG00408.hp1 HG00597.hp1 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.1842+425A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542927 | ||||||
chr1:183542927
|
ATG | A | 22 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1842+467_1842+468d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | |||||
chr1:183542927
|
ATGTG | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0101a0001c0001t0001g0102others(5): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1842+465_1842+468d others(6): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | |||||
chr1:183542927
|
ATGTGTG | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0173others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+463_1842+468d others(8): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | |||||
chr1:183542931
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1842+429G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542931 | ||||||
chr1:183542933
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1842+431G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542933 | ||||||
chr1:183542950
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0282others(41): Show | 50 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1842+448T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542950 | ||||||
chr1:183543091
|
G | C | 1 | a0001c0001t0001g0301 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1842+589G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543091 | ||||||
chr1:183543470
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1843-883A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543470 | ||||||
chr1:183543487
|
GA | G | 14 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0298others(11): Show | 16 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1843-855delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183543487 | |||||
chr1:183543690
|
C | T | 1 | a0003c0003t0001g0154 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1843-663C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543690 | ||||||
chr1:183543705
|
T | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(315): Show | 345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.1843-648T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543705 | ||||||
chr1:183543706
|
G | A | 1 | a0001c0001t0007g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1843-647G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543706 | ||||||
chr1:183543807
|
G | A | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1843-546G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543807 | ||||||
chr1:183544048
|
C | T | 9 | a0003c0003t0001g0013a0003c0003t0001g0017a0003c0003t0001g0120others(6): Show | 11 | HG00423.hp1 HG01168.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1843-305C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183544048 | ||||||
chr1:183544310
|
A | C | 1 | a0001c0001t0007g0240 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1843-43A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183544310 | ||||||
chr1:183544511
|
G | A | 8 | a0002c0002t0002g0063a0002c0002t0002g0064a0002c0002t0002g0065others(5): Show | 8 | HG01257.hp1 HG01978.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1987+14G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 15/22 | chr1 | 183544511 | ||||||
chr1:183544857
|
A | T | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1988-73A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 15/22 | chr1 | 183544857 | ||||||
chr1:183545396
|
C | A | 16 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0027others(13): Show | 18 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2370+84C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545396 | ||||||
chr1:183545727
|
T | A | 1 | a0001c0001t0004g0218 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2371-239T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545727 | ||||||
chr1:183545896
|
A | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | HG02109.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2371-70A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545896 | ||||||
chr1:183545957
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0013g0269 | 2 | HG03098.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2371-9C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545957 | ||||||
chr1:183546376
|
G | A | 1 | a0002c0002t0002g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2742+39G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546376 | ||||||
chr1:183546386
|
T | C | 1 | a0001c0001t0007g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2742+49T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546386 | ||||||
chr1:183546505
|
A | G | 2 | a0001c0001t0001g0285a0001c0001t0001g0325 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2742+168A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546505 | ||||||
chr1:183546642
|
A | G | 66 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(63): Show | 75 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.2742+305A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546642 | ||||||
chr1:183546965
|
G | C | 193 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(190): Show | 208 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.2743-138G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546965 | ||||||
chr1:183547033
|
A | G | 1 | a0002c0002t0002g0048 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2743-70A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183547033 | ||||||
chr1:183547073
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2743-30G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183547073 | ||||||
chr1:183547296
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2892+44T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547296 | ||||||
chr1:183547305
|
G | A | 102 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(99): Show | 105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.2892+53G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547305 | ||||||
chr1:183547367
|
T | C | 3 | a0001c0001t0003g0215a0001c0001t0006g0212a0001c0001t0006g0219 | 3 | HG01106.hp1 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2892+115T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547367 | ||||||
chr1:183547631
|
T | C | 1 | a0001c0001t0005g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2892+379T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547631 | ||||||
chr1:183547850
|
T | A | 102 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(99): Show | 105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.2892+598T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547850 | ||||||
chr1:183547854
|
A | T | 111 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(108): Show | 115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2892+602A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547854 | ||||||
chr1:183547942
|
G | A | 1 | a0003c0003t0001g0098 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2892+690G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547942 | ||||||
chr1:183548025
|
G | T | 2 | a0007c0007t0005g0171a0007c0007t0005g0172 | 2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2892+773G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548025 | ||||||
chr1:183548146
|
C | T | 1 | a0001c0001t0006g0276 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2892+894C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548146 | ||||||
chr1:183548293
|
G | T | 2 | a0001c0001t0014g0157a0001c0001t0018g0181 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2893-915G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548293 | ||||||
chr1:183548389
|
T | C | 2 | a0002c0002t0002g0059a0002c0002t0002g0060 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2893-819T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548389 | ||||||
chr1:183548398
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(13): Show | 18 | HG01891.hp1 HG02109.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.2893-810C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548398 | ||||||
chr1:183548447
|
T | G | 9 | a0001c0001t0004g0218a0001c0001t0004g0225a0001c0001t0004g0233others(6): Show | 9 | HG00423.hp2 HG00609.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.2893-761T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548447 | ||||||
chr1:183548546
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2893-662A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548546 | ||||||
chr1:183548700
|
T | C | 1 | a0001c0001t0006g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2893-508T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548700 | ||||||
chr1:183548731
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2893-477A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548731 | ||||||
chr1:183548836
|
T | C | 124 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0023others(121): Show | 130 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.2893-372T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548836 | ||||||
chr1:183548837
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2893-371G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548837 | ||||||
chr1:183548871
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2893-337A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548871 | ||||||
chr1:183548902
|
C | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0285others(1): Show | 4 | HG01884.hp1 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2893-306C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548902 | ||||||
chr1:183548979
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2893-229T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548979 | ||||||
chr1:183549106
|
C | T | 1 | a0002c0002t0002g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2893-102C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183549106 | ||||||
chr1:183549107
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2893-101G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183549107 | ||||||
chr1:183549434
|
G | T | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2973+146G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 19/22 | chr1 | 183549434 | ||||||
chr1:183550024
|
G | A | 4 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(1): Show | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3133+101G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550024 | ||||||
chr1:183550060
|
T | C | 1 | a0002c0002t0008g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3133+137T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550060 | ||||||
chr1:183550074
|
GA | G | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3133+162delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 183550074 | |||||
chr1:183550269
|
G | A | 57 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0115others(54): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.3133+346G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550269 | ||||||
chr1:183550286
|
A | T | 2 | a0003c0003t0001g0118a0003c0003t0001g0137 | 2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3133+363A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550286 | ||||||
chr1:183550608
|
T | G | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3134-143T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550608 | ||||||
chr1:183550622
|
T | C | 1 | a0001c0001t0005g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3134-129T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550622 | ||||||
chr1:183551495
|
T | G | 2 | a0001c0001t0014g0157a0001c0001t0018g0181 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3450+305T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 22/22 | chr1 | 183551495 |