geneid | 10232 |
---|---|
ensemblid | ENSG00000102854.16 |
hgncid | 7371 |
symbol | MSLN |
name | mesothelin |
refseq_nuc | NM_005823.6 |
refseq_prot | NP_005814.2 |
ensembl_nuc | ENST00000545450.7 |
ensembl_prot | ENSP00000442965.2 |
mane_status | MANE Select |
chr | chr16 |
start | 760734 |
end | 768862 |
strand | + |
ver | v1.2 |
region | chr16:760734-768862 |
region5000 | chr16:755734-773862 |
regionname0 | MSLN_chr16_760734_768862 |
regionname5000 | MSLN_chr16_755734_773862 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001 | 1/0 | 622 | 160 | 21 | 29 | 86 | 7 | 16 | 62 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002 | 0/1 | 622 | 98 | 22 | 19 | 45 | 2 | 9 | 34 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0003 | 0/0 | 622 | 23 | 14 | 2 | 3 | 1 | 3 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004 | 0/0 | 622 | 17 | 0 | 1 | 9 | 0 | 7 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0005 | 0/0 | 622 | 17 | 2 | 3 | 4 | 0 | 8 | 4 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0006 | 0/0 | 622 | 14 | 11 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0007 | 0/0 | 622 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0008 | 0/0 | 622 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0009 | 0/0 | 284 | 6 | 0 | 3 | 2 | 0 | 1 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0010 | 0/0 | 622 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0011 | 0/0 | 622 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0012 | 0/0 | 622 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0013 | 0/0 | 622 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0014 | 0/0 | 622 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0015 | 0/0 | 622 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0016 | 0/0 | 622 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0017 | 0/0 | 622 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0018 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0019 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0020 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0021 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0022 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0023 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0024 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0025 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0026 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0027 | 0/0 | 165 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0028 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0029 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0030 | 0/0 | 622 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1869 | 148 | 21 | 28 | 77 | 7 | 14 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0002 | 0/1 | 1869 | 66 | 5 | 9 | 43 | 2 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0003 | 0/0 | 1869 | 26 | 12 | 10 | 2 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0004 | 0/0 | 1869 | 23 | 14 | 2 | 3 | 1 | 3 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0005 | 0/0 | 1869 | 16 | 2 | 3 | 4 | 0 | 7 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0006 | 0/0 | 1869 | 12 | 0 | 1 | 5 | 0 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0007 | 0/0 | 1869 | 8 | 6 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0008 | 0/0 | 1869 | 7 | 0 | 0 | 7 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0009 | 0/0 | 1869 | 7 | 7 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0010 | 0/0 | 1869 | 6 | 5 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0011 | 0/0 | 1870 | 5 | 0 | 3 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0012 | 0/0 | 1869 | 5 | 5 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0013 | 0/0 | 1869 | 4 | 3 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0014 | 0/0 | 1869 | 4 | 0 | 3 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0015 | 0/0 | 1869 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0016 | 0/0 | 1869 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0017 | 0/0 | 1869 | 3 | 0 | 0 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0018 | 0/0 | 1869 | 3 | 0 | 3 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0019 | 0/0 | 1869 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0020 | 0/0 | 1869 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0021 | 0/0 | 1869 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0022 | 0/0 | 1869 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0023 | 0/0 | 1869 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0024 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0025 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0026 | 0/0 | 1835 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0027 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0028 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0029 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0030 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0031 | 0/0 | 1870 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0032 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0033 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0034 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0035 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0036 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0037 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0038 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0039 | 0/0 | 1868 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0040 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0041 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0042 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0043 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0044 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0045 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0046 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0047 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
c0048 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 329 | 244 | 44 | 51 | 105 | 9 | 34 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0002 | 0/1 | 329 | 85 | 18 | 10 | 45 | 2 | 9 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0003 | 0/0 | 329 | 30 | 20 | 2 | 4 | 1 | 3 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0004 | 0/0 | 329 | 15 | 8 | 7 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0005 | 0/0 | 329 | 4 | 3 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0006 | 0/0 | 328 | 2 | 1 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0007 | 0/0 | 328 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0008 | 0/0 | 304 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0009 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0010 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0011 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0012 | 0/0 | 329 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
t0013 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0002 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0316 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0039 | 0/0 | 1868 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0001 | 1/0 | 1869 | 148 | 21 | 28 | 77 | 7 | 14 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0008 | 0/0 | 1869 | 7 | 0 | 0 | 7 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0022 | 0/0 | 1869 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0035 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0038 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0041 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0002 | 0/1 | 1869 | 66 | 5 | 9 | 43 | 2 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0003 | 0/0 | 1869 | 26 | 12 | 10 | 2 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0015 | 0/0 | 1869 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0025 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0034 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0003c0004 | 0/0 | 1869 | 23 | 14 | 2 | 3 | 1 | 3 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004c0006 | 0/0 | 1869 | 12 | 0 | 1 | 5 | 0 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004c0017 | 0/0 | 1869 | 3 | 0 | 0 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004c0021 | 0/0 | 1869 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0005c0005 | 0/0 | 1869 | 16 | 2 | 3 | 4 | 0 | 7 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0005c0045 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0006c0007 | 0/0 | 1869 | 8 | 6 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0006c0010 | 0/0 | 1869 | 6 | 5 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0007c0012 | 0/0 | 1869 | 5 | 5 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0007c0016 | 0/0 | 1869 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0008c0009 | 0/0 | 1869 | 7 | 7 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0009c0011 | 0/0 | 1870 | 5 | 0 | 3 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0009c0031 | 0/0 | 1870 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0010c0013 | 0/0 | 1869 | 4 | 3 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0011c0014 | 0/0 | 1869 | 4 | 0 | 3 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0012c0018 | 0/0 | 1869 | 3 | 0 | 3 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0013c0019 | 0/0 | 1869 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0014c0024 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0014c0047 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0015c0020 | 0/0 | 1869 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0016c0028 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0016c0029 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0017c0023 | 0/0 | 1869 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0018c0027 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0019c0032 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0020c0033 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0021c0043 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0022c0036 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0023c0037 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0024c0040 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0025c0042 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0026c0030 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0027c0026 | 0/0 | 1835 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0028c0044 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0029c0046 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0030c0048 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0039t0008 | 0/0 | 2171 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0001t0001 | 1/0 | 2197 | 145 | 21 | 27 | 75 | 7 | 14 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0001t0005 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0001t0010 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0001t0011 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0008t0001 | 0/0 | 2197 | 7 | 0 | 0 | 7 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0022t0001 | 0/0 | 2197 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0035t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0038t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0001c0041t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0002t0002 | 0/1 | 2197 | 65 | 5 | 8 | 43 | 2 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0002t0012 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0003t0001 | 0/0 | 2197 | 4 | 0 | 1 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0003t0002 | 0/0 | 2197 | 7 | 4 | 2 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0003t0004 | 0/0 | 2197 | 15 | 8 | 7 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0015t0003 | 0/0 | 2197 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0025t0002 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0002c0034t0003 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0003c0004t0003 | 0/0 | 2197 | 23 | 14 | 2 | 3 | 1 | 3 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004c0006t0001 | 0/0 | 2197 | 12 | 0 | 1 | 5 | 0 | 6 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004c0017t0001 | 0/0 | 2197 | 3 | 0 | 0 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0004c0021t0001 | 0/0 | 2197 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0005c0005t0001 | 0/0 | 2197 | 15 | 1 | 3 | 4 | 0 | 7 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0005c0005t0009 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0005c0045t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0006c0007t0001 | 0/0 | 2197 | 8 | 6 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0006c0010t0001 | 0/0 | 2197 | 6 | 5 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0007c0012t0001 | 0/0 | 2197 | 5 | 5 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0007c0016t0001 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0007c0016t0005 | 0/0 | 2197 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0008c0009t0002 | 0/0 | 2197 | 7 | 7 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0009c0011t0001 | 0/0 | 2198 | 5 | 0 | 3 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0009c0031t0002 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0010c0013t0006 | 0/0 | 2196 | 2 | 1 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0010c0013t0007 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0011c0014t0001 | 0/0 | 2197 | 4 | 0 | 3 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0012c0018t0001 | 0/0 | 2197 | 3 | 0 | 3 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0013c0019t0001 | 0/0 | 2197 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0014c0024t0002 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0014c0024t0013 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0014c0047t0003 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0015c0020t0002 | 0/0 | 2197 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0016c0028t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0016c0029t0001 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0017c0023t0001 | 0/0 | 2197 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0018c0027t0003 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0019c0032t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0020c0033t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0021c0043t0001 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0022c0036t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0023c0037t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0024c0040t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0025c0042t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0026c0030t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0027c0026t0001 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0028c0044t0002 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0029c0046t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
a0030c0048t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | copy fasta | chr16 | 755734 | 773862 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0039t0008g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0011g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0008t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0022t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0022t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0035t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0038t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0041t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0316 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0012g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0025t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0034t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0002 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0017t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0017t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0017t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0021t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0021t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0045t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0007t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0010t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0010t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0010t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0010t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0010t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0012t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0012t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0012t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0016t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0016t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0016t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0009t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0011t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0011t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0011t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0011t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0011t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0031t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0010c0013t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0010c0013t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0010c0013t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0010c0013t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0011c0014t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0011c0014t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0012c0018t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0012c0018t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0012c0018t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0013c0019t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0014c0024t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0014c0024t0013g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0014c0047t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0015c0020t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0015c0020t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0016c0028t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0016c0029t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0017c0023t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0017c0023t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0018c0027t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0019c0032t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0020c0033t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0021c0043t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0022c0036t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0023c0037t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0024c0040t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0025c0042t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0026c0030t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0027c0026t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0028c0044t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0029c0046t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0030c0048t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0314 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0354 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00140 | hp2 | a0030 | c0048 | t0001 | g0155 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00423 | hp2 | a0003 | c0004 | t0003 | g0269 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00558 | hp1 | a0004 | c0021 | t0001 | g0298 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00609 | hp2 | a0029 | c0046 | t0001 | g0034 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0344 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0343 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00639 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00639 | hp2 | a0005 | c0005 | t0001 | g0036 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00642 | hp1 | a0004 | c0006 | t0001 | g0267 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0074 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0159 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00738 | hp2 | a0005 | c0005 | t0001 | g0031 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00741 | hp1 | a0011 | c0014 | t0001 | g0003 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01069 | hp2 | a0006 | c0007 | t0001 | g0014 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01071 | hp1 | a0006 | c0007 | t0001 | g0014 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01074 | hp1 | a0005 | c0005 | t0001 | g0198 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0320 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01081 | hp2 | a0011 | c0014 | t0001 | g0003 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01099 | hp1 | a0017 | c0023 | t0001 | g0020 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01099 | hp2 | a0024 | c0040 | t0001 | g0287 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01106 | hp2 | a0003 | c0004 | t0003 | g0016 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0334 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01109 | hp2 | a0009 | c0011 | t0001 | g0005 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01169 | hp2 | a0011 | c0014 | t0001 | g0145 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01175 | hp1 | a0027 | c0026 | t0001 | g0169 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01175 | hp2 | a0009 | c0011 | t0001 | g0184 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0327 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01192 | hp2 | a0000 | c0039 | t0008 | g0146 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01243 | hp2 | a0010 | c0013 | t0006 | g0209 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0326 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01256 | hp2 | a0012 | c0018 | t0001 | g0078 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0322 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01361 | hp1 | a0001 | c0022 | t0001 | g0270 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01496 | hp1 | a0023 | c0037 | t0001 | g0123 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01496 | hp2 | a0025 | c0042 | t0001 | g0170 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0317 | EUR | IBS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01884 | hp1 | a0016 | c0029 | t0001 | g0225 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01884 | hp2 | a0003 | c0004 | t0003 | g0019 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01891 | hp1 | a0003 | c0004 | t0003 | g0002 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01891 | hp2 | a0008 | c0009 | t0002 | g0045 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01934 | hp2 | a0002 | c0003 | t0002 | g0260 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01943 | hp1 | a0026 | c0030 | t0001 | g0129 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01943 | hp2 | a0002 | c0003 | t0004 | g0213 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01952 | hp2 | a0002 | c0003 | t0004 | g0216 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01978 | hp1 | a0002 | c0003 | t0004 | g0212 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0333 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01981 | hp1 | a0006 | c0010 | t0001 | g0239 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01993 | hp2 | a0012 | c0018 | t0001 | g0079 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02004 | hp1 | a0002 | c0003 | t0004 | g0220 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02004 | hp2 | a0002 | c0002 | t0012 | g0315 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02015 | hp1 | a0009 | c0011 | t0001 | g0101 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0329 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0140 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02040 | hp1 | a0001 | c0008 | t0001 | g0303 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02055 | hp1 | a0007 | c0012 | t0001 | g0004 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02055 | hp2 | a0008 | c0009 | t0002 | g0047 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02056 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02071 | hp2 | a0004 | c0006 | t0001 | g0261 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02080 | hp2 | a0004 | c0006 | t0001 | g0265 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02083 | hp1 | a0003 | c0004 | t0003 | g0278 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02129 | hp1 | a0001 | c0038 | t0001 | g0083 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0335 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02155 | hp2 | a0015 | c0020 | t0002 | g0297 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02257 | hp2 | a0010 | c0013 | t0007 | g0207 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0274 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02258 | hp2 | a0006 | c0010 | t0001 | g0238 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02273 | hp1 | a0002 | c0003 | t0004 | g0217 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02280 | hp2 | a0007 | c0016 | t0001 | g0043 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02293 | hp2 | a0002 | c0003 | t0004 | g0215 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02300 | hp2 | a0002 | c0003 | t0004 | g0214 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02451 | hp1 | a0013 | c0019 | t0001 | g0006 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02451 | hp2 | a0006 | c0007 | t0001 | g0023 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02523 | hp2 | a0015 | c0020 | t0002 | g0296 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02572 | hp1 | a0010 | c0013 | t0007 | g0208 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02572 | hp2 | a0013 | c0019 | t0001 | g0006 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02602 | hp1 | a0004 | c0006 | t0001 | g0346 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02615 | hp1 | a0006 | c0007 | t0001 | g0258 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02615 | hp2 | a0006 | c0010 | t0001 | g0236 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02622 | hp2 | a0014 | c0024 | t0002 | g0029 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02630 | hp1 | a0008 | c0009 | t0002 | g0044 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02630 | hp2 | a0008 | c0009 | t0002 | g0028 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0249 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02647 | hp2 | a0002 | c0003 | t0004 | g0230 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02717 | hp2 | a0007 | c0016 | t0005 | g0229 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02723 | hp1 | a0003 | c0004 | t0003 | g0002 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02735 | hp1 | a0003 | c0004 | t0003 | g0275 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0194 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02809 | hp1 | a0007 | c0012 | t0001 | g0004 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02818 | hp1 | a0002 | c0003 | t0004 | g0233 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02818 | hp2 | a0003 | c0004 | t0003 | g0227 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02886 | hp1 | a0002 | c0003 | t0002 | g0248 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02895 | hp1 | a0003 | c0004 | t0003 | g0352 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02965 | hp1 | a0008 | c0009 | t0002 | g0046 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02965 | hp2 | a0002 | c0003 | t0004 | g0232 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02970 | hp1 | a0007 | c0016 | t0005 | g0012 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02970 | hp2 | a0006 | c0010 | t0001 | g0013 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02976 | hp1 | a0002 | c0003 | t0004 | g0218 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02976 | hp2 | a0003 | c0004 | t0003 | g0019 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03017 | hp2 | a0001 | c0035 | t0001 | g0206 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03041 | hp2 | a0007 | c0016 | t0005 | g0012 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0328 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03098 | hp2 | a0007 | c0012 | t0001 | g0245 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03130 | hp2 | a0002 | c0003 | t0004 | g0234 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03139 | hp1 | a0006 | c0007 | t0001 | g0228 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03139 | hp2 | a0010 | c0013 | t0006 | g0210 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03195 | hp2 | a0005 | c0005 | t0001 | g0038 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03209 | hp1 | a0003 | c0004 | t0003 | g0002 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03209 | hp2 | a0008 | c0009 | t0002 | g0257 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03225 | hp2 | a0002 | c0003 | t0002 | g0253 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03239 | hp1 | a0005 | c0005 | t0001 | g0035 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0102 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03453 | hp1 | a0003 | c0004 | t0003 | g0002 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03486 | hp1 | a0005 | c0005 | t0009 | g0032 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03486 | hp2 | a0002 | c0034 | t0003 | g0259 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03490 | hp2 | a0005 | c0005 | t0001 | g0009 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03492 | hp2 | a0005 | c0005 | t0001 | g0009 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03516 | hp1 | a0002 | c0003 | t0004 | g0219 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03540 | hp1 | a0007 | c0012 | t0001 | g0004 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03540 | hp2 | a0007 | c0012 | t0001 | g0246 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03579 | hp1 | a0002 | c0015 | t0003 | g0256 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03579 | hp2 | a0006 | c0007 | t0001 | g0254 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0268 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03654 | hp2 | a0005 | c0005 | t0001 | g0041 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03669 | hp1 | a0001 | c0022 | t0001 | g0178 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03669 | hp2 | a0005 | c0005 | t0001 | g0022 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03688 | hp1 | a0003 | c0004 | t0003 | g0276 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03688 | hp2 | a0005 | c0005 | t0001 | g0027 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0330 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03704 | hp2 | a0002 | c0025 | t0002 | g0293 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03710 | hp1 | a0003 | c0004 | t0003 | g0271 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03710 | hp2 | a0022 | c0036 | t0001 | g0183 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03834 | hp1 | a0004 | c0017 | t0001 | g0263 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03927 | hp1 | a0004 | c0006 | t0001 | g0224 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0312 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04115 | hp1 | a0004 | c0006 | t0001 | g0181 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04184 | hp1 | a0009 | c0031 | t0002 | g0353 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04184 | hp2 | a0005 | c0045 | t0001 | g0040 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0289 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0332 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04204 | hp1 | a0004 | c0006 | t0001 | g0251 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04204 | hp2 | a0004 | c0006 | t0001 | g0240 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04228 | hp1 | a0004 | c0006 | t0001 | g0350 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18522 | hp1 | a0002 | c0003 | t0002 | g0247 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18522 | hp2 | a0002 | c0003 | t0004 | g0231 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0310 | EAS | CHB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18906 | hp1 | a0021 | c0043 | t0001 | g0008 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18906 | hp2 | a0002 | c0015 | t0003 | g0066 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18939 | hp1 | a0001 | c0008 | t0001 | g0306 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0337 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18946 | hp2 | a0001 | c0008 | t0001 | g0305 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18949 | hp2 | a0004 | c0017 | t0001 | g0264 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18950 | hp1 | a0020 | c0033 | t0001 | g0342 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18950 | hp2 | a0001 | c0008 | t0001 | g0300 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18959 | hp1 | a0005 | c0005 | t0001 | g0037 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0202 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18969 | hp1 | a0004 | c0017 | t0001 | g0142 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18969 | hp2 | a0004 | c0006 | t0001 | g0266 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18980 | hp1 | a0005 | c0005 | t0001 | g0039 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18995 | hp2 | a0005 | c0005 | t0001 | g0033 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18999 | hp1 | a0001 | c0008 | t0001 | g0304 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19007 | hp1 | a0001 | c0008 | t0001 | g0301 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19012 | hp1 | a0014 | c0047 | t0003 | g0030 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19030 | hp1 | a0018 | c0027 | t0003 | g0015 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19030 | hp2 | a0028 | c0044 | t0002 | g0250 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19043 | hp2 | a0006 | c0007 | t0001 | g0008 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19055 | hp1 | a0004 | c0021 | t0001 | g0345 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19057 | hp1 | a0004 | c0006 | t0001 | g0185 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19063 | hp2 | a0019 | c0032 | t0001 | g0177 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19066 | hp2 | a0001 | c0041 | t0001 | g0152 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19079 | hp1 | a0001 | c0008 | t0001 | g0302 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19083 | hp1 | a0004 | c0006 | t0001 | g0262 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19083 | hp2 | a0009 | c0011 | t0001 | g0340 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19084 | hp2 | a0003 | c0004 | t0003 | g0277 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19088 | hp2 | a0016 | c0028 | t0001 | g0187 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19089 | hp1 | a0005 | c0005 | t0001 | g0025 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19240 | hp1 | a0006 | c0010 | t0001 | g0013 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0295 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20129 | hp1 | a0003 | c0004 | t0003 | g0273 | AFR | ASW | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20129 | hp2 | a0002 | c0015 | t0003 | g0174 | AFR | ASW | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20752 | hp2 | a0011 | c0014 | t0001 | g0003 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20805 | hp2 | a0003 | c0004 | t0003 | g0016 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20905 | hp1 | a0005 | c0005 | t0001 | g0024 | SAS | GIH | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20905 | hp2 | a0017 | c0023 | t0001 | g0021 | SAS | GIH | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01123 | hp1 | a0012 | c0018 | t0001 | g0186 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01123 | hp2 | a0009 | c0011 | t0001 | g0203 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02109 | hp1 | a0002 | c0015 | t0003 | g0255 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02109 | hp2 | a0003 | c0004 | t0003 | g0015 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02486 | hp1 | a0006 | c0010 | t0001 | g0237 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02486 | hp2 | a0003 | c0004 | t0003 | g0291 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02559 | hp1 | a0008 | c0009 | t0002 | g0048 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02559 | hp2 | a0003 | c0004 | t0003 | g0272 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03471 | hp1 | a0013 | c0019 | t0001 | g0006 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG06807 | hp1 | a0006 | c0007 | t0001 | g0026 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20300 | hp2 | a0014 | c0024 | t0013 | g0290 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA21309 | hp1 | a0002 | c0003 | t0004 | g0211 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA21309 | hp2 | a0003 | c0004 | t0003 | g0226 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0316 | REF | REF | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0053 | REF | REF | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:763260
|
C | T | 1 | a0030 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.113C>T | p.Ala38Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/18 | 312/2197 | 113/1869 | 38/622 | chr16 | 763260 | ||
chr16:764058
|
C | T | 5 | a0005a0008a0014others(2): Show | 29 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(26): Show |
missense_variant | MODERATE | c.215C>T | p.Ala72Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/18 | 414/2197 | 215/1869 | 72/622 | chr16 | 764058 | ||
chr16:764091
|
G | A | 1 | a0015 | 2 | HG02155.hp2 HG02523.hp2 |
missense_variant | MODERATE | c.248G>A | p.Arg83Gln | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/18 | 447/2197 | 248/1869 | 83/622 | chr16 | 764091 | ||
chr16:764648
|
TGCGCTGT others(27): Show |
T | 1 | a0027 | 1 | HG01175.hp1 | frameshift_variant | HIGH | c.304_337delCGCTGTCT others(26): Show |
p.Cys103fs | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/18 | 503/2197 | 304/1869 | 102/622 | INFO_REALIGN_3_PRIME | chr16 | 764648 | |
chr16:764698
|
C | G | 1 | a0013 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.352C>G | p.Leu118Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/18 | 551/2197 | 352/1869 | 118/622 | chr16 | 764698 | ||
chr16:764942
|
G | A | 4 | a0003a0013a0016others(1): Show | 29 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(26): Show |
missense_variant | MODERATE | c.416G>A | p.Arg139His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 8/18 | 615/2197 | 416/1869 | 139/622 | chr16 | 764942 | ||
chr16:765110
|
G | A | 1 | a0026 | 1 | HG01943.hp1 | missense_variant&splice_region_variant | MODERATE | c.511G>A | p.Gly171Ser | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/18 | 710/2197 | 511/1869 | 171/622 | chr16 | 765110 | ||
chr16:765214
|
A | AC | 3 | a0009a0018a0028 | 8 | HG01109.hp2 HG01123.hp2 HG01175.hp2 others(5): Show |
frameshift_variant | HIGH | c.619dupC | p.Arg207fs | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/18 | 819/2197 | 620/1869 | 207/622 | INFO_REALIGN_3_PRIME | chr16 | 765214 | |
chr16:765549
|
T | C | 3 | a0004a0019a0020 | 19 | HG00558.hp1 HG00642.hp1 HG02071.hp2 others(16): Show |
missense_variant | MODERATE | c.727T>C | p.Ser243Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/18 | 926/2197 | 727/1869 | 243/622 | chr16 | 765549 | ||
chr16:765565
|
T | C | 3 | a0004a0019a0020 | 19 | HG00558.hp1 HG00642.hp1 HG02071.hp2 others(16): Show |
missense_variant | MODERATE | c.743T>C | p.Leu248Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/18 | 942/2197 | 743/1869 | 248/622 | chr16 | 765565 | ||
chr16:765593
|
G | C | 2 | a0008a0028 | 8 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.771G>C | p.Gln257His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/18 | 970/2197 | 771/1869 | 257/622 | chr16 | 765593 | ||
chr16:765692
|
G | A | 1 | a0019 | 1 | NA19063.hp2 | missense_variant&splice_region_variant | MODERATE | c.797G>A | p.Gly266Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/18 | 996/2197 | 797/1869 | 266/622 | chr16 | 765692 | ||
chr16:766089
|
G | A | 1 | a0010 | 4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.926G>A | p.Arg309His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1125/2197 | 926/1869 | 309/622 | chr16 | 766089 | ||
chr16:766091
|
G | A | 2 | a0019a0020 | 2 | NA18950.hp1 NA19063.hp2 |
missense_variant | MODERATE | c.928G>A | p.Glu310Lys | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1127/2197 | 928/1869 | 310/622 | chr16 | 766091 | ||
chr16:766149
|
C | T | 1 | a0012 | 3 | HG01123.hp1 HG01256.hp2 HG01993.hp2 |
missense_variant | MODERATE | c.986C>T | p.Ala329Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1185/2197 | 986/1869 | 329/622 | chr16 | 766149 | ||
chr16:766464
|
A | G | 2 | a0006a0021 | 15 | HG01069.hp2 HG01071.hp1 HG01981.hp1 others(12): Show |
missense_variant | MODERATE | c.1204A>G | p.Asn402Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/18 | 1403/2197 | 1204/1869 | 402/622 | chr16 | 766464 | ||
chr16:766973
|
A | G | 2 | a0007a0013 | 12 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
missense_variant | MODERATE | c.1462A>G | p.Asn488Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/18 | 1661/2197 | 1462/1869 | 488/622 | chr16 | 766973 | ||
chr16:766977
|
G | A | 3 | a0011a0027a0030 | 6 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
missense_variant | MODERATE | c.1466G>A | p.Gly489Glu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/18 | 1665/2197 | 1466/1869 | 489/622 | chr16 | 766977 | ||
chr16:768446
|
G | A | 1 | a0022 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1664G>A | p.Arg555Gln | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1863/2197 | 1664/1869 | 555/622 | chr16 | 768446 | ||
chr16:768452
|
G | A | 1 | a0017 | 2 | HG01099.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1670G>A | p.Arg557His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1869/2197 | 1670/1869 | 557/622 | chr16 | 768452 | ||
chr16:768482
|
G | A | 1 | a0023 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1700G>A | p.Arg567Gln | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1899/2197 | 1700/1869 | 567/622 | chr16 | 768482 | ||
chr16:768533
|
A | G | 1 | a0025 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1751A>G | p.Asn584Ser | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1950/2197 | 1751/1869 | 584/622 | chr16 | 768533 | ||
chr16:768559
|
A | G | 11 | a0002a0003a0007others(8): Show | 152 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(149): Show |
missense_variant | MODERATE | c.1777A>G | p.Met593Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1976/2197 | 1777/1869 | 593/622 | chr16 | 768559 | ||
chr16:768687
|
C | T | 1 | a0024 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1823C>T | p.Pro608Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2022/2197 | 1823/1869 | 608/622 | chr16 | 768687 | ||
chr16:768728
|
G | C | 1 | a0029 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1864G>C | p.Ala622Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2063/2197 | 1864/1869 | 622/622 | chr16 | 768728 | ||
chr16:768731
|
T | A | 1 | a0000 | 1 | HG01192.hp2 | stop_lost | HIGH | c.1867T>A | p.Ter623Argext*? | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2066/2197 | 1867/1869 | 623/622 | chr16 | 768731 | ||
chr16:768732
|
GAGGGCCC others(19): Show |
G | 1 | a0000 | 1 | HG01192.hp2 | frameshift_variant&stop_lost | HIGH | c.1869_*25delAGGGCCC others(19): Show |
p.Ter623fs | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2068/2197 | 1869/1869 | 623/622 | chr16 | 768732 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:763650
|
G | A | 5 | a0001c0008a0002c0002a0002c0025others(2): Show | 78 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(75): Show |
synonymous_variant | LOW | c.138G>A | p.Ala46Ala | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/18 | 337/2197 | 138/1869 | 46/622 | chr16 | 763650 | ||
chr16:764649
|
G | T | 1 | a0007c0016 | 4 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.303G>T | p.Leu101Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/18 | 502/2197 | 303/1869 | 101/622 | chr16 | 764649 | ||
chr16:765202
|
C | T | 1 | a0006c0010 | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.603C>T | p.Ala201Ala | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/18 | 802/2197 | 603/1869 | 201/622 | chr16 | 765202 | ||
chr16:766072
|
T | C | 9 | a0001c0022a0002c0034a0004c0006others(6): Show | 24 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(21): Show |
synonymous_variant | LOW | c.909T>C | p.Pro303Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1108/2197 | 909/1869 | 303/622 | chr16 | 766072 | ||
chr16:766099
|
C | T | 1 | a0002c0034 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.936C>T | p.Asp312Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1135/2197 | 936/1869 | 312/622 | chr16 | 766099 | ||
chr16:766406
|
G | A | 1 | a0001c0035 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1146G>A | p.Glu382Glu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/18 | 1345/2197 | 1146/1869 | 382/622 | chr16 | 766406 | ||
chr16:767407
|
C | T | 6 | a0002c0015a0002c0034a0003c0004others(3): Show | 34 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(31): Show |
synonymous_variant | LOW | c.1533C>T | p.Leu511Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/18 | 1732/2197 | 1533/1869 | 511/622 | chr16 | 767407 | ||
chr16:767458
|
G | A | 1 | a0002c0025 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1584G>A | p.Thr528Thr | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/18 | 1783/2197 | 1584/1869 | 528/622 | chr16 | 767458 | ||
chr16:768555
|
C | T | 8 | a0001c0022a0001c0041a0004c0006others(5): Show | 21 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(18): Show |
synonymous_variant | LOW | c.1773C>T | p.Leu591Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1972/2197 | 1773/1869 | 591/622 | chr16 | 768555 | ||
chr16:768658
|
G | A | 1 | a0001c0038 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1794G>A | p.Ser598Ser | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 1993/2197 | 1794/1869 | 598/622 | chr16 | 768658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:760757
|
C | T | 3 | a0001c0001t0005a0002c0003t0004a0007c0016t0005 | 19 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-176C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/18 | chr16 | 760757 | ||||||
chr16:760758
|
G | A | 1 | a0010c0013t0006 | 2 | HG01243.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-175G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/18 | 1923 | chr16 | 760758 | |||||
chr16:760783
|
C | T | 1 | a0014c0024t0013 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/18 | 1898 | chr16 | 760783 | |||||
chr16:761110
|
C | T | 1 | a0002c0002t0012 | 1 | HG02004.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-74C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/18 | chr16 | 761110 | ||||||
chr16:761113
|
C | CTGCTGTG others(3): Show |
1 | a0001c0001t0011 | 1 | NA18959.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70_-61dupTGCTGTGA others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/18 | 1557 | INFO_REALIGN_3_PRIME | chr16 | 761113 | ||||
chr16:761166
|
C | G | 1 | a0001c0001t0010 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/18 | 1515 | chr16 | 761166 | |||||
chr16:768759
|
G | C | 1 | a0000c0039t0008 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 26 | chr16 | 768759 | |||||
chr16:768797
|
G | A | 1 | a0005c0005t0009 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 64 | chr16 | 768797 | |||||
chr16:768802
|
G | A | 11 | a0002c0002t0002a0002c0002t0012a0002c0003t0002others(8): Show | 102 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 69 | chr16 | 768802 | |||||
chr16:768807
|
C | T | 7 | a0002c0015t0003a0002c0034t0003a0003c0004t0003others(4): Show | 34 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*74C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 74 | chr16 | 768807 | |||||
chr16:768849
|
GC | G | 2 | a0010c0013t0006a0010c0013t0007 | 4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*121delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 121 | INFO_REALIGN_3_PRIME | chr16 | 768849 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:760844
|
T | A | 2 | a0017c0023t0001g0020a0017c0023t0001g0021 | 2 | HG01099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-112+23T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760844 | ||||||
chr16:760921
|
C | T | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0009c0031t0002g0353 | 3 | HG00140.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-112+100C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760921 | ||||||
chr16:760934
|
G | A | 30 | a0001c0001t0001g0042a0005c0005t0001g0009a0005c0005t0001g0022others(27): Show | 31 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-112+113G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760934 | ||||||
chr16:760947
|
C | T | 2 | a0003c0004t0003g0019a0003c0004t0003g0352 | 3 | HG01884.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-112+126C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760947 | ||||||
chr16:760972
|
G | C | 2 | a0017c0023t0001g0020a0017c0023t0001g0021 | 2 | HG01099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-111-101G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760972 | ||||||
chr16:760975
|
G | C | 1 | a0002c0002t0002g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-111-98G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760975 | ||||||
chr16:761029
|
C | T | 1 | a0001c0001t0001g0351 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-111-44C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 761029 | ||||||
chr16:761199
|
C | T | 354 | a0000c0039t0008g0146a0001c0001t0001g0005a0001c0001t0001g0010others(351): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.-10+25C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761199 | ||||||
chr16:761325
|
C | T | 1 | a0004c0006t0001g0350 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-10+151C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761325 | ||||||
chr16:761338
|
G | A | 1 | a0002c0002t0002g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-10+164G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761338 | ||||||
chr16:761347
|
C | T | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-10+173C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761347 | ||||||
chr16:761348
|
G | A | 1 | a0005c0005t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-10+174G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761348 | ||||||
chr16:761382
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-10+208C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761382 | ||||||
chr16:761410
|
G | A | 1 | a0002c0002t0002g0055 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-10+236G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761410 | ||||||
chr16:761433
|
A | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0205others(194): Show | 223 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.-10+259A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761433 | ||||||
chr16:761629
|
TG | T | 162 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0204others(159): Show | 186 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.-10+463delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 761629 | |||||
chr16:761746
|
C | T | 62 | a0001c0001t0001g0292a0001c0001t0001g0339a0001c0001t0001g0341others(59): Show | 73 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10+572C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761746 | ||||||
chr16:761803
|
G | A | 1 | a0005c0005t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-10+629G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761803 | ||||||
chr16:761904
|
C | G | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-10+730C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761904 | ||||||
chr16:761938
|
C | G | 5 | a0008c0009t0002g0044a0008c0009t0002g0045a0008c0009t0002g0046others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-734C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761938 | ||||||
chr16:761946
|
C | G | 45 | a0001c0001t0001g0042a0001c0001t0001g0199a0001c0001t0001g0200others(42): Show | 47 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9-726C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761946 | ||||||
chr16:762008
|
C | A | 36 | a0001c0001t0001g0042a0002c0002t0002g0289a0005c0005t0001g0009others(33): Show | 38 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9-664C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762008 | ||||||
chr16:762030
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9-642G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762030 | ||||||
chr16:762273
|
A | G | 206 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0195others(203): Show | 232 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-9-399A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762273 | ||||||
chr16:762274
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9-398A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762274 | ||||||
chr16:762306
|
T | C | 1 | a0002c0025t0002g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-9-366T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762306 | ||||||
chr16:762539
|
C | T | 31 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(28): Show | 39 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.-9-133C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762539 | ||||||
chr16:762638
|
A | AG | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0002c0002t0002g0188others(3): Show | 6 | HG02080.hp1 HG02155.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-29dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 762638 | |||||
chr16:762848
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.85+83C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 762848 | ||||||
chr16:762889
|
G | C | 1 | a0006c0010t0001g0236 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.85+124G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 762889 | ||||||
chr16:763120
|
T | C | 4 | a0010c0013t0006g0209a0010c0013t0006g0210a0010c0013t0007g0207others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-113T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 763120 | ||||||
chr16:763165
|
C | T | 1 | a0012c0018t0001g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.86-68C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 763165 | ||||||
chr16:763307
|
G | T | 2 | a0010c0013t0006g0209a0010c0013t0006g0210 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.129+31G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763307 | ||||||
chr16:763327
|
G | A | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+51G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763327 | ||||||
chr16:763339
|
T | C | 1 | a0002c0002t0002g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+63T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763339 | ||||||
chr16:763388
|
G | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG00423.hp1 HG02056.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+112G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763388 | ||||||
chr16:763602
|
A | T | 1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.130-40A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763602 | ||||||
chr16:763742
|
G | T | 1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.179+51G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763742 | ||||||
chr16:763764
|
C | CCCATCCC others(128): Show |
1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179+75_179+76insAT others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763764 | |||||
chr16:763768
|
A | ATCCCCCA others(126): Show |
4 | a0008c0009t0002g0044a0008c0009t0002g0045a0008c0009t0002g0046others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763768 | |||||
chr16:763768
|
A | C | 1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179+77A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763768 | ||||||
chr16:763775
|
A | AGCATCCC others(142): Show |
1 | a0002c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(147): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(127): Show |
1 | a0001c0001t0001g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
1 | a0004c0006t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(115): Show |
4 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(127): Show |
1 | a0002c0002t0002g0235 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
58 | a0001c0001t0001g0065a0001c0008t0001g0300a0001c0008t0001g0301others(55): Show | 69 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
51 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 62 | HG00639.hp1 HG01099.hp1 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
1 | a0001c0001t0001g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(127): Show |
1 | a0001c0001t0001g0072 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(124): Show |
1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(129): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(127): Show |
1 | a0001c0001t0011g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
1 | a0002c0002t0002g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
184 | a0000c0039t0008g0146a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(141): Show |
17 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0005g0221others(14): Show | 17 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(146): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(125): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
15 | a0001c0022t0001g0270a0002c0003t0002g0260a0002c0003t0002g0268others(12): Show | 15 | HG00423.hp2 HG00642.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(128): Show |
1 | a0010c0013t0007g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(127): Show |
1 | a0001c0001t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(162): Show |
1 | a0001c0001t0001g0349 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(167): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(83): Show |
1 | a0001c0001t0001g0347 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
2 | a0002c0002t0002g0196a0002c0002t0002g0197 | 2 | NA19003.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(126): Show |
1 | a0022c0036t0001g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(128): Show |
1 | a0009c0011t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | AGCATCCC others(125): Show |
3 | a0007c0016t0001g0043a0007c0016t0005g0012a0007c0016t0005g0229 | 4 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | |||||
chr16:763775
|
A | C | 1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179+84A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763775 | ||||||
chr16:763776
|
G | GCATCCCA others(126): Show |
1 | a0012c0018t0001g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763776 | |||||
chr16:763780
|
C | CCCATCCC others(125): Show |
1 | a0002c0002t0002g0338 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763780 | |||||
chr16:763783
|
C | A | 4 | a0008c0009t0002g0044a0008c0009t0002g0045a0008c0009t0002g0046others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+92C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763783 | ||||||
chr16:763891
|
G | A | 3 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-132G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763891 | ||||||
chr16:763900
|
G | C | 16 | a0001c0001t0005g0221a0002c0003t0004g0211a0002c0003t0004g0212others(13): Show | 16 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.180-123G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763900 | ||||||
chr16:763917
|
C | T | 1 | a0024c0040t0001g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.180-106C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763917 | ||||||
chr16:763955
|
T | C | 17 | a0001c0022t0001g0270a0002c0003t0002g0260a0002c0003t0002g0268others(14): Show | 17 | HG00423.hp2 HG00642.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.180-68T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763955 | ||||||
chr16:763975
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-48T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763975 | ||||||
chr16:763977
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-46G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763977 | ||||||
chr16:763978
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-45C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763978 | ||||||
chr16:763980
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-43G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763980 | ||||||
chr16:763981
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-42G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763981 | ||||||
chr16:763983
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-40G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763983 | ||||||
chr16:763984
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-39A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763984 | ||||||
chr16:763985
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-38G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763985 | ||||||
chr16:763987
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-36G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763987 | ||||||
chr16:763988
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-35G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763988 | ||||||
chr16:764243
|
C | T | 17 | a0001c0022t0001g0270a0002c0003t0002g0260a0002c0003t0002g0268others(14): Show | 17 | HG00423.hp2 HG00642.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.300+100C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764243 | ||||||
chr16:764275
|
C | T | 9 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 10 | HG01099.hp1 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+132C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764275 | ||||||
chr16:764295
|
A | G | 105 | a0001c0001t0001g0070a0001c0001t0001g0241a0001c0001t0001g0242others(102): Show | 121 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.300+152A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764295 | ||||||
chr16:764307
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0223others(79): Show | 92 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.300+164G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764307 | ||||||
chr16:764354
|
T | A | 68 | a0001c0008t0001g0300a0001c0008t0001g0301a0001c0008t0001g0302others(65): Show | 79 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.300+211T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764354 | ||||||
chr16:764374
|
C | A | 1 | a0002c0025t0002g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300+231C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764374 | ||||||
chr16:764494
|
A | G | 134 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(131): Show | 151 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.301-153A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764494 | ||||||
chr16:764524
|
C | T | 8 | a0001c0001t0001g0005a0002c0003t0002g0247a0002c0003t0002g0248others(5): Show | 9 | HG01109.hp2 HG02109.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-123C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764524 | ||||||
chr16:764607
|
C | T | 1 | a0001c0022t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.301-40C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764607 | ||||||
chr16:764617
|
C | T | 3 | a0001c0022t0001g0270a0017c0023t0001g0020a0017c0023t0001g0021 | 3 | HG01099.hp1 HG01361.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.301-30C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764617 | ||||||
chr16:764742
|
T | A | 1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.380+16T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | chr16 | 764742 | ||||||
chr16:764749
|
AC | A | 30 | a0001c0001t0001g0179a0002c0015t0003g0255a0002c0015t0003g0256others(27): Show | 31 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.380+30delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 764749 | |||||
chr16:764754
|
C | T | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.380+28C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | chr16 | 764754 | ||||||
chr16:764756
|
C | A | 3 | a0007c0016t0001g0043a0007c0016t0005g0012a0007c0016t0005g0229 | 4 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+30C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | chr16 | 764756 | ||||||
chr16:765100
|
C | G | 1 | a0002c0034t0003g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.511-10C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 8/17 | chr16 | 765100 | ||||||
chr16:765350
|
T | C | 1 | a0007c0016t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.704+47T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765350 | ||||||
chr16:765370
|
T | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0223others(181): Show | 209 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.704+67T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765370 | ||||||
chr16:765379
|
T | C | 185 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0223others(182): Show | 210 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.704+76T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765379 | ||||||
chr16:765411
|
A | T | 1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.704+108A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765411 | ||||||
chr16:765413
|
C | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0223others(109): Show | 126 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.704+110C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765413 | ||||||
chr16:765416
|
C | T | 1 | a0006c0007t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.705-111C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765416 | ||||||
chr16:765628
|
A | G | 354 | a0000c0039t0008g0146a0001c0001t0001g0005a0001c0001t0001g0010others(351): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.795+11A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/17 | chr16 | 765628 | ||||||
chr16:765808
|
C | T | 1 | a0002c0002t0002g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.895+18C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 765808 | ||||||
chr16:765989
|
A | T | 1 | a0006c0010t0001g0239 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.896-70A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 765989 | ||||||
chr16:766012
|
G | C | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.896-47G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 766012 | ||||||
chr16:766020
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG00423.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.896-39C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 766020 | ||||||
chr16:766032
|
C | G | 2 | a0005c0005t0001g0027a0005c0005t0001g0041 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.896-27C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 766032 | ||||||
chr16:766287
|
C | T | 22 | a0001c0022t0001g0178a0001c0022t0001g0270a0004c0006t0001g0181others(19): Show | 22 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-48C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/17 | chr16 | 766287 | ||||||
chr16:766294
|
T | G | 182 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0222others(179): Show | 207 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.1075-41T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/17 | chr16 | 766294 | ||||||
chr16:766306
|
A | G | 1 | a0002c0034t0003g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1075-29A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/17 | chr16 | 766306 | ||||||
chr16:766499
|
C | T | 8 | a0002c0003t0002g0260a0002c0003t0004g0212a0002c0003t0004g0213others(5): Show | 8 | HG01934.hp2 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+9C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766499 | ||||||
chr16:766500
|
C | T | 21 | a0002c0003t0002g0253a0002c0015t0003g0066a0003c0004t0003g0002others(18): Show | 27 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+10C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766500 | ||||||
chr16:766506
|
G | T | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+16G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766506 | ||||||
chr16:766550
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1230+60G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766550 | ||||||
chr16:766618
|
A | C | 1 | a0006c0010t0001g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-50A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766618 | ||||||
chr16:766847
|
G | A | 1 | a0002c0002t0002g0299 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1373+37G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 14/17 | chr16 | 766847 | ||||||
chr16:766874
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1374-11C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 14/17 | chr16 | 766874 | ||||||
chr16:767016
|
AGCCAGGG others(8): Show |
A | 114 | a0001c0001t0001g0252a0002c0002t0002g0001a0002c0002t0002g0007others(111): Show | 131 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.1501+12_1501+26del others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 767016 | |||||
chr16:767024
|
A | T | 1 | a0009c0031t0002g0353 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1501+12A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767024 | ||||||
chr16:767025
|
GTCCCTGG others(7): Show |
G | 1 | a0009c0031t0002g0353 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1501+14_1501+27del others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767025 | ||||||
chr16:767071
|
C | A | 1 | a0002c0002t0002g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1501+59C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767071 | ||||||
chr16:767176
|
G | A | 2 | a0001c0022t0001g0270a0004c0006t0001g0240 | 2 | HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1501+164G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767176 | ||||||
chr16:767190
|
C | T | 10 | a0008c0009t0002g0028a0008c0009t0002g0044a0008c0009t0002g0045others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1501+178C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767190 | ||||||
chr16:767213
|
G | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0222others(102): Show | 123 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1502-163G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767213 | ||||||
chr16:767237
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1502-139C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767237 | ||||||
chr16:767238
|
G | C | 1 | a0001c0001t0001g0176 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1502-138G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767238 | ||||||
chr16:767241
|
T | C | 93 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0252others(90): Show | 109 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.1502-135T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767241 | ||||||
chr16:767262
|
ATCCCTAA others(9): Show |
A | 1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1502-113_1502-98de others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767262 | ||||||
chr16:767339
|
G | T | 89 | a0001c0001t0001g0252a0002c0002t0002g0001a0002c0002t0002g0007others(86): Show | 105 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.1502-37G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767339 | ||||||
chr16:767364
|
C | G | 1 | a0014c0047t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1502-12C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767364 | ||||||
chr16:767369
|
C | T | 1 | a0002c0003t0004g0211 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.1502-7C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767369 | ||||||
chr16:767481
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1596+11C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767481 | ||||||
chr16:767484
|
G | A | 5 | a0002c0003t0004g0211a0010c0013t0006g0209a0010c0013t0006g0210others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+14G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767484 | ||||||
chr16:767493
|
C | T | 17 | a0001c0001t0001g0252a0002c0003t0002g0260a0002c0003t0004g0211others(14): Show | 17 | HG00738.hp1 HG01934.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+23C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767493 | ||||||
chr16:767495
|
T | TGTGGAGG others(39): Show |
1 | a0005c0005t0009g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596+33_1596+78dup others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | |||||
chr16:767495
|
T | TGTGGAGG others(35): Show |
5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+32_1596+33ins others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | |||||
chr16:767495
|
T | TGTGGGGG others(34): Show |
1 | a0003c0004t0003g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596+29_1596+30ins others(41): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | |||||
chr16:767495
|
T | TGTGGGGG others(35): Show |
1 | a0003c0004t0003g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+29_1596+30ins others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | |||||
chr16:767502
|
G | GGGGGGGC others(36): Show |
1 | a0003c0004t0003g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1596+32_1596+33ins others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767502 | ||||||
chr16:767503
|
A | G | 2 | a0003c0004t0003g0269a0003c0004t0003g0278 | 2 | HG00423.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1596+33A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767503 | ||||||
chr16:767509
|
C | CCGTGGAG others(24): Show |
2 | a0005c0005t0001g0025a0005c0005t0001g0033 | 2 | NA18995.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1596+48_1596+78dup others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767509 | |||||
chr16:767509
|
C | G | 11 | a0001c0001t0001g0354a0001c0001t0001g0355a0002c0015t0003g0066others(8): Show | 15 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+39C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767509 | ||||||
chr16:767510
|
C | A | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+40C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767510 | ||||||
chr16:767515
|
A | AGGAGCCC others(4): Show |
1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+49_1596+50ins others(11): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767515 | |||||
chr16:767525
|
A | C | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+55A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767525 | ||||||
chr16:767525
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+55A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767525 | ||||||
chr16:767527
|
T | C | 8 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(5): Show | 12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+57T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767527 | ||||||
chr16:767527
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+57T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767527 | ||||||
chr16:767528
|
G | GGGGGGGT others(4): Show |
1 | a0001c0001t0001g0062 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+60_1596+61ins others(11): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767528 | |||||
chr16:767534
|
A | AGGGGCGT others(137): Show |
1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+70_1596+71ins others(144): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767534 | |||||
chr16:767540
|
G | A | 3 | a0012c0018t0001g0078a0012c0018t0001g0079a0012c0018t0001g0186 | 3 | HG01123.hp1 HG01256.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1596+70G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767540 | ||||||
chr16:767540
|
G | GCGTGGAG others(296): Show |
1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(303): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | |||||
chr16:767540
|
G | GCGTGGAG others(355): Show |
1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(362): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | |||||
chr16:767540
|
G | GCGTGGAG others(242): Show |
1 | a0017c0023t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(249): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | |||||
chr16:767540
|
G | GCGTGGAG others(302): Show |
1 | a0001c0001t0001g0349 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(309): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | |||||
chr16:767541
|
C | A | 8 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(5): Show | 12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+71C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767541 | ||||||
chr16:767541
|
C | T | 20 | a0001c0022t0001g0178a0001c0022t0001g0270a0004c0006t0001g0181others(17): Show | 20 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1596+71C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767541 | ||||||
chr16:767542
|
G | A | 1 | a0014c0047t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1596+72G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767542 | ||||||
chr16:767542
|
G | GC | 8 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(5): Show | 12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+72_1596+73ins others(1): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767542 | ||||||
chr16:767543
|
T | G | 8 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(5): Show | 12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+73T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767543 | ||||||
chr16:767546
|
A | AG | 50 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0071others(47): Show | 57 | HG00642.hp1 HG00673.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.1596+83dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | |||||
chr16:767546
|
A | AGGAGGGG others(109): Show |
1 | a0001c0001t0001g0062 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+78_1596+79ins others(116): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | |||||
chr16:767546
|
A | AGGGGGCC others(214): Show |
1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+81_1596+82ins others(221): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | |||||
chr16:767546
|
A | AGGGGGGA others(94): Show |
1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+82_1596+83ins others(101): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | |||||
chr16:767546
|
A | AGGGGGGG others(590): Show |
1 | a0002c0002t0002g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(597): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | |||||
chr16:767547
|
G | GGGGGGGG others(392): Show |
1 | a0001c0001t0001g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767547 | |||||
chr16:767547
|
G | GGGGGGGG others(602): Show |
1 | a0002c0003t0004g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(609): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767547 | |||||
chr16:767548
|
G | GGGGGGGC others(208): Show |
1 | a0003c0004t0003g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(215): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767548 | |||||
chr16:767549
|
G | A | 10 | a0001c0001t0001g0080a0002c0015t0003g0066a0002c0015t0003g0174others(7): Show | 14 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+79G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767549 | ||||||
chr16:767549
|
G | GGGGGGCG others(97): Show |
4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(104): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767549 | |||||
chr16:767549
|
G | GGGGGGCG others(82): Show |
4 | a0010c0013t0006g0209a0010c0013t0006g0210a0010c0013t0007g0207others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(89): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767549 | |||||
chr16:767552
|
G | GGCCAGTG others(125): Show |
1 | a0002c0002t0002g0307 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1596+84_1596+85ins others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767552
|
G | GGGCCAGT others(127): Show |
1 | a0002c0002t0002g0329 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767552
|
G | GGGCGAGT others(85): Show |
4 | a0004c0006t0001g0346a0004c0006t0001g0350a0004c0021t0001g0298others(1): Show | 4 | HG00558.hp1 HG02602.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767552
|
G | GGGCGAGT others(426): Show |
1 | a0001c0001t0001g0348 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(433): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767552
|
G | GGGCGAGT others(112): Show |
1 | a0003c0004t0003g0227 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(119): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767552
|
G | GGGGCCAG others(128): Show |
1 | a0002c0002t0002g0335 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(135): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767552
|
G | GGGGCGAG others(86): Show |
1 | a0004c0006t0001g0224 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(93): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | |||||
chr16:767553
|
G | GGCCAGTG others(8): Show |
44 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0017others(41): Show | 55 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | ||||||
chr16:767553
|
G | GGCGAGTG others(8): Show |
39 | a0001c0001t0001g0241a0001c0001t0001g0252a0001c0022t0001g0178others(36): Show | 40 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | ||||||
chr16:767553
|
G | GGGCCAGT others(9): Show |
7 | a0002c0002t0002g0197a0002c0002t0002g0331a0002c0002t0002g0332others(4): Show | 7 | HG01109.hp1 HG01978.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | ||||||
chr16:767553
|
G | GGGCGAGT others(9): Show |
2 | a0006c0007t0001g0026a0008c0009t0002g0047 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | ||||||
chr16:767553
|
G | GGTGAGTG others(8): Show |
1 | a0002c0003t0004g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | ||||||
chr16:767554
|
C | G | 5 | a0002c0003t0004g0220a0003c0004t0003g0276a0003c0004t0003g0352others(2): Show | 5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+84C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767554 | ||||||
chr16:767555
|
G | C | 108 | a0001c0001t0001g0166a0001c0001t0001g0241a0001c0001t0001g0252others(105): Show | 120 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.1596+85G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767555 | ||||||
chr16:767556
|
T | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0080others(41): Show | 53 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1596+86T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767556 | ||||||
chr16:767556
|
T | C | 24 | a0001c0001t0001g0082a0001c0001t0001g0242a0001c0001t0001g0243others(21): Show | 28 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1596+86T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767556 | ||||||
chr16:767556
|
T | G | 98 | a0001c0001t0001g0241a0001c0001t0001g0252a0001c0022t0001g0178others(95): Show | 110 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1596+86T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767556 | ||||||
chr16:767557
|
G | C | 1 | a0002c0003t0004g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1596+87G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767557 | ||||||
chr16:767558
|
T | A | 12 | a0001c0001t0001g0348a0002c0003t0004g0216a0002c0003t0004g0220others(9): Show | 12 | HG00558.hp1 HG01952.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+88T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767558 | ||||||
chr16:767558
|
T | C | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+88T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767558 | ||||||
chr16:767558
|
T | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0081others(4): Show | 7 | HG00280.hp1 HG02015.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+88T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767558 | ||||||
chr16:767558
|
T | TG | 11 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0086others(8): Show | 11 | HG00642.hp2 HG01175.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+95dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767558 | |||||
chr16:767559
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0081 | 3 | HG00280.hp1 HG02083.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1596+89G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767559 | ||||||
chr16:767559
|
G | GGAGGGGG others(71): Show |
1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1596+90_1596+91ins others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767559 | |||||
chr16:767560
|
G | GA | 15 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(12): Show | 19 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+90_1596+91ins others(1): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767560 | ||||||
chr16:767560
|
G | GAGGAGCC others(385): Show |
1 | a0002c0003t0004g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1596+90_1596+91ins others(392): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767560 | ||||||
chr16:767560
|
G | T | 5 | a0002c0003t0004g0220a0003c0004t0003g0276a0003c0004t0003g0352others(2): Show | 5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+90G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767560 | ||||||
chr16:767561
|
G | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(137): Show | 161 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1596+91G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767561 | ||||||
chr16:767561
|
G | GAGGAGGG others(147): Show |
1 | a0001c0001t0001g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1596+91_1596+92ins others(154): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767561 | ||||||
chr16:767561
|
G | GGGGGCGC others(16): Show |
1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1596+95_1596+96ins others(23): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767561 | |||||
chr16:767563
|
G | A | 5 | a0002c0003t0004g0220a0003c0004t0003g0276a0003c0004t0003g0352others(2): Show | 5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+93G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767563 | ||||||
chr16:767564
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(38): Show | 50 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.1596+94G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767564 | ||||||
chr16:767565
|
GT | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(39): Show | 51 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.1596+96delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767565 | ||||||
chr16:767566
|
T | A | 5 | a0002c0003t0004g0220a0003c0004t0003g0276a0003c0004t0003g0352others(2): Show | 5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+96T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767566 | ||||||
chr16:767566
|
T | C | 113 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(110): Show | 125 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1596+96T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767566 | ||||||
chr16:767566
|
T | G | 2 | a0001c0001t0001g0288a0002c0003t0004g0219 | 2 | HG01433.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1596+96T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767566 | ||||||
chr16:767566
|
T | TGCGTGGA others(8): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0035t0001g0206others(1): Show | 4 | HG00099.hp1 HG02015.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+121_1596+135d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | |||||
chr16:767566
|
T | TGCGTGGA others(405): Show |
1 | a0001c0001t0001g0100 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1596+135_1596+136i others(414): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | |||||
chr16:767566
|
T | TGCGTGGA others(390): Show |
1 | a0001c0001t0001g0151 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1596+163_1596+164i others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | |||||
chr16:767566
|
T | TGCGTGGA others(954): Show |
1 | a0005c0005t0001g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(963): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | |||||
chr16:767566
|
T | TGCGTGGA others(399): Show |
1 | a0005c0005t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+120_1596+121i others(408): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | |||||
chr16:767567
|
G | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(38): Show | 50 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.1596+97G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767567 | ||||||
chr16:767567
|
G | GC | 5 | a0002c0003t0004g0220a0003c0004t0003g0276a0003c0004t0003g0352others(2): Show | 5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+98dupC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767567 | |||||
chr16:767568
|
C | A | 2 | a0003c0004t0003g0269a0004c0006t0001g0262 | 2 | HG00423.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1596+98C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767568 | ||||||
chr16:767569
|
G | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(43): Show | 55 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+99G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767569 | ||||||
chr16:767570
|
T | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(43): Show | 55 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+100T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767570 | ||||||
chr16:767570
|
T | G | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+100T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767570 | ||||||
chr16:767573
|
A | AGGAGCCC others(4): Show |
1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1596+107_1596+108i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767573 | |||||
chr16:767573
|
A | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(43): Show | 55 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+103A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767573 | ||||||
chr16:767574
|
G | GGGGGGAG others(54): Show |
1 | a0024c0040t0001g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1596+105_1596+106i others(63): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767574 | |||||
chr16:767575
|
GA | G | 5 | a0002c0002t0002g0307a0002c0002t0002g0329a0002c0002t0002g0335others(2): Show | 5 | HG02015.hp2 HG02132.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+106delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767575 | ||||||
chr16:767576
|
A | AGGGGCGC others(445): Show |
1 | a0029c0046t0001g0034 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(454): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767576 | |||||
chr16:767576
|
A | AGGGGCGT others(7): Show |
1 | a0001c0001t0001g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1596+112_1596+113i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767576 | |||||
chr16:767576
|
A | T | 3 | a0001c0038t0001g0083a0012c0018t0001g0186a0024c0040t0001g0287 | 3 | HG01099.hp2 HG01123.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1596+106A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767576 | ||||||
chr16:767580
|
G | GCGCGTGG others(61): Show |
1 | a0002c0002t0002g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+123_1596+124i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767580 | |||||
chr16:767581
|
C | CGCGTGGA others(100): Show |
1 | a0001c0001t0001g0062 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+123_1596+124i others(109): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | |||||
chr16:767581
|
C | CGCGTGGA others(16): Show |
6 | a0001c0001t0001g0056a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG01169.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+120_1596+121i others(25): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | |||||
chr16:767581
|
C | CGCGTGGA others(165): Show |
1 | a0001c0001t0001g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1596+120_1596+121i others(174): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | |||||
chr16:767581
|
C | CGCGTGGA others(164): Show |
1 | a0001c0001t0001g0085 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1596+120_1596+121i others(173): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | |||||
chr16:767581
|
C | CGCGTGGA others(163): Show |
1 | a0001c0001t0001g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | |||||
chr16:767581
|
C | G | 3 | a0001c0038t0001g0083a0012c0018t0001g0186a0024c0040t0001g0287 | 3 | HG01099.hp2 HG01123.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1596+111C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767581 | ||||||
chr16:767582
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG02723.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+112G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767582 | ||||||
chr16:767582
|
G | C | 4 | a0006c0010t0001g0013a0006c0010t0001g0237a0006c0010t0001g0238others(1): Show | 5 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+112G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767582 | ||||||
chr16:767583
|
C | CGTGGAGG others(186): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(195): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767583 | |||||
chr16:767583
|
C | CGTGGAGG others(588): Show |
1 | a0001c0001t0001g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1596+120_1596+121i others(597): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767583 | |||||
chr16:767585
|
T | TGGAGGAG others(9): Show |
1 | a0001c0001t0001g0092 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1596+127_1596+128i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767585 | |||||
chr16:767587
|
GA | G | 15 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(12): Show | 19 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+118delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767587 | ||||||
chr16:767588
|
A | G | 1 | a0002c0015t0003g0066 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1596+118A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767588 | ||||||
chr16:767590
|
G | GGGGCCGT others(111): Show |
1 | a0001c0001t0001g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767590 | ||||||
chr16:767590
|
G | GGGGCCGT others(1421): Show |
1 | a0002c0003t0001g0159 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(1430): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767590 | ||||||
chr16:767591
|
A | AGGAGGGG others(21): Show |
1 | a0001c0001t0001g0349 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1596+123_1596+124i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767591 | |||||
chr16:767591
|
A | AGGAGGGG others(121): Show |
1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+123_1596+124i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767591 | |||||
chr16:767591
|
A | AGGAGGGG others(162): Show |
1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1596+123_1596+124i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767591 | |||||
chr16:767591
|
A | G | 24 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0242others(21): Show | 28 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1596+121A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767591 | ||||||
chr16:767596
|
C | CGAGCGGG others(53): Show |
4 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0228others(1): Show | 4 | HG02451.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+127_1596+128i others(62): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767596 | |||||
chr16:767596
|
C | G | 3 | a0001c0001t0001g0179a0002c0003t0001g0159a0017c0023t0001g0020 | 3 | HG00735.hp2 HG01099.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1596+126C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767596 | ||||||
chr16:767596
|
C | T | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+126C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767596 | ||||||
chr16:767596
|
CGCGTGGA others(5): Show |
C | 1 | a0006c0010t0001g0236 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1596+128_1596+139d others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767596 | |||||
chr16:767597
|
G | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | NA18953.hp1 NA19002.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+127G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767597 | ||||||
chr16:767597
|
G | GAGCGGGA others(9): Show |
3 | a0006c0007t0001g0014a0006c0007t0001g0026a0006c0007t0001g0258 | 4 | HG01069.hp2 HG01071.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+127_1596+128i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767597 | ||||||
chr16:767598
|
C | A | 69 | a0001c0001t0001g0241a0001c0022t0001g0178a0002c0002t0002g0001others(66): Show | 81 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1596+128C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | ||||||
chr16:767598
|
C | CATGGGGG others(3): Show |
1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+128_1596+129i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | ||||||
chr16:767598
|
C | CGTGGAGG others(132): Show |
1 | a0002c0002t0002g0307 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1596+138_1596+139i others(141): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767598 | |||||
chr16:767598
|
C | CGTGGGGG others(3): Show |
1 | a0001c0001t0001g0158 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1596+132_1596+133i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767598 | |||||
chr16:767598
|
C | G | 2 | a0002c0015t0003g0256a0014c0047t0003g0030 | 2 | HG03579.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1596+128C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | ||||||
chr16:767598
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01099.hp1 HG02897.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+128C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | ||||||
chr16:767599
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+129G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767599 | ||||||
chr16:767599
|
G | GC | 64 | a0001c0001t0001g0241a0001c0022t0001g0178a0002c0002t0002g0001others(61): Show | 75 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1596+129_1596+130i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767599 | ||||||
chr16:767600
|
T | A | 2 | a0002c0015t0003g0256a0014c0047t0003g0030 | 2 | HG03579.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1596+130T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767600 | ||||||
chr16:767600
|
T | G | 64 | a0001c0001t0001g0241a0001c0022t0001g0178a0002c0002t0002g0001others(61): Show | 75 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1596+130T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767600 | ||||||
chr16:767600
|
T | TGGA | 32 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0223others(29): Show | 36 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1596+133_1596+135d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767600 | |||||
chr16:767600
|
TGGAGGG | T | 4 | a0006c0010t0001g0013a0006c0010t0001g0237a0006c0010t0001g0238others(1): Show | 5 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+133_1596+138d others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767600 | |||||
chr16:767603
|
A | AG | 8 | a0001c0001t0001g0060a0001c0001t0001g0072a0001c0001t0001g0157others(5): Show | 8 | HG01952.hp2 HG02056.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+139dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767603 | |||||
chr16:767604
|
GGGGGGAG others(1): Show |
G | 5 | a0001c0001t0001g0166a0007c0016t0001g0043a0007c0016t0005g0012others(2): Show | 6 | HG01070.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+136_1596+143d others(10): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767604 | |||||
chr16:767605
|
G | GA | 92 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0094others(89): Show | 107 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1596+135_1596+136i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | ||||||
chr16:767605
|
G | GAGGA | 5 | a0004c0006t0001g0224a0004c0006t0001g0346a0004c0006t0001g0350others(2): Show | 5 | HG00558.hp1 HG02602.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+135_1596+136i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | ||||||
chr16:767605
|
G | GAGGGGCG others(41): Show |
8 | a0002c0002t0002g0310a0008c0009t0002g0028a0008c0009t0002g0044others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+135_1596+136i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | ||||||
chr16:767605
|
G | GAGGGGCG others(72): Show |
1 | a0014c0024t0002g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1596+135_1596+136i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | ||||||
chr16:767606
|
G | A | 9 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(6): Show | 9 | HG02055.hp2 HG02155.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+136G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767606 | ||||||
chr16:767608
|
G | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0223others(31): Show | 38 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596+138G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767608 | ||||||
chr16:767609
|
G | C | 13 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0104others(10): Show | 13 | HG01123.hp1 HG01169.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+139G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767609 | ||||||
chr16:767610
|
A | C | 152 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0062others(149): Show | 171 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1596+140A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767610 | ||||||
chr16:767610
|
A | G | 1 | a0008c0009t0002g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+140A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767610 | ||||||
chr16:767611
|
G | A | 62 | a0001c0001t0001g0241a0001c0022t0001g0178a0002c0002t0002g0001others(59): Show | 73 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1596+141G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767611 | ||||||
chr16:767611
|
GC | G | 4 | a0006c0010t0001g0013a0006c0010t0001g0237a0006c0010t0001g0238others(1): Show | 5 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+142delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767611 | ||||||
chr16:767612
|
C | CGGGAG | 19 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0223others(16): Show | 21 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1596+143_1596+144i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767612 | |||||
chr16:767612
|
C | T | 20 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0082others(17): Show | 22 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596+142C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767612 | ||||||
chr16:767613
|
G | A | 6 | a0003c0004t0003g0227a0004c0006t0001g0224a0004c0006t0001g0346others(3): Show | 6 | HG00558.hp1 HG02602.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+143G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | ||||||
chr16:767613
|
G | GAGCGGGA others(46): Show |
1 | a0008c0009t0002g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+143_1596+144i others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | ||||||
chr16:767613
|
G | GGGA | 13 | a0002c0003t0002g0247a0002c0003t0002g0248a0002c0003t0002g0249others(10): Show | 15 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+143_1596+144i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | ||||||
chr16:767613
|
GTGGGGGG others(3): Show |
G | 1 | a0006c0010t0001g0236 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1596+144_1596+153d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | ||||||
chr16:767614
|
T | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(26): Show | 33 | HG00642.hp1 HG01069.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1596+144T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767614 | ||||||
chr16:767614
|
T | C | 1 | a0008c0009t0002g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+144T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767614 | ||||||
chr16:767614
|
T | G | 14 | a0002c0003t0002g0247a0002c0003t0002g0248a0002c0003t0002g0249others(11): Show | 16 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+144T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767614 | ||||||
chr16:767614
|
T | TG | 21 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0104others(18): Show | 21 | HG00558.hp1 HG01123.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1596+150dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAC | 11 | a0002c0002t0002g0310a0002c0003t0004g0212a0002c0003t0004g0215others(8): Show | 11 | HG01891.hp2 HG01978.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+146_1596+147i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGAG others(198): Show |
1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(207): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGAG others(40): Show |
2 | a0003c0004t0003g0273a0003c0004t0003g0291 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGAG others(106): Show |
2 | a0010c0013t0006g0209a0010c0013t0006g0210 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(115): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGAG others(108): Show |
2 | a0010c0013t0007g0207a0010c0013t0007g0208 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(117): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(8): Show |
1 | a0001c0001t0001g0094 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1596+146_1596+147i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(351): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG02257.hp1 HG03130.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(360): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(352): Show |
1 | a0001c0001t0001g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(361): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(425): Show |
1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(434): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(273): Show |
1 | a0002c0003t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(282): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(486): Show |
1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+146_1596+147i others(495): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGAGGGG others(384): Show |
1 | a0025c0042t0001g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(393): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGGGGGC others(521): Show |
1 | a0001c0001t0001g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(530): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGGGGGC others(492): Show |
1 | a0005c0005t0001g0037 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(501): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767614
|
T | TGGGGGGC others(557): Show |
1 | a0005c0005t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(566): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | |||||
chr16:767616
|
G | A | 13 | a0002c0003t0002g0247a0002c0003t0002g0248a0002c0003t0002g0249others(10): Show | 15 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+146G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767616 | ||||||
chr16:767616
|
G | GAGGA | 72 | a0001c0001t0001g0241a0001c0001t0001g0252a0001c0022t0001g0178others(69): Show | 87 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.1596+146_1596+147i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767616 | ||||||
chr16:767617
|
G | A | 14 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0179others(11): Show | 18 | HG00639.hp1 HG01891.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+147G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767617 | ||||||
chr16:767617
|
G | C | 8 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(5): Show | 8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+147G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767617 | ||||||
chr16:767619
|
G | A | 8 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(5): Show | 8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+149G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
G | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0086others(39): Show | 46 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.1596+149G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
G | GAGGAGGG others(148): Show |
2 | a0002c0002t0002g0329a0002c0002t0002g0335 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1596+149_1596+150i others(157): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
G | GAGGGGCG others(80): Show |
6 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(3): Show | 10 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+149_1596+150i others(89): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
G | GCGTGGAG others(112): Show |
1 | a0001c0001t0001g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+149_1596+150i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
G | GGCGTGGA others(344): Show |
1 | a0001c0001t0001g0199 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1596+167_1596+168i others(353): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(217): Show |
2 | a0001c0001t0001g0104a0001c0038t0001g0083 | 2 | HG02129.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1596+176_1596+177i others(226): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(314): Show |
1 | a0009c0011t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1596+191_1596+192i others(323): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(324): Show |
1 | a0001c0001t0001g0176 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(333): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(290): Show |
1 | a0001c0001t0001g0351 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(299): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(1370): Show |
1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1379): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(275): Show |
1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(284): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(382): Show |
1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(391): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(149): Show |
1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(158): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(1105): Show |
1 | a0001c0001t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1114): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(1745): Show |
1 | a0001c0001t0001g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1754): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(321): Show |
1 | a0001c0001t0001g0112 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(330): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(335): Show |
1 | a0001c0008t0001g0300 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(344): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(782): Show |
1 | a0001c0001t0001g0070 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(791): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(338): Show |
1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(347): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(294): Show |
1 | a0001c0001t0001g0114 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(303): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(358): Show |
1 | a0005c0005t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(367): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(363): Show |
1 | a0005c0005t0009g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(372): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(518): Show |
1 | a0001c0001t0001g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(527): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(336): Show |
1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(345): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(337): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0200 | 2 | HG02129.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(346): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(352): Show |
1 | a0001c0001t0001g0120 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(361): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(604): Show |
1 | a0023c0037t0001g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(613): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(337): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18940.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(346): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(338): Show |
1 | a0012c0018t0001g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(347): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(1350): Show |
1 | a0001c0001t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1359): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(493): Show |
2 | a0001c0001t0001g0127a0001c0001t0005g0221 | 2 | HG01975.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(502): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(821): Show |
1 | a0026c0030t0001g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(830): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(919): Show |
1 | a0001c0001t0001g0347 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(928): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(620): Show |
1 | a0001c0001t0001g0092 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(629): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(2451): Show |
1 | a0001c0001t0001g0133 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(2460): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(319): Show |
1 | a0009c0011t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(328): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(362): Show |
1 | a0001c0001t0011g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(371): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(732): Show |
1 | a0001c0001t0001g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(741): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(336): Show |
1 | a0001c0001t0001g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(345): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(342): Show |
1 | a0009c0011t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(351): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(610): Show |
1 | a0001c0001t0001g0069 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(619): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(385): Show |
1 | a0001c0001t0001g0137 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(394): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(505): Show |
1 | a0001c0001t0001g0138 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(514): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(590): Show |
1 | a0001c0001t0001g0139 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(599): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(474): Show |
1 | a0001c0001t0001g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(483): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(210): Show |
1 | a0004c0017t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(219): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(495): Show |
1 | a0001c0008t0001g0302 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(504): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(502): Show |
1 | a0001c0008t0001g0304 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(511): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(346): Show |
1 | a0001c0001t0001g0143 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(355): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(497): Show |
1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(506): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(389): Show |
1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(398): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(420): Show |
1 | a0001c0001t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(429): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(428): Show |
1 | a0030c0048t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(437): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(366): Show |
1 | a0027c0026t0001g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(375): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(140): Show |
1 | a0005c0005t0001g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(149): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(301): Show |
1 | a0000c0039t0008g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(310): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(1390): Show |
1 | a0001c0001t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596+170_1596+171i others(1399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(270): Show |
1 | a0001c0001t0001g0105 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(279): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(364): Show |
1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(373): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(299): Show |
1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1596+165_1596+166i others(308): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(371): Show |
1 | a0001c0001t0001g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(380): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(340): Show |
1 | a0001c0001t0001g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1596+163_1596+164i others(349): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(338): Show |
1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(347): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(353): Show |
1 | a0001c0001t0001g0341 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(362): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(147): Show |
1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1596+158_1596+159i others(156): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGCGTGGA others(425): Show |
1 | a0005c0005t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1596+158_1596+159i others(434): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGGCGTGG others(39): Show |
1 | a0001c0001t0001g0349 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1596+150_1596+151i others(48): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGGGCGCA others(169): Show |
1 | a0002c0003t0004g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1596+150_1596+151i others(178): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGGTGTGG others(59): Show |
1 | a0003c0004t0003g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596+150_1596+151i others(68): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGGTGTGG others(72): Show |
1 | a0001c0001t0001g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1596+150_1596+151i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GGGTGTGG others(58): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1596+150_1596+151i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
G | GTGTGTGG others(48): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0158 | 2 | NA18952.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1596+149_1596+150i others(57): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
G | T | 13 | a0002c0002t0002g0310a0002c0003t0004g0212a0002c0003t0004g0215others(10): Show | 13 | HG01891.hp2 HG01978.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+149G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | ||||||
chr16:767619
|
GGCGTGGA others(8): Show |
G | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1596+174_1596+188d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
GGCGTGGA others(127): Show |
G | 2 | a0001c0001t0001g0354a0011c0014t0001g0003 | 4 | HG00140.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+174_1596+307d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767619
|
GGCGTGGA others(314): Show |
G | 1 | a0001c0008t0001g0301 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1596+174_1597-415d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | |||||
chr16:767620
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0022t0001g0270others(4): Show | 8 | HG01109.hp2 HG01361.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+150G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767620 | ||||||
chr16:767620
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1596+150G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767620 | ||||||
chr16:767620
|
G | GCGTGGAG others(475): Show |
1 | a0001c0001t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(484): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767620 | |||||
chr16:767620
|
G | GGGCGCAT others(91): Show |
1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1596+150_1596+151i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767620 | ||||||
chr16:767621
|
C | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0154a0002c0003t0004g0216 | 3 | HG01952.hp2 HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+151C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767621 | ||||||
chr16:767621
|
C | T | 9 | a0001c0001t0001g0180a0003c0004t0003g0227a0003c0004t0003g0273others(6): Show | 9 | HG00558.hp1 HG02486.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+151C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767621 | ||||||
chr16:767622
|
G | GAGC | 86 | a0001c0001t0001g0241a0001c0001t0001g0252a0001c0022t0001g0178others(83): Show | 103 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.1596+152_1596+153i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767622 | ||||||
chr16:767622
|
G | GTGGAGGA others(337): Show |
1 | a0001c0001t0001g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(346): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767622 | |||||
chr16:767622
|
GT | G | 8 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(5): Show | 8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+153delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767622 | ||||||
chr16:767623
|
T | A | 1 | a0004c0017t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1596+153T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767623 | ||||||
chr16:767623
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0154a0002c0003t0004g0216 | 3 | HG01952.hp2 HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+153T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767623 | ||||||
chr16:767623
|
T | G | 88 | a0001c0001t0001g0067a0001c0001t0001g0241a0001c0001t0001g0252others(85): Show | 105 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.1596+153T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767623 | ||||||
chr16:767624
|
G | C | 1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+154G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767624 | ||||||
chr16:767625
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0154 | 2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+155G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767625 | ||||||
chr16:767626
|
A | C | 1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+156A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767626 | ||||||
chr16:767626
|
AGG | A | 5 | a0002c0003t0004g0230a0002c0003t0004g0231a0002c0003t0004g0232others(2): Show | 5 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+157_1596+158d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767626 | ||||||
chr16:767627
|
G | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0154 | 2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+157G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767627 | ||||||
chr16:767627
|
GGA | G | 9 | a0001c0001t0001g0081a0001c0001t0001g0156a0001c0001t0001g0179others(6): Show | 10 | HG01069.hp2 HG01071.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+159_1596+160d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767627 | |||||
chr16:767627
|
GGAGGGGC others(71): Show |
G | 1 | a0012c0018t0001g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1596+159_1596+236d others(80): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767627 | |||||
chr16:767628
|
G | T | 1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+158G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767628 | ||||||
chr16:767628
|
GA | G | 13 | a0002c0002t0002g0322a0003c0004t0003g0227a0003c0004t0003g0269others(10): Show | 13 | HG00423.hp2 HG00558.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+159delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767628 | ||||||
chr16:767629
|
A | AGGGGCGC others(374): Show |
1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(383): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(604): Show |
1 | a0001c0001t0001g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(613): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(83): Show |
1 | a0001c0001t0001g0355 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(481): Show |
1 | a0001c0035t0001g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(490): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(420): Show |
1 | a0005c0005t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(429): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(548): Show |
1 | a0005c0005t0001g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(557): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(349): Show |
1 | a0005c0005t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(358): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(496): Show |
1 | a0001c0001t0001g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(505): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(470): Show |
1 | a0012c0018t0001g0078 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(479): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(626): Show |
1 | a0001c0001t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(635): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGC others(551): Show |
1 | a0011c0014t0001g0145 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(560): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGCGT others(681): Show |
1 | a0005c0005t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(690): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | AGGGGTGC others(17): Show |
1 | a0001c0001t0001g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | |||||
chr16:767629
|
A | C | 5 | a0002c0003t0004g0230a0002c0003t0004g0231a0002c0003t0004g0232others(2): Show | 5 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+159A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767629 | ||||||
chr16:767629
|
A | G | 10 | a0001c0001t0001g0071a0001c0001t0001g0154a0001c0001t0001g0223others(7): Show | 11 | HG01099.hp1 HG01952.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+159A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767629 | ||||||
chr16:767629
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1596+159A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767629 | ||||||
chr16:767632
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+162G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767632 | ||||||
chr16:767633
|
G | GCGCGTGG others(166): Show |
3 | a0001c0001t0001g0091a0001c0001t0001g0201a0009c0011t0001g0340 | 3 | NA19002.hp1 NA19083.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | |||||
chr16:767633
|
G | GCGCGTGG others(732): Show |
1 | a0001c0001t0001g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(741): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | |||||
chr16:767633
|
G | GCGCGTGG others(166): Show |
1 | a0001c0001t0001g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | |||||
chr16:767633
|
G | GCGCGTGG others(138): Show |
1 | a0001c0008t0001g0303 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(147): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | |||||
chr16:767633
|
G | GCGCGTGG others(168): Show |
1 | a0001c0001t0001g0339 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(177): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | |||||
chr16:767633
|
G | GTGCGTGG others(166): Show |
1 | a0001c0041t0001g0152 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767633 | ||||||
chr16:767633
|
G | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0156a0001c0001t0001g0179others(1): Show | 4 | HG02083.hp2 HG02602.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+163G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767633 | ||||||
chr16:767634
|
C | CGAGCGGG others(38): Show |
1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(47): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGAGCGGG others(22): Show |
3 | a0002c0003t0002g0248a0002c0003t0002g0249a0002c0003t0004g0211 | 3 | HG02647.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1596+165_1596+166i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(6): Show |
6 | a0002c0002t0002g0007a0002c0002t0002g0054a0002c0002t0002g0328others(3): Show | 8 | HG00733.hp2 HG01109.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+171_1596+172i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(138): Show |
2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+176_1596+177i others(147): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(269): Show |
1 | a0001c0001t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596+176_1596+177i others(278): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(17): Show |
5 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(2): Show | 5 | HG03492.hp1 HG03710.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+173_1596+174i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(591): Show |
1 | a0005c0005t0001g0036 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(600): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(363): Show |
1 | a0001c0001t0001g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(372): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(286): Show |
1 | a0001c0001t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(295): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(518): Show |
1 | a0001c0001t0001g0286 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(527): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(492): Show |
1 | a0001c0001t0001g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(501): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(307): Show |
1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(316): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(444): Show |
1 | a0001c0001t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(453): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(1853): Show |
1 | a0001c0001t0001g0132 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1862): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(513): Show |
1 | a0002c0003t0001g0059 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(522): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(537): Show |
1 | a0001c0001t0001g0077 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(546): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(353): Show |
1 | a0001c0001t0001g0072 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(362): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(16): Show |
2 | a0001c0008t0001g0305a0001c0008t0001g0306 | 2 | NA18939.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(25): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGCGTGGA others(111): Show |
1 | a0001c0001t0001g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | CGTGTGGA others(253): Show |
1 | a0001c0001t0001g0163 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(262): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | |||||
chr16:767634
|
C | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0150others(2): Show | 5 | HG00558.hp2 HG01952.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+164C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767634 | ||||||
chr16:767634
|
C | T | 10 | a0002c0003t0004g0230a0002c0003t0004g0231a0002c0003t0004g0232others(7): Show | 11 | HG01069.hp2 HG01071.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+164C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767634 | ||||||
chr16:767635
|
G | A | 13 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(10): Show | 17 | HG01099.hp1 HG02055.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+165G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767635 | ||||||
chr16:767636
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0166others(14): Show | 20 | HG01070.hp1 HG01109.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1596+166C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | ||||||
chr16:767636
|
C | CATGGGGG others(3): Show |
1 | a0004c0017t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1596+166_1596+167i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | ||||||
chr16:767636
|
C | CGTGGAGG others(163): Show |
1 | a0001c0001t0010g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767636 | |||||
chr16:767636
|
C | G | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+166C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | ||||||
chr16:767636
|
C | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0160others(3): Show | 6 | HG00609.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+166C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | ||||||
chr16:767637
|
G | GC | 16 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0022t0001g0270others(13): Show | 19 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+167_1596+168i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767637 | ||||||
chr16:767638
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+168T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767638 | ||||||
chr16:767638
|
T | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0022t0001g0270others(13): Show | 19 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+168T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767638 | ||||||
chr16:767639
|
GGA | G | 7 | a0008c0009t0002g0028a0008c0009t0002g0044a0008c0009t0002g0045others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+171_1596+172d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767639 | |||||
chr16:767640
|
GA | G | 5 | a0002c0003t0004g0212a0002c0003t0004g0214a0006c0010t0001g0236others(2): Show | 5 | HG01978.hp1 HG02055.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+171delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767640 | ||||||
chr16:767641
|
A | AGGGGGCC others(225): Show |
1 | a0001c0001t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(234): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767641 | |||||
chr16:767641
|
A | AGGGGGCC others(242): Show |
1 | a0001c0001t0001g0122 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(251): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767641 | |||||
chr16:767641
|
A | G | 1 | a0002c0003t0004g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1596+171A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767641 | ||||||
chr16:767641
|
AGG | A | 46 | a0002c0002t0002g0001a0002c0002t0002g0017a0002c0002t0002g0018others(43): Show | 55 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+172_1596+173d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767641 | ||||||
chr16:767642
|
G | GGGGGCCG others(3): Show |
1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGCCG others(125): Show |
1 | a0001c0001t0001g0130 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGCCG others(360): Show |
1 | a0001c0001t0001g0285 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(369): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGCCG others(1467): Show |
1 | a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(1476): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGCCG others(111): Show |
1 | a0001c0001t0001g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGCCG others(286): Show |
1 | a0001c0001t0001g0172 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(295): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGCCG others(383): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(392): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
G | GGGGGGCC others(47): Show |
1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(56): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767642
|
GGA | G | 16 | a0001c0001t0001g0241a0002c0002t0002g0310a0002c0015t0003g0255others(13): Show | 18 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+174_1596+175d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | |||||
chr16:767643
|
G | GGGGCCGT others(45): Show |
1 | a0005c0005t0001g0033 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767643 | ||||||
chr16:767643
|
GA | G | 16 | a0001c0001t0001g0071a0001c0001t0001g0090a0001c0001t0001g0094others(13): Show | 16 | HG00544.hp2 HG00609.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+174delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767643 | ||||||
chr16:767644
|
A | AGGAGGGG others(20): Show |
1 | a0002c0002t0002g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+176_1596+177i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767644 | |||||
chr16:767644
|
A | AGGAGGGG others(224): Show |
1 | a0002c0003t0004g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1596+176_1596+177i others(233): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767644 | |||||
chr16:767644
|
A | C | 46 | a0002c0002t0002g0001a0002c0002t0002g0017a0002c0002t0002g0018others(43): Show | 55 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+174A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767644 | ||||||
chr16:767644
|
A | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0060a0001c0001t0001g0087others(28): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1596+174A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767644 | ||||||
chr16:767648
|
G | C | 5 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0195others(2): Show | 5 | HG00544.hp2 HG01081.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+178G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767648 | ||||||
chr16:767649
|
C | CGTGTGGG others(5): Show |
1 | a0017c0023t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+180_1596+181i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767649 | |||||
chr16:767649
|
C | G | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0005c0005t0001g0025others(1): Show | 4 | NA18966.hp1 NA18995.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+179C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767649 | ||||||
chr16:767649
|
C | T | 60 | a0001c0001t0001g0071a0001c0001t0001g0154a0001c0001t0001g0241others(57): Show | 71 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.1596+179C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767649 | ||||||
chr16:767649
|
CGCGTGGA others(5): Show |
C | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+181_1596+192d others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767649 | |||||
chr16:767650
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0122a0007c0016t0001g0043others(3): Show | 7 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+180G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767650 | ||||||
chr16:767651
|
C | A | 10 | a0001c0001t0001g0222a0002c0002t0002g0295a0002c0003t0002g0253others(7): Show | 14 | HG02055.hp1 HG02155.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+181C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767651 | ||||||
chr16:767651
|
C | CGTGGGGG others(3): Show |
2 | a0002c0002t0002g0329a0002c0002t0002g0335 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1596+185_1596+186i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767651 | |||||
chr16:767651
|
C | T | 13 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0116others(10): Show | 13 | HG00544.hp2 HG00558.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+181C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767651 | ||||||
chr16:767652
|
G | A | 2 | a0001c0001t0001g0244a0004c0017t0001g0264 | 2 | HG03195.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1596+182G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767652 | ||||||
chr16:767652
|
G | GC | 7 | a0002c0002t0002g0295a0002c0003t0002g0253a0007c0012t0001g0004others(4): Show | 11 | HG02055.hp1 HG02155.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+182_1596+183i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767652 | ||||||
chr16:767653
|
T | G | 7 | a0002c0002t0002g0295a0002c0003t0002g0253a0007c0012t0001g0004others(4): Show | 11 | HG02055.hp1 HG02155.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+183T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767653 | ||||||
chr16:767654
|
GGAGGGGG others(6): Show |
G | 3 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0195 | 3 | HG00544.hp2 HG01081.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1596+186_1596+198d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767654 | |||||
chr16:767654
|
GGAGGGGG others(125): Show |
G | 1 | a0001c0001t0001g0279 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1596+186_1596+317d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767654 | |||||
chr16:767655
|
GA | G | 7 | a0001c0001t0001g0106a0001c0001t0001g0160a0001c0001t0001g0162others(4): Show | 8 | HG01981.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+186delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767655 | ||||||
chr16:767655
|
GAGGGGGG others(124): Show |
G | 1 | a0002c0003t0001g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1596+186_1596+316d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767655 | ||||||
chr16:767656
|
A | ACGGGGTG others(7): Show |
1 | a0002c0003t0002g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1596+186_1596+187i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767656 | ||||||
chr16:767656
|
A | AG | 9 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0108others(6): Show | 9 | HG00408.hp1 HG01175.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+192dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767656 | |||||
chr16:767656
|
A | G | 23 | a0001c0001t0001g0103a0001c0001t0001g0223a0001c0001t0001g0244others(20): Show | 26 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+186A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767656 | ||||||
chr16:767657
|
G | A | 1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+187G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767657 | ||||||
chr16:767657
|
G | C | 1 | a0002c0002t0002g0055 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1596+187G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767657 | ||||||
chr16:767657
|
G | T | 1 | a0005c0005t0001g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1596+187G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767657 | ||||||
chr16:767657
|
GGGGGGAG others(3): Show |
G | 3 | a0006c0010t0001g0236a0007c0016t0001g0043a0017c0023t0001g0021 | 3 | HG02280.hp2 HG02615.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1596+193_1596+202d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767657 | |||||
chr16:767657
|
GGGGGGAG others(122): Show |
G | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+193_1596+321d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767657 | |||||
chr16:767658
|
G | A | 1 | a0002c0003t0002g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1596+188G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | ||||||
chr16:767658
|
G | C | 1 | a0008c0009t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1596+188G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | ||||||
chr16:767658
|
G | GA | 83 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0115others(80): Show | 99 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.1596+188_1596+189i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | ||||||
chr16:767658
|
G | GAGGA | 9 | a0001c0001t0001g0355a0002c0002t0002g0310a0004c0006t0001g0224others(6): Show | 9 | HG00558.hp1 HG00642.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+188_1596+189i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | ||||||
chr16:767658
|
GGGGGAGC others(40): Show |
G | 2 | a0001c0001t0001g0071a0001c0001t0001g0154 | 2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+193_1596+239d others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767658 | |||||
chr16:767659
|
G | A | 1 | a0017c0023t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+189G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767659 | ||||||
chr16:767660
|
G | GTCGCGT | 3 | a0003c0004t0003g0227a0003c0004t0003g0273a0003c0004t0003g0291 | 3 | HG02486.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+190_1596+191i others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767660 | ||||||
chr16:767662
|
G | C | 18 | a0001c0001t0001g0042a0001c0001t0001g0081a0001c0001t0001g0091others(15): Show | 19 | HG00099.hp1 HG01952.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+192G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767662 | ||||||
chr16:767662
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+192G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767662 | ||||||
chr16:767663
|
A | C | 189 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0073others(186): Show | 214 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.1596+193A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767663 | ||||||
chr16:767663
|
A | G | 2 | a0001c0001t0001g0244a0005c0005t0001g0041 | 2 | HG03195.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1596+193A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767663 | ||||||
chr16:767663
|
A | T | 2 | a0001c0001t0001g0148a0008c0009t0002g0257 | 2 | HG03209.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1596+193A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767663 | ||||||
chr16:767664
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1596+194G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767664 | ||||||
chr16:767664
|
GC | G | 4 | a0002c0002t0002g0055a0003c0004t0003g0227a0003c0004t0003g0273others(1): Show | 4 | HG02486.hp2 HG02818.hp2 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+195delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767664 | ||||||
chr16:767665
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+195C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767665 | ||||||
chr16:767665
|
C | T | 19 | a0001c0001t0001g0042a0001c0001t0001g0081a0001c0001t0001g0087others(16): Show | 20 | HG00099.hp1 HG02040.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596+195C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767665 | ||||||
chr16:767666
|
G | A | 14 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0160others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+196G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767666 | ||||||
chr16:767666
|
GTGGGGGG others(3): Show |
G | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+197_1596+206d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767666 | ||||||
chr16:767667
|
T | A | 5 | a0001c0001t0001g0067a0002c0002t0002g0055a0003c0004t0003g0227others(2): Show | 5 | HG02486.hp2 HG02818.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+197T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767667 | ||||||
chr16:767667
|
T | G | 2 | a0001c0001t0001g0244a0004c0006t0001g0350 | 2 | HG03195.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1596+197T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767667 | ||||||
chr16:767667
|
T | TG | 30 | a0001c0001t0001g0042a0001c0001t0001g0081a0001c0001t0001g0091others(27): Show | 34 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596+203dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | |||||
chr16:767667
|
T | TGGAG | 9 | a0001c0022t0001g0270a0006c0010t0001g0013a0006c0010t0001g0237others(6): Show | 14 | HG01361.hp1 HG01981.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | |||||
chr16:767667
|
T | TGGAGG | 28 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0223others(25): Show | 32 | HG00733.hp2 HG00738.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | |||||
chr16:767667
|
T | TGGAGGAG others(40): Show |
1 | a0001c0001t0001g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+199_1596+200i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | |||||
chr16:767668
|
G | GGA | 11 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(8): Show | 11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767668 | |||||
chr16:767668
|
GGGGGGCG others(57): Show |
G | 1 | a0001c0001t0001g0166 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1596+199_1596+262d others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767668 | ||||||
chr16:767668
|
GGGGGGCG others(111): Show |
G | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1596+204_1596+321d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767668 | |||||
chr16:767669
|
G | GAGGA | 13 | a0004c0006t0001g0240a0004c0006t0001g0262a0008c0009t0002g0028others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767669 | ||||||
chr16:767670
|
G | A | 5 | a0001c0001t0001g0172a0001c0001t0001g0205a0002c0002t0002g0322others(2): Show | 5 | HG01346.hp2 HG02056.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+200G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767670 | ||||||
chr16:767671
|
G | A | 11 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(8): Show | 11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+201G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767671 | ||||||
chr16:767672
|
G | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0073others(38): Show | 45 | HG00733.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1596+202G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767672 | ||||||
chr16:767672
|
G | GCGCGTGG others(75): Show |
1 | a0001c0001t0001g0106 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1596+202_1596+203i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767672 | ||||||
chr16:767672
|
G | GGCGGCGT others(50): Show |
1 | a0001c0001t0001g0199 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1596+205_1596+206i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGCGTGGA others(8): Show |
3 | a0005c0005t0001g0027a0005c0005t0001g0031a0029c0046t0001g0034 | 3 | HG00609.hp2 HG00738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1596+212_1596+226d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGCGTGGA others(64): Show |
1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1596+230_1596+231i others(73): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGCGTGA others(57): Show |
1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGCGTGG others(248): Show |
1 | a0001c0001t0001g0292 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(257): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGCGTGG others(8): Show |
1 | a0005c0005t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGCGTGG others(91): Show |
3 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0162 | 3 | HG00609.hp1 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGGCGCA others(21): Show |
1 | a0001c0001t0001g0286 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGGGC | 47 | a0001c0001t0001g0241a0002c0002t0002g0001a0002c0002t0002g0017others(44): Show | 58 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1596+203_1596+204i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGTGTGG others(34): Show |
3 | a0004c0006t0001g0224a0004c0006t0001g0346a0004c0021t0001g0298 | 3 | HG00558.hp1 HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGTGTGG others(314): Show |
1 | a0016c0028t0001g0187 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(323): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGTGTGG others(58): Show |
1 | a0001c0001t0001g0163 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1596+203_1596+204i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGTGTGG others(87): Show |
2 | a0001c0001t0001g0119a0001c0001t0010g0140 | 2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(96): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGTGTGG others(63): Show |
1 | a0001c0001t0001g0105 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1596+203_1596+204i others(72): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | GGGTGTGG others(219): Show |
1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1596+203_1596+204i others(228): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | |||||
chr16:767672
|
G | T | 15 | a0001c0001t0001g0148a0002c0002t0002g0295a0002c0003t0002g0253others(12): Show | 20 | HG01981.hp1 HG02055.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596+202G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767672 | ||||||
chr16:767674
|
C | A | 11 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(8): Show | 11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+204C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767674 | ||||||
chr16:767674
|
C | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(4): Show | 7 | HG00558.hp2 HG03492.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+204C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767674 | ||||||
chr16:767674
|
C | T | 20 | a0001c0001t0001g0107a0001c0001t0001g0157a0001c0001t0001g0180others(17): Show | 24 | HG00639.hp1 HG00642.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1596+204C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767674 | ||||||
chr16:767676
|
T | A | 3 | a0003c0004t0003g0269a0004c0006t0001g0240a0004c0006t0001g0262 | 3 | HG00423.hp2 HG04204.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1596+206T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767676 | ||||||
chr16:767676
|
T | C | 18 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(15): Show | 18 | HG00558.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+206T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767676 | ||||||
chr16:767676
|
T | G | 12 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(9): Show | 12 | HG01884.hp1 HG02071.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+206T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767676 | ||||||
chr16:767678
|
G | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(4): Show | 7 | HG00558.hp2 HG03492.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+208G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767678 | ||||||
chr16:767678
|
G | T | 10 | a0001c0001t0001g0147a0008c0009t0002g0028a0008c0009t0002g0044others(7): Show | 10 | HG01891.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+208G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767678 | ||||||
chr16:767679
|
A | AGGGGGGC others(14): Show |
1 | a0002c0002t0002g0307 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1596+211_1596+212i others(23): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767679 | |||||
chr16:767679
|
A | C | 11 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(8): Show | 11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+209A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767679 | ||||||
chr16:767679
|
A | G | 11 | a0001c0001t0001g0147a0008c0009t0002g0028a0008c0009t0002g0044others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+209A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767679 | ||||||
chr16:767680
|
G | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(4): Show | 7 | HG00558.hp2 HG03492.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+210G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767680 | ||||||
chr16:767680
|
GGAGGGGC others(18): Show |
G | 2 | a0001c0001t0001g0136a0001c0001t0001g0195 | 2 | HG00544.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1596+212_1596+236d others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767680 | |||||
chr16:767681
|
G | C | 11 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(8): Show | 11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+211G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767681 | ||||||
chr16:767681
|
GA | G | 79 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(76): Show | 94 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.1596+212delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767681 | ||||||
chr16:767682
|
A | AGGGGCGC others(6): Show |
2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1596+223_1596+224i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767682 | |||||
chr16:767682
|
A | ATG | 11 | a0001c0022t0001g0178a0004c0006t0001g0181a0004c0006t0001g0185others(8): Show | 11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+212_1596+213i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767682 | ||||||
chr16:767682
|
A | G | 17 | a0001c0001t0001g0147a0002c0002t0002g0193a0002c0002t0002g0294others(14): Show | 17 | HG01891.hp2 HG02015.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+212A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767682 | ||||||
chr16:767687
|
C | G | 18 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(15): Show | 18 | HG00558.hp2 HG02071.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+217C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767687 | ||||||
chr16:767687
|
C | T | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+217C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767687 | ||||||
chr16:767688
|
G | A | 1 | a0017c0023t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1596+218G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767688 | ||||||
chr16:767689
|
C | CATGGGGG others(4): Show |
1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1596+219_1596+220i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767689 | ||||||
chr16:767689
|
C | CATGGGGG others(3): Show |
1 | a0004c0006t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1596+219_1596+220i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767689 | ||||||
chr16:767689
|
C | CGTGGGGG others(3): Show |
1 | a0002c0003t0004g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+223_1596+224i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767689 | |||||
chr16:767689
|
C | T | 13 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0022t0001g0178others(10): Show | 13 | HG00099.hp1 HG02071.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+219C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767689 | ||||||
chr16:767690
|
G | A | 2 | a0001c0001t0001g0147a0003c0004t0003g0269 | 2 | HG00423.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1596+220G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767690 | ||||||
chr16:767691
|
TGGAGGGG others(20): Show |
T | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+227_1596+253d others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767691 | |||||
chr16:767692
|
G | GGGAGGAG others(8): Show |
1 | a0001c0001t0001g0176 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1596+223_1596+224i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767692 | |||||
chr16:767692
|
GGA | G | 9 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(6): Show | 13 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+224_1596+225d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767692 | |||||
chr16:767694
|
A | G | 7 | a0001c0001t0001g0147a0002c0002t0002g0295a0002c0003t0002g0253others(4): Show | 7 | HG00423.hp2 HG02155.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+224A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767694 | ||||||
chr16:767694
|
AGGGGGGA others(4): Show |
A | 6 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(3): Show | 6 | HG02523.hp2 HG03579.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+231_1596+241d others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767694 | |||||
chr16:767694
|
AGGGGGGA others(42): Show |
A | 1 | a0007c0016t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+227_1596+275d others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767694 | |||||
chr16:767695
|
G | GGAGGAGG others(7): Show |
1 | a0002c0003t0004g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1596+226_1596+227i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767695 | |||||
chr16:767695
|
G | GGAGGAGG others(112): Show |
1 | a0002c0003t0004g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1596+226_1596+227i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767695 | |||||
chr16:767695
|
GGGGGGAG others(3): Show |
G | 1 | a0001c0001t0001g0355 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1596+231_1596+240d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767695 | |||||
chr16:767696
|
G | GA | 67 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0112others(64): Show | 79 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1596+226_1596+227i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767696 | ||||||
chr16:767696
|
G | T | 7 | a0001c0001t0001g0223a0006c0007t0001g0008a0006c0007t0001g0014others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+226G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767696 | ||||||
chr16:767696
|
GGGGGAGT others(30): Show |
G | 1 | a0015c0020t0002g0297 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1596+231_1596+267d others(39): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767696 | |||||
chr16:767697
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+227G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767697 | ||||||
chr16:767697
|
G | T | 1 | a0003c0004t0003g0277 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1596+227G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767697 | ||||||
chr16:767699
|
G | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0241a0003c0004t0003g0277 | 3 | HG02717.hp1 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1596+229G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | ||||||
chr16:767699
|
G | GC | 21 | a0001c0001t0001g0172a0001c0001t0001g0252a0002c0002t0002g0007others(18): Show | 23 | HG00738.hp1 HG01109.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+229_1596+230i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | ||||||
chr16:767699
|
G | GCACGTGG others(22): Show |
1 | a0002c0002t0002g0310 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1596+229_1596+230i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | ||||||
chr16:767699
|
G | GT | 6 | a0002c0003t0004g0211a0002c0003t0004g0230a0002c0003t0004g0231others(3): Show | 6 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+229_1596+230i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | ||||||
chr16:767699
|
G | T | 10 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(7): Show | 14 | HG00423.hp2 HG00639.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+229G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | ||||||
chr16:767700
|
G | C | 113 | a0000c0039t0008g0146a0001c0001t0001g0010a0001c0001t0001g0011others(110): Show | 116 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1596+230G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767700 | ||||||
chr16:767700
|
G | GCGCGTGG others(928): Show |
1 | a0001c0001t0001g0075 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1596+230_1596+231i others(937): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767700 | ||||||
chr16:767701
|
A | ACGTG | 7 | a0001c0001t0001g0223a0006c0007t0001g0008a0006c0007t0001g0014others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+231_1596+232i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | ||||||
chr16:767701
|
A | C | 280 | a0000c0039t0008g0146a0001c0001t0001g0005a0001c0001t0001g0010others(277): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1596+231A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | ||||||
chr16:767701
|
A | G | 3 | a0001c0001t0001g0172a0002c0003t0004g0212a0002c0003t0004g0216 | 3 | HG01952.hp2 HG01978.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1596+231A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | ||||||
chr16:767701
|
A | T | 11 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(8): Show | 11 | HG00423.hp2 HG00558.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+231A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | ||||||
chr16:767703
|
T | A | 7 | a0001c0001t0001g0223a0006c0007t0001g0008a0006c0007t0001g0014others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+233T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767703 | ||||||
chr16:767703
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0073others(154): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1596+233T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767703 | ||||||
chr16:767703
|
T | G | 3 | a0001c0001t0001g0147a0003c0004t0003g0269a0003c0004t0003g0277 | 3 | HG00423.hp2 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1596+233T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767703 | ||||||
chr16:767703
|
T | TG | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0002c0002t0002g0310others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+234dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767703 | |||||
chr16:767703
|
T | TGGA | 26 | a0001c0001t0001g0241a0001c0001t0001g0252a0002c0002t0002g0007others(23): Show | 28 | HG00738.hp1 HG01109.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1596+234_1596+235i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767703 | |||||
chr16:767704
|
G | A | 6 | a0001c0001t0001g0147a0001c0001t0001g0158a0001c0022t0001g0270others(3): Show | 6 | HG00423.hp2 HG01361.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+234G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767704 | ||||||
chr16:767704
|
G | GGAGGAGC others(111): Show |
1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+234_1596+235i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767704 | ||||||
chr16:767705
|
T | A | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0002c0002t0002g0310others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+235T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767705 | ||||||
chr16:767705
|
T | G | 49 | a0001c0001t0001g0147a0001c0001t0001g0223a0001c0001t0001g0241others(46): Show | 56 | HG00423.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1596+235T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767705 | ||||||
chr16:767705
|
T | TGGA | 62 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0134others(59): Show | 78 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1596+237_1596+238i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | |||||
chr16:767705
|
T | TGGAGGGG others(21): Show |
7 | a0001c0001t0001g0112a0001c0001t0001g0121a0001c0001t0001g0151others(4): Show | 7 | HG00639.hp2 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+237_1596+238i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | |||||
chr16:767705
|
T | TGGAGGGG others(317): Show |
1 | a0005c0005t0001g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(326): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | |||||
chr16:767705
|
T | TGGAGGGG others(127): Show |
1 | a0005c0005t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(136): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | |||||
chr16:767705
|
TG | T | 13 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0090others(10): Show | 13 | HG00280.hp2 HG00642.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+242delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | |||||
chr16:767706
|
G | A | 48 | a0001c0001t0001g0071a0001c0001t0001g0154a0001c0001t0001g0223others(45): Show | 55 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1596+236G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767706 | ||||||
chr16:767706
|
G | C | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+236G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767706 | ||||||
chr16:767706
|
G | GGAGGA | 23 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0131others(20): Show | 23 | HG00558.hp2 HG01934.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+237_1596+238i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | |||||
chr16:767706
|
G | GGAGGAGG others(26): Show |
1 | a0006c0007t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(35): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | |||||
chr16:767706
|
G | GGAGGGGG others(75): Show |
1 | a0005c0005t0001g0037 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | |||||
chr16:767706
|
G | GGGGGGGC others(162): Show |
1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | |||||
chr16:767706
|
G | GGGGGGGC others(45): Show |
1 | a0001c0001t0001g0200 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | |||||
chr16:767708
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0134others(9): Show | 17 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596+238G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767708 | ||||||
chr16:767710
|
G | T | 1 | a0004c0006t0001g0350 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1596+240G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767710 | ||||||
chr16:767711
|
G | C | 138 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0112others(135): Show | 152 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.1596+241G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | ||||||
chr16:767711
|
G | GCGTGGAG others(167): Show |
1 | a0005c0005t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+241_1596+242i others(176): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | ||||||
chr16:767711
|
G | GCGTGGAG others(456): Show |
1 | a0024c0040t0001g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1596+241_1596+242i others(465): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | ||||||
chr16:767711
|
G | GCGTGGAG others(6): Show |
1 | a0001c0001t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596+241_1596+242i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | ||||||
chr16:767711
|
G | GGAGTGTG others(515): Show |
1 | a0001c0001t0001g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(524): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGCGTG others(33): Show |
2 | a0002c0003t0004g0218a0002c0003t0004g0219 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1596+244_1596+245i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGGTGG others(8): Show |
1 | a0001c0001t0001g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+244_1596+245i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(8): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0108 | 2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(46): Show |
1 | a0001c0001t0001g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(99): Show |
1 | a0009c0011t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(553): Show |
1 | a0001c0008t0001g0305 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(562): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(552): Show |
1 | a0001c0008t0001g0306 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(561): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(366): Show |
1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(375): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(74): Show |
2 | a0004c0017t0001g0142a0004c0017t0001g0263 | 2 | HG03834.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(83): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(784): Show |
1 | a0001c0001t0001g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(793): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(688): Show |
1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(697): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(405): Show |
1 | a0001c0001t0001g0281 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(414): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(351): Show |
1 | a0001c0001t0001g0096 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(360): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(432): Show |
1 | a0001c0001t0001g0280 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(441): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(373): Show |
1 | a0001c0001t0001g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(382): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(7): Show |
61 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0056others(58): Show | 63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1596+250_1596+251i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(498): Show |
1 | a0001c0001t0001g0351 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(507): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(155): Show |
1 | a0000c0039t0008g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(164): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(49): Show |
1 | a0001c0001t0001g0137 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(102): Show |
1 | a0001c0038t0001g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(111): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(179): Show |
1 | a0001c0001t0001g0104 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(188): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGCGTGGA others(8): Show |
1 | a0011c0014t0001g0145 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(33): Show |
1 | a0001c0008t0001g0303 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(20): Show |
1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(156): Show |
1 | a0001c0001t0001g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(20): Show |
1 | a0001c0001t0001g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(35): Show |
1 | a0001c0001t0001g0130 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(44): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(156): Show |
1 | a0001c0001t0001g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(238): Show |
1 | a0001c0001t0001g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(247): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(156): Show |
1 | a0026c0030t0001g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(34): Show |
1 | a0001c0035t0001g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(36): Show |
2 | a0001c0001t0001g0110a0012c0018t0001g0078 | 2 | HG01256.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1596+242_1596+243i others(45): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGCAT others(73): Show |
1 | a0001c0001t0001g0077 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(82): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGTGG others(8): Show |
2 | a0001c0001t0001g0093a0027c0026t0001g0169 | 2 | HG01175.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1596+242_1596+243i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGGCGTGG others(11): Show |
1 | a0025c0042t0001g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(20): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGCGTG others(498): Show |
1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(507): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(21): Show |
1 | a0001c0022t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(125): Show |
1 | a0001c0001t0011g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(245): Show |
1 | a0001c0001t0001g0132 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(254): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(163): Show |
1 | a0002c0003t0001g0059 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(161): Show |
1 | a0001c0001t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(170): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(313): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(322): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | GGTGTGGA others(763): Show |
1 | a0001c0001t0001g0158 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(772): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767711
|
G | T | 7 | a0001c0001t0001g0147a0002c0002t0002g0235a0002c0002t0002g0308others(4): Show | 7 | HG02300.hp2 HG02523.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+241G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | ||||||
chr16:767711
|
GGCGTGGA others(139): Show |
G | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1596+254_1596+399d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | |||||
chr16:767712
|
G | GCGTGGAG others(7): Show |
1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767712 | |||||
chr16:767713
|
C | A | 1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+243C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767713 | ||||||
chr16:767713
|
C | G | 3 | a0002c0002t0002g0295a0002c0003t0002g0253a0003c0004t0003g0226 | 3 | HG03225.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+243C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767713 | ||||||
chr16:767713
|
C | T | 13 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0106others(10): Show | 13 | HG00558.hp1 HG02083.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+243C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767713 | ||||||
chr16:767714
|
GT | G | 15 | a0001c0001t0001g0134a0002c0003t0004g0215a0002c0015t0003g0066others(12): Show | 23 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+245delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767714 | ||||||
chr16:767715
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0073a0008c0009t0002g0044others(2): Show | 6 | HG01109.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+245T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767715 | ||||||
chr16:767715
|
T | C | 3 | a0002c0002t0002g0295a0002c0003t0002g0253a0003c0004t0003g0226 | 3 | HG03225.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+245T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767715 | ||||||
chr16:767715
|
TGGA | T | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0002c0002t0002g0235others(4): Show | 7 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+254_1596+256d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767715 | |||||
chr16:767716
|
G | C | 15 | a0001c0001t0001g0134a0002c0003t0004g0215a0002c0015t0003g0066others(12): Show | 23 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+246G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767716 | ||||||
chr16:767716
|
G | GC | 3 | a0002c0002t0002g0295a0002c0003t0002g0253a0003c0004t0003g0226 | 3 | HG03225.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+246_1596+247i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767716 | ||||||
chr16:767717
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+247G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767717 | ||||||
chr16:767718
|
A | AGGAGGGG others(5): Show |
2 | a0005c0005t0001g0031a0009c0011t0001g0340 | 2 | HG00738.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | AGGGGGGC others(4): Show |
3 | a0001c0001t0001g0120a0001c0001t0001g0157a0029c0046t0001g0034 | 3 | HG00609.hp2 HG02145.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1596+250_1596+251i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | AGGGGGGC others(61): Show |
1 | a0001c0008t0001g0300 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | AGGGGGGC others(216): Show |
2 | a0004c0006t0001g0224a0004c0021t0001g0298 | 2 | HG00558.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1596+250_1596+251i others(225): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | AGGGGGGC others(217): Show |
1 | a0004c0006t0001g0346 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(226): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | AGGGGGGC others(27): Show |
1 | a0001c0001t0001g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(36): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | AGGGGGGC others(53): Show |
1 | a0001c0041t0001g0152 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(62): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | |||||
chr16:767718
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+248A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767718 | ||||||
chr16:767718
|
A | T | 19 | a0001c0001t0001g0134a0002c0002t0002g0295a0002c0003t0002g0253others(16): Show | 27 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1596+248A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767718 | ||||||
chr16:767719
|
G | GGGGGGCG others(149): Show |
1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(158): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767719 | |||||
chr16:767720
|
G | GGGGGCGC others(220): Show |
1 | a0001c0001t0001g0138 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(229): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767720 | ||||||
chr16:767720
|
G | GGGGGCGC others(69): Show |
1 | a0001c0001t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767720 | ||||||
chr16:767720
|
GAGGA | G | 5 | a0001c0001t0001g0106a0001c0001t0001g0179a0003c0004t0003g0227others(2): Show | 5 | HG02486.hp2 HG02818.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+251_1596+254d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767720 | ||||||
chr16:767721
|
A | AGGGGCGC others(2): Show |
10 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0105others(7): Show | 10 | HG00280.hp2 HG00642.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+253_1596+254i others(11): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | AGGGGCGC others(100): Show |
1 | a0005c0005t0001g0027 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(109): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | AGGGGCGC others(85): Show |
1 | a0001c0001t0001g0341 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(94): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | AGGGGCGC others(102): Show |
1 | a0001c0001t0001g0143 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(111): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | AGGGGCGC others(17): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0286 | 2 | HG01361.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | AGGGGCGC others(236): Show |
1 | a0001c0001t0001g0201 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(245): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | AGGGGCGC others(33): Show |
1 | a0017c0023t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | |||||
chr16:767721
|
A | G | 8 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0126others(5): Show | 8 | HG01952.hp2 HG02683.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+251A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767721 | ||||||
chr16:767721
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+251A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767721 | ||||||
chr16:767722
|
G | GGGCGCGT others(3): Show |
1 | a0001c0001t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767722 | |||||
chr16:767722
|
G | GGGGCGCG others(4): Show |
10 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0115others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+253_1596+254i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767722 | |||||
chr16:767722
|
G | GGGGCGCG others(18): Show |
2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767722 | |||||
chr16:767724
|
A | G | 38 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0091others(35): Show | 42 | HG00609.hp1 HG00639.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1596+254A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767724 | ||||||
chr16:767725
|
G | C | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+255G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767725 | ||||||
chr16:767727
|
G | C | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+257G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767727 | ||||||
chr16:767728
|
G | GGC | 14 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0105others(11): Show | 14 | HG00280.hp2 HG00597.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+258_1596+259i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767728 | ||||||
chr16:767729
|
C | A | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1596+259C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767729 | ||||||
chr16:767729
|
C | T | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+259C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767729 | ||||||
chr16:767730
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+260G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767730 | ||||||
chr16:767731
|
C | A | 4 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246others(1): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+261C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | ||||||
chr16:767731
|
C | CGTGGAGG others(60): Show |
1 | a0029c0046t0001g0034 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1596+261_1596+262i others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | ||||||
chr16:767731
|
C | CGTGGAGG others(106): Show |
1 | a0001c0001t0001g0120 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1596+261_1596+262i others(115): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | ||||||
chr16:767731
|
C | G | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+261C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | ||||||
chr16:767731
|
C | T | 29 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0086others(26): Show | 33 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1596+261C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | ||||||
chr16:767731
|
CATGGGGG others(3): Show |
C | 2 | a0002c0002t0002g0295a0002c0003t0002g0253 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+262_1596+271d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | ||||||
chr16:767732
|
A | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0081others(70): Show | 82 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1596+262A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767732 | ||||||
chr16:767733
|
T | C | 4 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246others(1): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+263T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767733 | ||||||
chr16:767733
|
T | G | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+263T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767733 | ||||||
chr16:767733
|
T | TGGAGGGG others(85): Show |
1 | a0001c0001t0001g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1596+265_1596+266i others(94): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767733 | |||||
chr16:767734
|
G | GGAGGGGG others(6): Show |
1 | a0005c0005t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596+265_1596+266i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767734 | |||||
chr16:767736
|
G | A | 1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+266G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767736 | ||||||
chr16:767737
|
G | A | 4 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246others(1): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+267G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767737 | ||||||
chr16:767739
|
G | C | 6 | a0001c0041t0001g0152a0004c0006t0001g0224a0004c0006t0001g0346others(3): Show | 6 | HG00558.hp1 HG02155.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+269G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767739 | ||||||
chr16:767739
|
G | T | 6 | a0001c0001t0001g0106a0001c0001t0001g0179a0001c0001t0001g0205others(3): Show | 6 | HG02056.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+269G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767739 | ||||||
chr16:767741
|
T | C | 45 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(42): Show | 45 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1596+271T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767741 | ||||||
chr16:767741
|
T | G | 2 | a0002c0003t0004g0214a0002c0003t0004g0215 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+271T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767741 | ||||||
chr16:767741
|
T | TGC | 11 | a0001c0001t0001g0087a0001c0001t0001g0166a0001c0001t0001g0244others(8): Show | 15 | HG00639.hp1 HG01070.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596+272_1596+273i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | |||||
chr16:767741
|
T | TGTGGAGG others(71): Show |
1 | a0001c0001t0001g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1596+283_1596+284i others(80): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | |||||
chr16:767741
|
T | TGTGGAGG others(60): Show |
1 | a0005c0005t0001g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1596+290_1596+356d others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | |||||
chr16:767741
|
T | TGTGGAGG others(99): Show |
2 | a0001c0001t0001g0109a0001c0035t0001g0206 | 2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1596+345_1596+346i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | |||||
chr16:767742
|
G | C | 2 | a0002c0003t0004g0214a0002c0003t0004g0215 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+272G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767742 | ||||||
chr16:767743
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+273T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767743 | ||||||
chr16:767743
|
T | C | 2 | a0002c0003t0004g0214a0002c0003t0004g0215 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+273T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767743 | ||||||
chr16:767745
|
G | C | 1 | a0002c0003t0004g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+275G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767745 | ||||||
chr16:767746
|
A | AGGGGGGC others(122): Show |
1 | a0008c0009t0002g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767746 | |||||
chr16:767746
|
A | AGGGGGGC others(135): Show |
1 | a0001c0001t0001g0094 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(144): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767746 | |||||
chr16:767746
|
A | AGGGGGGT others(58): Show |
2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+282_1596+283i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767746 | |||||
chr16:767746
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0179a0001c0001t0001g0205others(1): Show | 4 | HG02056.hp1 HG02300.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+276A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767746 | ||||||
chr16:767746
|
A | T | 1 | a0002c0003t0004g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1596+276A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767746 | ||||||
chr16:767747
|
G | GGGGGGCG others(329): Show |
1 | a0004c0006t0001g0267 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(338): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767747 | |||||
chr16:767747
|
G | T | 1 | a0002c0003t0004g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+277G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767747 | ||||||
chr16:767748
|
G | A | 4 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246others(1): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+278G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767748 | ||||||
chr16:767748
|
G | GA | 21 | a0001c0001t0001g0087a0001c0001t0001g0166a0001c0001t0001g0244others(18): Show | 25 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+278_1596+279i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767748 | ||||||
chr16:767748
|
G | GGGGCACG others(48): Show |
2 | a0001c0001t0001g0106a0001c0001t0001g0205 | 2 | HG02056.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1596+281_1596+282i others(57): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCAC others(49): Show |
1 | a0001c0001t0001g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1596+283_1596+284i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(125): Show |
1 | a0005c0005t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596+295_1596+296i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(289): Show |
1 | a0001c0001t0001g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1596+299_1596+300i others(298): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(165): Show |
1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(174): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(162): Show |
1 | a0009c0011t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(189): Show |
1 | a0001c0001t0001g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(198): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(361): Show |
1 | a0004c0017t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(370): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(136): Show |
1 | a0001c0001t0001g0132 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(145): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(190): Show |
1 | a0001c0008t0001g0303 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(199): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(136): Show |
3 | a0008c0009t0002g0044a0008c0009t0002g0045a0008c0009t0002g0048 | 3 | HG01891.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(145): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(137): Show |
1 | a0008c0009t0002g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(146): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(137): Show |
2 | a0006c0007t0001g0014a0006c0007t0001g0258 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(146): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(136): Show |
1 | a0001c0001t0001g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(145): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(400): Show |
1 | a0005c0005t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(409): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(162): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(198): Show |
1 | a0001c0001t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(207): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(57): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0133 | 2 | HG00597.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1596+289_1596+290i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGCGC others(72): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0172 | 2 | NA18979.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1596+289_1596+290i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | GGGGGTGC others(8): Show |
1 | a0001c0001t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+282_1596+283i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767748
|
G | T | 1 | a0017c0023t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+278G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767748 | ||||||
chr16:767748
|
GGGGGCGC others(8): Show |
G | 5 | a0001c0001t0001g0060a0002c0002t0002g0294a0002c0002t0002g0325others(2): Show | 5 | HG02074.hp2 HG02080.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+293_1596+307d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | |||||
chr16:767749
|
G | GGGGCGCG others(50): Show |
1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767749 | |||||
chr16:767751
|
G | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0073a0007c0016t0001g0043others(1): Show | 5 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+281G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767751 | ||||||
chr16:767752
|
G | GCGCGTGG others(19): Show |
1 | a0002c0003t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1596+295_1596+296i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767752
|
G | GCGCGTGG others(19): Show |
33 | a0000c0039t0008g0146a0001c0001t0001g0110a0001c0001t0001g0116others(30): Show | 33 | HG00558.hp2 HG00738.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767752
|
G | GCGCGTGG others(115): Show |
4 | a0002c0002t0002g0188a0002c0002t0002g0321a0002c0002t0002g0323others(1): Show | 4 | HG00733.hp2 NA18940.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767752
|
G | GCGCGTGG others(274): Show |
1 | a0002c0002t0002g0324 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(283): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767752
|
G | GCGCGTGG others(159): Show |
1 | a0002c0003t0004g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(168): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767752
|
G | GCGCGTGG others(20): Show |
1 | a0001c0001t0001g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767752
|
G | GCGCGTGG others(6): Show |
1 | a0005c0045t0001g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | |||||
chr16:767753
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0073a0007c0016t0001g0043others(1): Show | 5 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+283C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767753 | ||||||
chr16:767753
|
C | CGCGTGGA others(96): Show |
1 | a0001c0001t0001g0241 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1596+307_1596+308i others(105): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGA others(132): Show |
1 | a0001c0001t0001g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(141): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGA others(121): Show |
1 | a0002c0003t0001g0059 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGA others(121): Show |
1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGA others(43): Show |
1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGA others(108): Show |
1 | a0004c0017t0001g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(117): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGG others(390): Show |
1 | a0001c0001t0001g0339 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGG others(42): Show |
1 | a0005c0005t0001g0033 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1596+289_1596+290i others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGG others(219): Show |
1 | a0001c0001t0001g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(228): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | CGCGTGGG others(230): Show |
1 | a0009c0011t0001g0340 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1596+289_1596+290i others(239): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | |||||
chr16:767753
|
C | G | 2 | a0002c0003t0004g0214a0002c0003t0004g0215 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+283C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767753 | ||||||
chr16:767753
|
C | T | 6 | a0001c0001t0001g0122a0001c0001t0001g0138a0001c0001t0001g0222others(3): Show | 6 | HG01099.hp1 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+283C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767753 | ||||||
chr16:767754
|
G | A | 4 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246others(1): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+284G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767754 | ||||||
chr16:767754
|
G | GCGTGGAG others(6): Show |
3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0108 | 3 | NA18952.hp1 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767754 | |||||
chr16:767755
|
C | A | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+285C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767755 | ||||||
chr16:767755
|
C | CGTGGAGG others(18): Show |
1 | a0002c0003t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1596+287_1596+311d others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767755 | |||||
chr16:767755
|
C | CGTGGAGG others(75): Show |
1 | a0002c0003t0002g0268 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767755 | |||||
chr16:767755
|
C | CGTGGAGG others(19): Show |
1 | a0004c0021t0001g0345 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767755 | |||||
chr16:767756
|
G | A | 1 | a0002c0003t0004g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1596+286G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767756 | ||||||
chr16:767756
|
G | GTGGAGGG others(63): Show |
1 | a0001c0001t0001g0285 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(72): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767756 | |||||
chr16:767756
|
GT | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0073a0007c0016t0001g0043others(1): Show | 5 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+287delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767756 | ||||||
chr16:767757
|
T | TGGA | 3 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304 | 3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+293_1596+295d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767757 | |||||
chr16:767757
|
TGGAGGAG others(50): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1596+290_1596+346d others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767757 | |||||
chr16:767760
|
A | AGGGGGCA others(3): Show |
5 | a0002c0002t0002g0049a0002c0002t0002g0314a0002c0002t0002g0336others(2): Show | 5 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | |||||
chr16:767760
|
A | AGGGGGCA others(176): Show |
1 | a0002c0002t0002g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(185): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | |||||
chr16:767760
|
A | AGGGGGCA others(81): Show |
1 | a0008c0009t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(90): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | |||||
chr16:767760
|
A | AGGGGGGC others(40): Show |
1 | a0014c0024t0002g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | |||||
chr16:767760
|
A | G | 3 | a0001c0001t0001g0160a0003c0004t0003g0226a0005c0005t0001g0025 | 3 | HG02886.hp2 NA19089.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+290A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767760 | ||||||
chr16:767760
|
A | T | 2 | a0002c0003t0004g0212a0004c0006t0001g0350 | 2 | HG01978.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1596+290A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767760 | ||||||
chr16:767761
|
G | GGGGGCAC others(99): Show |
1 | a0002c0002t0002g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | |||||
chr16:767761
|
G | GGGGGCAC others(74): Show |
24 | a0002c0002t0002g0001a0002c0002t0002g0017a0002c0002t0002g0055others(21): Show | 32 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(83): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | |||||
chr16:767761
|
G | GGGGGCAC others(88): Show |
1 | a0002c0002t0002g0330 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(97): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | |||||
chr16:767761
|
G | GGGGGCAC others(44): Show |
3 | a0002c0002t0002g0018a0002c0002t0002g0326a0002c0002t0002g0327 | 4 | HG01069.hp1 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(53): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | |||||
chr16:767761
|
GGA | G | 24 | a0001c0001t0001g0071a0001c0001t0001g0223a0001c0022t0001g0270others(21): Show | 27 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1596+293_1596+294d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | |||||
chr16:767762
|
G | GGGGCACG others(60): Show |
1 | a0002c0002t0002g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | ||||||
chr16:767762
|
G | GGGGCACG others(156): Show |
1 | a0002c0002t0002g0316 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | ||||||
chr16:767762
|
G | GGGGCGCG others(4): Show |
4 | a0002c0003t0004g0218a0002c0003t0004g0219a0002c0015t0003g0255others(1): Show | 4 | HG02109.hp1 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | ||||||
chr16:767762
|
GA | G | 3 | a0002c0002t0002g0007a0002c0002t0002g0328a0003c0004t0003g0276 | 5 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+293delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | ||||||
chr16:767763
|
A | AGGAGGGG others(20): Show |
3 | a0001c0001t0001g0056a0001c0001t0001g0134a0001c0001t0001g0163 | 3 | HG01169.hp1 HG03490.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1596+295_1596+296i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | |||||
chr16:767763
|
A | AGGCACGT others(79): Show |
1 | a0002c0003t0004g0217 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1596+295_1596+296i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | |||||
chr16:767763
|
A | AGGGGCGC others(7): Show |
1 | a0001c0001t0001g0122 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1596+298_1596+311d others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | |||||
chr16:767763
|
A | AGGGGCGC others(409): Show |
1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+307_1596+308i others(418): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | |||||
chr16:767763
|
A | AGGGGCGC others(8): Show |
1 | a0005c0005t0009g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596+297_1596+311d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | |||||
chr16:767763
|
A | G | 50 | a0001c0001t0001g0160a0001c0001t0001g0348a0001c0001t0001g0349others(47): Show | 59 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1596+293A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767763 | ||||||
chr16:767763
|
AGGGGCGC others(58): Show |
A | 1 | a0012c0018t0001g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1596+301_1596+365d others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | |||||
chr16:767767
|
G | GT | 5 | a0002c0002t0002g0049a0002c0002t0002g0314a0002c0002t0002g0336others(2): Show | 5 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+297_1596+298i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767767 | ||||||
chr16:767768
|
C | CGCGTGGA others(21): Show |
1 | a0002c0003t0001g0059 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+307_1596+308i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767768 | |||||
chr16:767768
|
C | G | 3 | a0002c0002t0002g0289a0002c0002t0002g0316a0028c0044t0002g0250 | 3 | HG04199.hp1 NA19030.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1596+298C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767768 | ||||||
chr16:767768
|
C | T | 1 | a0004c0006t0001g0224 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1596+298C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767768 | ||||||
chr16:767769
|
G | A | 20 | a0001c0001t0001g0071a0001c0001t0001g0160a0001c0001t0001g0223others(17): Show | 21 | HG01361.hp1 HG01981.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1596+299G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767769 | ||||||
chr16:767769
|
GCGTGGA | G | 1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+300_1596+305d others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767769 | ||||||
chr16:767770
|
C | A | 4 | a0002c0003t0004g0234a0007c0012t0001g0004a0007c0012t0001g0245others(1): Show | 6 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+300C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767770 | ||||||
chr16:767770
|
C | T | 6 | a0002c0002t0002g0289a0002c0002t0002g0316a0003c0004t0003g0227others(3): Show | 6 | HG02486.hp2 HG02818.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+300C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767770 | ||||||
chr16:767771
|
G | A | 3 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304 | 3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+301G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767771 | ||||||
chr16:767771
|
G | GC | 3 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+301_1596+302i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767771 | ||||||
chr16:767772
|
T | G | 3 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+302T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767772 | ||||||
chr16:767775
|
A | G | 5 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304others(2): Show | 5 | HG02027.hp1 HG02818.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+305A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767775 | ||||||
chr16:767775
|
AG | A | 8 | a0001c0001t0001g0075a0001c0001t0001g0149a0002c0002t0002g0235others(5): Show | 8 | HG00408.hp1 HG00733.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+311delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767775 | |||||
chr16:767775
|
AGGGGGGA others(69): Show |
A | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1596+311_1596+386d others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767775 | |||||
chr16:767776
|
G | A | 3 | a0002c0003t0004g0214a0002c0003t0004g0215a0013c0019t0001g0006 | 5 | HG02293.hp2 HG02300.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+306G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767776 | ||||||
chr16:767776
|
GGGGGGAG others(3): Show |
G | 15 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0223others(12): Show | 17 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596+312_1596+321d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767776 | |||||
chr16:767777
|
G | GA | 10 | a0002c0002t0002g0007a0002c0002t0002g0049a0002c0002t0002g0314others(7): Show | 14 | HG00099.hp2 HG02004.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+307_1596+308i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767777 | ||||||
chr16:767777
|
G | GAGGA | 6 | a0004c0006t0001g0224a0004c0006t0001g0267a0004c0006t0001g0346others(3): Show | 6 | HG00558.hp1 HG00642.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+307_1596+308i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767777 | ||||||
chr16:767778
|
G | A | 3 | a0002c0002t0002g0295a0002c0003t0002g0253a0007c0016t0001g0043 | 3 | HG02280.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+308G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767778 | ||||||
chr16:767778
|
G | C | 1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+308G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767778 | ||||||
chr16:767778
|
G | GGTCGCGT others(280): Show |
1 | a0004c0017t0001g0264 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1596+309_1596+310i others(289): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767778 | |||||
chr16:767779
|
G | GGGGCGAG others(4): Show |
1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+311_1596+312i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767779 | |||||
chr16:767779
|
G | GT | 3 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304 | 3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+309_1596+310i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767779 | ||||||
chr16:767779
|
G | GTCGCGT | 14 | a0002c0002t0002g0335a0002c0015t0003g0255a0002c0015t0003g0256others(11): Show | 16 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+309_1596+310i others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767779 | ||||||
chr16:767781
|
G | C | 55 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0084others(52): Show | 66 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1596+311G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | ||||||
chr16:767781
|
G | GGCGTGTG others(8): Show |
1 | a0002c0003t0004g0217 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1596+311_1596+312i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | ||||||
chr16:767781
|
G | T | 3 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304 | 3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+311G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | ||||||
chr16:767781
|
GA | G | 3 | a0002c0002t0002g0191a0003c0004t0003g0226a0008c0009t0002g0257 | 3 | HG03209.hp2 NA18941.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+312delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | ||||||
chr16:767782
|
A | C | 94 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0084others(91): Show | 98 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1596+312A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | ||||||
chr16:767782
|
A | G | 6 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304others(3): Show | 6 | HG01978.hp1 HG02027.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+312A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | ||||||
chr16:767782
|
A | T | 4 | a0003c0004t0003g0291a0007c0012t0001g0004a0007c0012t0001g0245others(1): Show | 6 | HG02055.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+312A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | ||||||
chr16:767782
|
AG | A | 34 | a0001c0001t0001g0134a0002c0002t0002g0001a0002c0002t0002g0017others(31): Show | 43 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1596+313delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | ||||||
chr16:767782
|
AGCGTGGG others(31): Show |
A | 1 | a0001c0001t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1596+323_1596+360d others(40): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767782 | |||||
chr16:767783
|
G | A | 2 | a0002c0002t0002g0193a0028c0044t0002g0250 | 2 | NA18990.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1596+313G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767783 | ||||||
chr16:767783
|
GC | G | 18 | a0002c0002t0002g0335a0002c0015t0003g0255a0002c0015t0003g0256others(15): Show | 22 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596+314delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767783 | ||||||
chr16:767784
|
C | A | 3 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304 | 3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+314C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767784 | ||||||
chr16:767784
|
C | T | 17 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0084others(14): Show | 19 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+314C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767784 | ||||||
chr16:767785
|
G | A | 4 | a0004c0006t0001g0224a0004c0021t0001g0298a0016c0028t0001g0187others(1): Show | 4 | HG00558.hp1 HG01099.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+315G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767785 | ||||||
chr16:767786
|
T | A | 21 | a0002c0002t0002g0295a0002c0002t0002g0335a0002c0003t0002g0253others(18): Show | 25 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+316T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767786 | ||||||
chr16:767786
|
T | G | 5 | a0001c0001t0010g0140a0001c0008t0001g0302a0001c0008t0001g0304others(2): Show | 5 | HG00642.hp1 HG02027.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+316T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767786 | ||||||
chr16:767786
|
T | TG | 50 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0084others(47): Show | 56 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1596+322dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGAGGGG others(8): Show |
1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+318_1596+319i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGGG others(7): Show |
1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGGG others(310): Show |
1 | a0001c0008t0001g0300 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(319): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGGG others(111): Show |
1 | a0002c0003t0002g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGGG others(109): Show |
1 | a0002c0003t0004g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(118): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGGG others(70): Show |
1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(79): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGGG others(221): Show |
1 | a0001c0001t0001g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(230): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGGGGGTG others(19): Show |
1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+321_1596+322i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767786
|
T | TGTGGGGG others(9): Show |
1 | a0002c0003t0004g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1596+317_1596+318i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | |||||
chr16:767787
|
G | GGA | 10 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(7): Show | 10 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+318_1596+319i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767787 | |||||
chr16:767789
|
G | A | 42 | a0001c0001t0001g0134a0002c0002t0002g0001a0002c0002t0002g0017others(39): Show | 53 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1596+319G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767789 | ||||||
chr16:767789
|
G | C | 1 | a0007c0016t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+319G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767789 | ||||||
chr16:767790
|
G | A | 6 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(3): Show | 6 | HG02155.hp2 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+320G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767790 | ||||||
chr16:767790
|
G | C | 3 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+320G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767790 | ||||||
chr16:767790
|
G | T | 12 | a0001c0001t0001g0223a0001c0022t0001g0270a0002c0002t0002g0054others(9): Show | 13 | HG01361.hp1 HG01981.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+320G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767790 | ||||||
chr16:767791
|
G | A | 1 | a0007c0016t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+321G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | ||||||
chr16:767791
|
G | C | 38 | a0001c0001t0001g0223a0001c0001t0010g0140a0001c0008t0001g0302others(35): Show | 43 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1596+321G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | ||||||
chr16:767791
|
G | GGCGTGGA others(442): Show |
1 | a0001c0001t0001g0114 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1596+348_1596+349i others(451): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGCGTGGA others(88): Show |
2 | a0001c0001t0001g0179a0001c0008t0001g0303 | 2 | HG02040.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1596+348_1596+349i others(97): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGCGTGGA others(89): Show |
1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1596+348_1596+349i others(98): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGCGTGGA others(142): Show |
1 | a0001c0001t0001g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1596+349_1597-412d others(151): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGCGAGT others(74): Show |
1 | a0014c0024t0013g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(83): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGCGCAT others(34): Show |
1 | a0002c0003t0004g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGGCGCA others(22): Show |
1 | a0001c0001t0011g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGGCGCG others(78): Show |
1 | a0002c0002t0002g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(87): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGGGCGC others(105): Show |
1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(114): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGGGCGC others(283): Show |
1 | a0001c0001t0001g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(292): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTC | 37 | a0001c0001t0001g0134a0002c0002t0002g0001a0002c0002t0002g0017others(34): Show | 46 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1596+322_1596+323i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGCGT others(121): Show |
1 | a0001c0001t0001g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(83): Show |
1 | a0002c0003t0004g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(125): Show |
1 | a0002c0002t0002g0329 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(82): Show |
1 | a0002c0002t0002g0324 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(91): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(126): Show |
1 | a0002c0002t0002g0188 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(135): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(125): Show |
2 | a0002c0002t0002g0321a0002c0002t0002g0323 | 2 | NA18940.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1596+322_1596+323i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(84): Show |
3 | a0002c0003t0004g0231a0002c0003t0004g0232a0002c0003t0004g0233 | 3 | HG02818.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1596+322_1596+323i others(93): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(123): Show |
1 | a0002c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(173): Show |
1 | a0002c0003t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(182): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(216): Show |
1 | a0008c0009t0002g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(225): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(204): Show |
1 | a0005c0045t0001g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(213): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(235): Show |
3 | a0001c0022t0001g0178a0004c0006t0001g0251a0019c0032t0001g0177 | 3 | HG03669.hp1 HG04204.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1596+322_1596+323i others(244): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(266): Show |
1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(275): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(312): Show |
1 | a0020c0033t0001g0342 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(321): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(296): Show |
1 | a0004c0006t0001g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(305): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(58): Show |
1 | a0006c0007t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GGGTGTGG others(248): Show |
1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(257): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | |||||
chr16:767791
|
G | GTGCGTGG others(227): Show |
3 | a0006c0007t0001g0008a0006c0007t0001g0023a0021c0043t0001g0008 | 3 | HG02451.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1596+321_1596+322i others(236): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | ||||||
chr16:767791
|
G | GTGCGTGG others(228): Show |
1 | a0006c0007t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1596+321_1596+322i others(237): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | ||||||
chr16:767791
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0073a0003c0004t0003g0226others(7): Show | 14 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+321G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | ||||||
chr16:767793
|
C | A | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+323C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767793 | ||||||
chr16:767793
|
C | CGCGTG | 4 | a0002c0002t0002g0314a0002c0002t0002g0336a0002c0002t0012g0315others(1): Show | 4 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+324_1596+325i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767793 | |||||
chr16:767793
|
C | G | 5 | a0002c0002t0002g0337a0003c0004t0003g0271a0007c0012t0001g0004others(2): Show | 7 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+323C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767793 | ||||||
chr16:767793
|
C | T | 16 | a0001c0001t0001g0283a0001c0008t0001g0300a0002c0003t0002g0247others(13): Show | 16 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+323C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767793 | ||||||
chr16:767794
|
G | A | 2 | a0002c0002t0002g0295a0002c0003t0002g0253 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+324G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767794 | ||||||
chr16:767794
|
G | GCGTGGAG others(175): Show |
1 | a0002c0002t0002g0328 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1596+324_1596+325i others(184): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767794 | ||||||
chr16:767795
|
T | A | 4 | a0002c0002t0002g0314a0002c0002t0002g0336a0002c0002t0012g0315others(1): Show | 4 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+325T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767795 | ||||||
chr16:767795
|
T | C | 1 | a0002c0002t0002g0337 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+325T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767795 | ||||||
chr16:767795
|
T | G | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+325T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767795 | ||||||
chr16:767796
|
G | GC | 3 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+326_1596+327i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767796 | ||||||
chr16:767797
|
G | C | 1 | a0002c0002t0002g0337 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+327G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767797 | ||||||
chr16:767798
|
A | C | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+328A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767798 | ||||||
chr16:767798
|
A | T | 4 | a0001c0001t0001g0093a0007c0012t0001g0004a0007c0012t0001g0245others(1): Show | 6 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+328A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767798 | ||||||
chr16:767798
|
AGG | A | 1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+329_1596+330d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767798 | ||||||
chr16:767799
|
G | T | 1 | a0002c0002t0002g0337 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+329G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767799 | ||||||
chr16:767800
|
G | C | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+330G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767800 | ||||||
chr16:767800
|
GA | G | 18 | a0001c0001t0001g0062a0001c0001t0001g0161a0001c0001t0001g0223others(15): Show | 18 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+331delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767800 | ||||||
chr16:767801
|
A | AGGGGCGC others(129): Show |
1 | a0023c0037t0001g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1596+348_1596+349i others(138): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767801 | |||||
chr16:767801
|
A | AGGGGGCG others(75): Show |
1 | a0001c0001t0001g0339 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1596+335_1596+336i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767801 | |||||
chr16:767801
|
A | ATG | 5 | a0002c0002t0002g0235a0002c0002t0002g0308a0002c0002t0002g0309others(2): Show | 5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+331_1596+332i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767801 | ||||||
chr16:767801
|
A | C | 1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+331A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767801 | ||||||
chr16:767801
|
A | G | 18 | a0001c0001t0001g0063a0001c0001t0001g0093a0001c0001t0001g0283others(15): Show | 18 | HG00423.hp1 HG02132.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+331A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767801 | ||||||
chr16:767806
|
C | CGCGTGGA others(731): Show |
1 | a0001c0001t0001g0097 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1596+345_1596+346i others(740): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | |||||
chr16:767806
|
C | CGCGTGGA others(17): Show |
1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1596+348_1596+349i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | |||||
chr16:767806
|
C | CGCGTGGA others(195): Show |
1 | a0025c0042t0001g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596+362_1596+363i others(204): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | |||||
chr16:767806
|
C | CGCGTGGA others(30): Show |
1 | a0005c0005t0001g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1596+362_1596+363i others(39): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | |||||
chr16:767806
|
C | G | 8 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(5): Show | 8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+336C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767806 | ||||||
chr16:767806
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0161a0002c0003t0004g0234others(1): Show | 6 | HG02451.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+336C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767806 | ||||||
chr16:767808
|
C | A | 5 | a0002c0003t0004g0213a0006c0007t0001g0008a0006c0007t0001g0023others(2): Show | 5 | HG01943.hp2 HG02451.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+338C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767808 | ||||||
chr16:767808
|
C | CATGGGGG others(3): Show |
4 | a0002c0002t0002g0314a0002c0002t0002g0336a0002c0002t0012g0315others(1): Show | 4 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+338_1596+339i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767808 | ||||||
chr16:767808
|
C | CGTGGAGG others(98): Show |
1 | a0001c0001t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | |||||
chr16:767808
|
C | CGTGGAGG others(8): Show |
1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+349_1596+350i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | |||||
chr16:767808
|
C | CGTGGAGG others(23): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0244 | 2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1596+349_1596+350i others(32): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | |||||
chr16:767808
|
C | CGTGGAGG others(192): Show |
1 | a0008c0009t0002g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1596+349_1596+350i others(201): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | |||||
chr16:767808
|
C | CGTGGGGG others(3): Show |
1 | a0004c0006t0001g0266 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1596+342_1596+343i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | |||||
chr16:767808
|
C | T | 16 | a0001c0001t0001g0086a0001c0001t0001g0156a0001c0001t0001g0204others(13): Show | 18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+338C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767808 | ||||||
chr16:767809
|
G | A | 2 | a0002c0003t0002g0247a0002c0003t0002g0249 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1596+339G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767809 | ||||||
chr16:767810
|
T | C | 1 | a0006c0007t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1596+340T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767810 | ||||||
chr16:767810
|
TGGAG | T | 5 | a0001c0001t0001g0223a0003c0004t0003g0269a0004c0006t0001g0240others(2): Show | 5 | HG00423.hp2 HG03471.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+343_1596+346d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767810 | |||||
chr16:767812
|
G | GGGGTGCG others(1): Show |
4 | a0002c0003t0002g0247a0002c0003t0002g0249a0004c0006t0001g0181others(1): Show | 4 | HG02080.hp2 HG02647.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+342_1596+343i others(10): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767812 | ||||||
chr16:767813
|
A | AG | 15 | a0001c0001t0001g0105a0001c0001t0001g0149a0001c0001t0001g0168others(12): Show | 15 | HG00408.hp1 HG01169.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+349dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767813 | |||||
chr16:767813
|
A | AGGGGGGG others(166): Show |
1 | a0009c0011t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1596+349_1596+350i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767813 | |||||
chr16:767813
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0073a0002c0003t0002g0247others(7): Show | 13 | HG01109.hp2 HG02055.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+343A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767813 | ||||||
chr16:767813
|
AG | A | 6 | a0002c0002t0002g0189a0002c0002t0002g0294a0002c0002t0002g0312others(3): Show | 6 | HG00733.hp2 HG02080.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+349delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767813 | |||||
chr16:767815
|
G | C | 1 | a0007c0016t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+345G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | ||||||
chr16:767815
|
G | GA | 21 | a0001c0001t0001g0161a0003c0004t0003g0015a0003c0004t0003g0016others(18): Show | 23 | HG00558.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+345_1596+346i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | ||||||
chr16:767815
|
G | GAGGA | 5 | a0000c0039t0008g0146a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 7 | HG00423.hp1 HG01192.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+345_1596+346i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | ||||||
chr16:767815
|
G | GAGGGGCG others(69): Show |
1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+345_1596+346i others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | ||||||
chr16:767815
|
G | GAGGGGCG others(171): Show |
1 | a0004c0006t0001g0350 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1596+345_1596+346i others(180): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | ||||||
chr16:767815
|
G | GGGGCCGT others(75): Show |
1 | a0009c0011t0001g0340 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1596+348_1596+349i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | |||||
chr16:767815
|
G | GGGGCGCG others(7): Show |
6 | a0001c0022t0001g0178a0004c0006t0001g0185a0004c0006t0001g0262others(3): Show | 6 | HG03669.hp1 HG04184.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+348_1596+349i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | |||||
chr16:767815
|
G | GGGGGCGC others(50): Show |
1 | a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1596+356_1596+357i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | |||||
chr16:767815
|
G | GGGGGCGC others(189): Show |
1 | a0001c0001t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(198): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | |||||
chr16:767818
|
G | A | 3 | a0007c0012t0001g0004a0007c0012t0001g0245a0007c0012t0001g0246 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+348G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767818 | ||||||
chr16:767819
|
G | C | 23 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0065others(20): Show | 24 | HG00597.hp1 HG00597.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+349G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767819 | ||||||
chr16:767820
|
C | A | 13 | a0001c0001t0001g0042a0001c0001t0001g0076a0001c0001t0001g0339others(10): Show | 13 | HG02040.hp1 HG02486.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+350C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767820 | ||||||
chr16:767820
|
C | CGCGTGGG others(288): Show |
1 | a0001c0001t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596+372_1596+373i others(297): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767820 | |||||
chr16:767820
|
C | T | 9 | a0001c0001t0001g0090a0001c0001t0001g0223a0002c0002t0002g0335others(6): Show | 9 | HG00423.hp2 HG02132.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+350C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767820 | ||||||
chr16:767821
|
G | A | 2 | a0004c0006t0001g0181a0004c0006t0001g0265 | 2 | HG02080.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596+351G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767821 | ||||||
chr16:767822
|
C | CGTGGGGG others(28): Show |
1 | a0001c0001t0001g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1596+362_1596+363i others(37): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767822 | |||||
chr16:767822
|
C | CGTGGGGG others(27): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(36): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767822 | |||||
chr16:767822
|
C | CGTGGGGG others(3): Show |
1 | a0001c0001t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1596+359_1596+360i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767822 | |||||
chr16:767822
|
C | T | 24 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0065others(21): Show | 25 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1596+352C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767822 | ||||||
chr16:767823
|
G | A | 5 | a0000c0039t0008g0146a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 7 | HG00423.hp1 HG01192.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+353G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767823 | ||||||
chr16:767823
|
GTGGGGGG others(6): Show |
G | 2 | a0002c0003t0004g0218a0002c0003t0004g0219 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1596+362_1596+374d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767823 | |||||
chr16:767824
|
T | G | 1 | a0002c0002t0002g0335 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1596+354T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767824 | ||||||
chr16:767824
|
T | TGGGGGGG others(163): Show |
1 | a0001c0001t0001g0355 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1596+362_1596+363i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767824 | |||||
chr16:767825
|
G | A | 2 | a0001c0001t0001g0103a0002c0002t0002g0335 | 2 | HG00099.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1596+355G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767825 | ||||||
chr16:767825
|
G | GGAGGA | 19 | a0001c0001t0001g0161a0001c0022t0001g0178a0002c0002t0002g0189others(16): Show | 19 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+356_1596+357i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767825
|
G | GGAGGAGG others(255): Show |
1 | a0016c0028t0001g0187 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1596+356_1596+357i others(264): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767825
|
G | GGAGGAGG others(71): Show |
1 | a0004c0006t0001g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1596+356_1596+357i others(80): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767825
|
G | GGAGGGGG others(112): Show |
2 | a0008c0009t0002g0044a0008c0009t0002g0045 | 2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1596+356_1596+357i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767825
|
G | GGAGGGGG others(115): Show |
1 | a0008c0009t0002g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+356_1596+357i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767825
|
G | GGAGGGGG others(57): Show |
1 | a0008c0009t0002g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1596+356_1596+357i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767825
|
G | GGGGGGGT others(26): Show |
1 | a0028c0044t0002g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(35): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | |||||
chr16:767826
|
G | GA | 30 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0348others(27): Show | 37 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1596+356_1596+357i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767826 | ||||||
chr16:767826
|
G | GAGGGGGG others(9): Show |
3 | a0001c0001t0001g0242a0001c0001t0001g0243a0016c0029t0001g0225 | 3 | HG01884.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+356_1596+357i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767826 | ||||||
chr16:767826
|
G | GGGGGGCG others(4): Show |
1 | a0001c0041t0001g0152 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | |||||
chr16:767826
|
G | GGGGGGGT others(5): Show |
4 | a0001c0022t0001g0270a0002c0002t0002g0197a0002c0015t0003g0255others(1): Show | 4 | HG01361.hp1 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+362_1596+363i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | |||||
chr16:767826
|
G | GGGGGGGT others(29): Show |
1 | a0014c0047t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1596+362_1596+363i others(38): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | |||||
chr16:767826
|
G | GGGGGGTG others(4): Show |
38 | a0002c0002t0002g0001a0002c0002t0002g0017a0002c0002t0002g0018others(35): Show | 47 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | |||||
chr16:767826
|
G | GGGGGGTG others(28): Show |
2 | a0003c0004t0003g0019a0003c0004t0003g0352 | 3 | HG01884.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(37): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | |||||
chr16:767827
|
G | A | 15 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(12): Show | 16 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1596+357G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767827 | ||||||
chr16:767827
|
G | GGGGGTGT others(3): Show |
2 | a0002c0002t0002g0307a0002c0002t0002g0338 | 2 | NA18953.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767827 | |||||
chr16:767827
|
G | GGGGGTGT others(14): Show |
1 | a0002c0002t0002g0321 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(23): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767827 | |||||
chr16:767827
|
G | GGGGGTGT others(188): Show |
1 | a0002c0002t0002g0318 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(197): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767827 | |||||
chr16:767828
|
G | A | 23 | a0001c0001t0001g0103a0001c0001t0001g0161a0001c0022t0001g0178others(20): Show | 23 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+358G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767828 | ||||||
chr16:767828
|
G | GGGGCGTG others(5): Show |
2 | a0001c0001t0001g0341a0004c0017t0001g0263 | 2 | HG00597.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(23): Show |
1 | a0001c0001t0001g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(32): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(175): Show |
1 | a0001c0001t0001g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(184): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(22): Show |
7 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0001g0148others(4): Show | 7 | HG02056.hp1 HG02155.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(250): Show |
1 | a0001c0001t0001g0133 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(259): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(117): Show |
1 | a0001c0001t0001g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(126): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(201): Show |
1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(210): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(79): Show |
1 | a0005c0005t0001g0033 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(292): Show |
1 | a0009c0011t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(301): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(124): Show |
1 | a0001c0001t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGCGTG others(79): Show |
1 | a0000c0039t0008g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGTGTG others(37): Show |
1 | a0001c0001t0001g0062 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGTGTG others(75): Show |
1 | a0001c0001t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGTGTG others(76): Show |
1 | a0002c0002t0002g0007 | 3 | HG02922.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(85): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGGTGTG others(154): Show |
1 | a0001c0001t0001g0130 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(163): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGGTGTGG others(46): Show |
1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+360_1596+361i others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767828
|
G | GGTGCGTG others(278): Show |
1 | a0004c0006t0001g0266 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1596+359_1596+360i others(287): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | |||||
chr16:767830
|
GGGCGCAT others(35): Show |
G | 1 | a0006c0010t0001g0239 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1596+362_1596+403d others(44): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767830 | |||||
chr16:767831
|
G | C | 2 | a0001c0001t0001g0076a0005c0005t0001g0025 | 2 | HG03492.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1596+361G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | ||||||
chr16:767831
|
G | GA | 1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | ||||||
chr16:767831
|
G | GC | 8 | a0001c0001t0001g0116a0001c0001t0001g0252a0002c0003t0001g0102others(5): Show | 9 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | ||||||
chr16:767831
|
G | GT | 6 | a0001c0001t0001g0131a0001c0001t0001g0134a0006c0010t0001g0013others(3): Show | 7 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | ||||||
chr16:767831
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+361G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | ||||||
chr16:767832
|
G | C | 10 | a0005c0005t0001g0009a0005c0005t0001g0022a0005c0005t0001g0031others(7): Show | 11 | HG00738.hp2 HG01243.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+362G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767832 | ||||||
chr16:767833
|
C | A | 3 | a0002c0003t0004g0234a0003c0004t0003g0226a0009c0011t0001g0340 | 3 | HG03130.hp2 NA19083.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+363C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767833 | ||||||
chr16:767833
|
C | T | 29 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0116others(26): Show | 31 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1596+363C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767833 | ||||||
chr16:767834
|
G | A | 24 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0090others(21): Show | 24 | HG00099.hp2 HG00558.hp2 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.1596+364G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767834 | ||||||
chr16:767835
|
C | G | 20 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0116others(17): Show | 22 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596+365C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767835 | ||||||
chr16:767835
|
C | T | 8 | a0002c0003t0002g0247a0002c0003t0002g0249a0002c0034t0003g0259others(5): Show | 9 | HG00738.hp2 HG02080.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+365C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767835 | ||||||
chr16:767836
|
A | G | 76 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0084others(73): Show | 86 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1596+366A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767836 | ||||||
chr16:767837
|
T | G | 22 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0116others(19): Show | 25 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+367T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767837 | ||||||
chr16:767837
|
T | TG | 35 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0077others(32): Show | 35 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1596+374dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | |||||
chr16:767837
|
T | TGGA | 10 | a0001c0001t0001g0090a0003c0004t0003g0019a0003c0004t0003g0269others(7): Show | 11 | HG00423.hp2 HG01884.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+369_1596+370i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | |||||
chr16:767837
|
T | TGGGGGTG others(4): Show |
1 | a0002c0002t0002g0323 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1596+372_1596+373i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | |||||
chr16:767837
|
T | TGGGGGTG others(5): Show |
4 | a0002c0002t0002g0196a0002c0002t0002g0332a0002c0002t0002g0343others(1): Show | 4 | HG00621.hp1 HG00621.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+372_1596+373i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | |||||
chr16:767838
|
G | GA | 7 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0252others(4): Show | 7 | HG00738.hp1 HG01257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+368_1596+369i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767838 | ||||||
chr16:767838
|
G | GGAGGA | 7 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0341others(4): Show | 8 | HG00597.hp2 HG01109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+369_1596+370i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767838 | |||||
chr16:767839
|
G | GA | 5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+369_1596+370i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767839 | ||||||
chr16:767840
|
G | A | 13 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(10): Show | 13 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+370G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767840 | ||||||
chr16:767841
|
G | C | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+371G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767841 | ||||||
chr16:767843
|
G | A | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+373G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767843 | ||||||
chr16:767843
|
G | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0076others(31): Show | 39 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1596+373G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767843 | ||||||
chr16:767843
|
G | GGTC | 12 | a0002c0002t0002g0235a0002c0002t0002g0295a0002c0002t0002g0308others(9): Show | 12 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+374_1596+375i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767843 | |||||
chr16:767843
|
G | T | 41 | a0001c0001t0001g0339a0001c0022t0001g0270a0002c0002t0002g0001others(38): Show | 50 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1596+373G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767843 | ||||||
chr16:767844
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+374G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767844 | ||||||
chr16:767845
|
C | G | 4 | a0002c0003t0002g0247a0002c0003t0002g0249a0002c0034t0003g0259others(1): Show | 4 | HG02647.hp1 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+375C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767845 | ||||||
chr16:767845
|
C | T | 38 | a0001c0001t0001g0065a0001c0001t0001g0087a0001c0001t0001g0091others(35): Show | 41 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1596+375C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767845 | ||||||
chr16:767846
|
G | C | 7 | a0002c0003t0002g0247a0002c0003t0002g0249a0002c0015t0003g0066others(4): Show | 11 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+376G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767846 | ||||||
chr16:767846
|
GT | G | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+377delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767846 | ||||||
chr16:767847
|
T | C | 8 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0348others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+377T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767847 | ||||||
chr16:767847
|
T | G | 5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+377T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767847 | ||||||
chr16:767847
|
TGGAG | T | 5 | a0001c0001t0001g0131a0006c0010t0001g0013a0006c0010t0001g0236others(2): Show | 6 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+380_1596+383d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767847 | |||||
chr16:767848
|
G | C | 5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+378G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767848 | ||||||
chr16:767848
|
GGA | G | 32 | a0001c0001t0001g0093a0001c0001t0001g0348a0001c0001t0001g0349others(29): Show | 41 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1596+380_1596+381d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767848 | |||||
chr16:767849
|
G | C | 6 | a0001c0001t0001g0242a0001c0001t0001g0243a0002c0003t0002g0247others(3): Show | 6 | HG02647.hp1 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+379G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | ||||||
chr16:767849
|
G | GGGGTGTG others(141): Show |
1 | a0001c0001t0001g0134 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1596+379_1596+380i others(150): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | ||||||
chr16:767849
|
G | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0090others(15): Show | 19 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+379G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | ||||||
chr16:767849
|
GA | G | 6 | a0001c0022t0001g0270a0002c0002t0002g0192a0002c0002t0002g0311others(3): Show | 6 | HG01192.hp1 HG01361.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+380delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | ||||||
chr16:767850
|
A | AG | 10 | a0001c0001t0001g0092a0001c0001t0001g0176a0001c0001t0001g0252others(7): Show | 10 | HG00738.hp1 HG01106.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+386dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767850
|
A | AGGAGGAG others(72): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767850
|
A | AGGAGGGG others(97): Show |
1 | a0010c0013t0007g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(106): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767850
|
A | AGGAGGGG others(98): Show |
2 | a0010c0013t0006g0209a0010c0013t0006g0210 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1596+382_1596+383i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767850
|
A | AGGAGGGG others(98): Show |
1 | a0010c0013t0007g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1596+382_1596+383i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767850
|
A | AGGGGGGC others(44): Show |
6 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0272others(3): Show | 7 | HG01106.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+386_1596+387i others(53): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767850
|
A | G | 25 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0090others(22): Show | 26 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+380A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767850 | ||||||
chr16:767850
|
A | T | 6 | a0002c0002t0002g0307a0002c0015t0003g0066a0002c0015t0003g0174others(3): Show | 10 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+380A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767850 | ||||||
chr16:767850
|
AG | A | 5 | a0006c0007t0001g0254a0007c0012t0001g0004a0007c0012t0001g0245others(2): Show | 9 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+386delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | |||||
chr16:767851
|
G | GGAGGGGC others(186): Show |
2 | a0004c0006t0001g0181a0004c0006t0001g0265 | 2 | HG02080.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596+382_1596+383i others(195): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGGCGCGT others(3): Show |
1 | a0002c0002t0002g0317 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1596+383_1596+384i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGGGCGCG others(4): Show |
1 | a0002c0002t0002g0326 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1596+384_1596+385i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGGGGCCG others(3): Show |
2 | a0001c0001t0001g0076a0005c0005t0001g0025 | 2 | HG03492.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1596+385_1596+386i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGGGGGAG others(3): Show |
1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+386_1596+387i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGGGGGCG others(45): Show |
1 | a0001c0001t0001g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1596+386_1596+387i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGGGGGCG others(72): Show |
1 | a0001c0001t0011g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+386_1596+387i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | GGTGTGTG others(121): Show |
1 | a0001c0001t0001g0116 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | |||||
chr16:767851
|
G | T | 10 | a0001c0001t0001g0093a0001c0001t0001g0134a0001c0001t0001g0242others(7): Show | 10 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+381G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767851 | ||||||
chr16:767852
|
G | GA | 22 | a0001c0001t0001g0339a0002c0002t0002g0235a0002c0002t0002g0295others(19): Show | 23 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+382_1596+383i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767852 | ||||||
chr16:767852
|
G | GAGGAGGG others(45): Show |
1 | a0002c0003t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767852 | ||||||
chr16:767852
|
G | GAGGGGCG others(166): Show |
1 | a0005c0005t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767852 | ||||||
chr16:767852
|
G | GGGGGCGC others(92): Show |
1 | a0001c0001t0001g0120 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1596+386_1596+387i others(101): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767852 | |||||
chr16:767852
|
GGGGGTGC others(8): Show |
G | 1 | a0005c0005t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1596+387_1596+401d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767852 | |||||
chr16:767853
|
G | GAGGCGCG others(197): Show |
1 | a0006c0007t0001g0014 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1596+383_1596+384i others(206): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767853 | ||||||
chr16:767853
|
G | GAGGCGCG others(198): Show |
1 | a0006c0007t0001g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1596+383_1596+384i others(207): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767853 | ||||||
chr16:767853
|
G | T | 1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+383G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767853 | ||||||
chr16:767856
|
G | C | 1 | a0003c0004t0003g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+386G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767856 | ||||||
chr16:767856
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1596+386G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767856 | ||||||
chr16:767856
|
GT | G | 4 | a0002c0015t0003g0174a0003c0004t0003g0002a0003c0004t0003g0277others(1): Show | 8 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+387delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767856 | ||||||
chr16:767857
|
T | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0341 | 2 | HG00597.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1596+387T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767857 | ||||||
chr16:767857
|
T | C | 120 | a0000c0039t0008g0146a0001c0001t0001g0005a0001c0001t0001g0065others(117): Show | 139 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1596+387T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767857 | ||||||
chr16:767857
|
T | G | 24 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0116others(21): Show | 24 | HG00621.hp1 HG00621.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+387T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767857 | ||||||
chr16:767857
|
T | TGCGTGGA others(8): Show |
1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+400_1596+414d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767857 | |||||
chr16:767857
|
T | TGCGTGGA others(61): Show |
1 | a0002c0003t0004g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+411_1596+412i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767857 | |||||
chr16:767857
|
TGCGTGGA others(8): Show |
T | 2 | a0001c0001t0001g0288a0024c0040t0001g0287 | 2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1596+400_1596+414d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767857 | |||||
chr16:767858
|
G | A | 3 | a0001c0022t0001g0270a0007c0016t0005g0012a0007c0016t0005g0229 | 4 | HG01361.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+388G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767858 | ||||||
chr16:767859
|
C | A | 1 | a0006c0007t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1596+389C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767859 | ||||||
chr16:767859
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0134 | 2 | NA18939.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1596+389C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767859 | ||||||
chr16:767861
|
TG | T | 4 | a0002c0002t0002g0317a0002c0002t0002g0332a0002c0002t0002g0343others(1): Show | 4 | HG00621.hp1 HG00621.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+393delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767861 | |||||
chr16:767863
|
G | T | 2 | a0002c0002t0002g0196a0002c0002t0002g0326 | 2 | HG01256.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1596+393G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767863 | ||||||
chr16:767863
|
GAGGAGGG others(51): Show |
G | 4 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(1): Show | 5 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+394_1596+451d others(60): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767863 | ||||||
chr16:767864
|
A | AGGGGGCA others(3): Show |
1 | a0002c0002t0002g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1596+396_1596+397i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | |||||
chr16:767864
|
A | AGGGGGCA others(79): Show |
1 | a0002c0002t0002g0312 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1596+396_1596+397i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | |||||
chr16:767864
|
A | AGGGGGCA others(106): Show |
1 | a0002c0002t0002g0007 | 3 | HG02922.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1596+396_1596+397i others(115): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | |||||
chr16:767864
|
A | AGGGGGCA others(202): Show |
1 | a0002c0003t0002g0074 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1596+396_1596+397i others(211): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | |||||
chr16:767864
|
A | AGGGGGGG others(5): Show |
33 | a0002c0002t0002g0001a0002c0002t0002g0017a0002c0002t0002g0018others(30): Show | 42 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1596+396_1596+397i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | |||||
chr16:767864
|
A | G | 3 | a0001c0001t0001g0107a0002c0002t0002g0196a0002c0002t0002g0326 | 3 | HG01256.hp1 HG01257.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1596+394A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767864 | ||||||
chr16:767864
|
A | T | 4 | a0002c0002t0002g0317a0002c0002t0002g0332a0002c0002t0002g0343others(1): Show | 4 | HG00621.hp1 HG00621.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+394A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767864 | ||||||
chr16:767865
|
G | GGGCGTGG others(40): Show |
1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+396_1596+397i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | |||||
chr16:767865
|
G | GGGGGCAC others(178): Show |
1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1596+396_1596+397i others(187): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | |||||
chr16:767865
|
G | GGGGGCAC others(299): Show |
1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1596+396_1596+397i others(308): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | |||||
chr16:767865
|
GGA | G | 17 | a0000c0039t0008g0146a0001c0001t0001g0241a0001c0001t0001g0244others(14): Show | 17 | HG00099.hp2 HG01192.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+397_1596+398d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | |||||
chr16:767866
|
GA | G | 10 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0134others(7): Show | 10 | HG00738.hp2 HG02486.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+397delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767866 | ||||||
chr16:767867
|
A | AGGGGCGC others(114): Show |
1 | a0030c0048t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1597-451_1597-331d others(123): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | |||||
chr16:767867
|
A | AGGGGCGC others(236): Show |
1 | a0005c0005t0001g0033 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1597-453_1597-452i others(245): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | |||||
chr16:767867
|
A | AGGGGCGC others(31): Show |
1 | a0001c0001t0001g0172 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(40): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | |||||
chr16:767867
|
A | AGGGGCGC others(84): Show |
1 | a0005c0005t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(93): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | |||||
chr16:767867
|
A | AGGGGCGC others(191): Show |
1 | a0005c0005t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+411_1596+412i others(200): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | |||||
chr16:767867
|
A | AGGGGGCG others(24): Show |
1 | a0002c0003t0004g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+401_1596+402i others(33): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | |||||
chr16:767867
|
A | G | 58 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0131others(55): Show | 70 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1596+397A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767867 | ||||||
chr16:767872
|
C | G | 1 | a0003c0004t0003g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+402C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767872 | ||||||
chr16:767873
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0241a0001c0001t0001g0244others(2): Show | 5 | HG02165.hp2 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+403G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767873 | ||||||
chr16:767874
|
C | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0252a0002c0003t0004g0213others(5): Show | 9 | HG00738.hp1 HG01943.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+404C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767874 | ||||||
chr16:767874
|
C | T | 7 | a0001c0022t0001g0270a0002c0003t0002g0248a0002c0015t0003g0255others(4): Show | 7 | HG01361.hp1 HG01981.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+404C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767874 | ||||||
chr16:767876
|
T | C | 7 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(4): Show | 12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+406T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767876 | ||||||
chr16:767876
|
TGGA | T | 16 | a0001c0001t0001g0150a0001c0001t0001g0223a0002c0034t0003g0259others(13): Show | 18 | HG00423.hp2 HG00558.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+415_1596+417d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767876 | |||||
chr16:767877
|
GGA | G | 3 | a0001c0001t0001g0108a0007c0016t0005g0012a0007c0016t0005g0229 | 4 | HG02717.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+409_1596+410d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767877 | |||||
chr16:767879
|
A | AGGAGGGG others(139): Show |
1 | a0004c0021t0001g0345 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1596+414_1596+415i others(148): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767879 | |||||
chr16:767879
|
A | AGGAGGGG others(5): Show |
1 | a0010c0013t0007g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1596+414_1596+415i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767879 | |||||
chr16:767879
|
A | T | 3 | a0001c0022t0001g0270a0002c0015t0003g0255a0002c0015t0003g0256 | 3 | HG01361.hp1 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596+409A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767879 | ||||||
chr16:767879
|
AGGAGGAG others(143): Show |
A | 1 | a0007c0016t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+412_1597-348d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767879 | |||||
chr16:767880
|
G | GGGGGGGG others(276): Show |
1 | a0002c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(285): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | |||||
chr16:767880
|
G | GGGGGGGG others(275): Show |
1 | a0002c0003t0004g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1596+411_1596+412i others(284): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | |||||
chr16:767880
|
G | GGGGGGGG others(390): Show |
1 | a0002c0003t0004g0231 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | |||||
chr16:767880
|
G | GGGGGGGG others(393): Show |
1 | a0002c0003t0004g0232 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(402): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | |||||
chr16:767881
|
G | GGGGGAGC others(40): Show |
1 | a0001c0001t0001g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+411_1596+412i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | ||||||
chr16:767881
|
G | GGGGGGGC others(18): Show |
4 | a0002c0003t0004g0212a0002c0003t0004g0215a0002c0003t0004g0217others(1): Show | 4 | HG01978.hp1 HG02004.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+411_1596+412i others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | ||||||
chr16:767881
|
G | GGGGGGGG others(19): Show |
1 | a0002c0003t0002g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | ||||||
chr16:767881
|
GAGGA | G | 20 | a0001c0001t0001g0071a0001c0001t0001g0131a0001c0001t0001g0241others(17): Show | 24 | HG00639.hp1 HG01891.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+412_1596+415d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | ||||||
chr16:767882
|
A | AGGGGCGC others(17): Show |
1 | a0001c0001t0011g0202 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+414_1596+415i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767882 | |||||
chr16:767882
|
A | AGGGGCGC others(40): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1596+414_1596+415i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767882 | |||||
chr16:767882
|
A | G | 12 | a0001c0001t0001g0120a0001c0001t0001g0148a0001c0001t0001g0252others(9): Show | 12 | HG00597.hp2 HG00738.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+412A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767882 | ||||||
chr16:767882
|
A | T | 6 | a0002c0003t0004g0230a0002c0003t0004g0231a0002c0003t0004g0232others(3): Show | 6 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+412A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767882 | ||||||
chr16:767882
|
AGGAGGGG others(20): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1596+415_1596+441d others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767882 | |||||
chr16:767883
|
G | GGGGCGCG others(4): Show |
5 | a0004c0006t0001g0240a0010c0013t0006g0209a0010c0013t0006g0210others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+414_1596+415i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767883 | |||||
chr16:767883
|
G | GGGGCGCG others(107): Show |
1 | a0002c0002t0002g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1596+414_1596+415i others(116): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767883 | |||||
chr16:767885
|
A | C | 1 | a0002c0002t0002g0189 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1596+415A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767885 | ||||||
chr16:767885
|
A | G | 30 | a0001c0001t0001g0120a0001c0001t0001g0148a0001c0001t0001g0252others(27): Show | 30 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1596+415A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767885 | ||||||
chr16:767885
|
A | T | 2 | a0001c0001t0001g0341a0002c0002t0002g0313 | 2 | HG00597.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+415A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767885 | ||||||
chr16:767886
|
G | C | 1 | a0002c0002t0002g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1596+416G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767886 | ||||||
chr16:767887
|
G | T | 1 | a0002c0002t0002g0189 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1596+417G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767887 | ||||||
chr16:767888
|
G | C | 2 | a0002c0002t0002g0313a0003c0004t0003g0274 | 2 | HG02258.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+418G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767888 | ||||||
chr16:767889
|
G | C | 10 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0041t0001g0152others(7): Show | 10 | HG02280.hp1 HG02486.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+419G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767889 | ||||||
chr16:767889
|
G | GGC | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0003c0004t0003g0226others(2): Show | 5 | HG02630.hp2 NA18952.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+419_1596+420i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767889 | ||||||
chr16:767890
|
C | A | 8 | a0002c0002t0002g0189a0004c0006t0001g0240a0010c0013t0006g0209others(5): Show | 8 | HG01243.hp2 HG02165.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+420C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767890 | ||||||
chr16:767890
|
C | G | 1 | a0001c0001t0001g0341 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596+420C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767890 | ||||||
chr16:767890
|
C | T | 1 | a0002c0002t0002g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1596+420C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767890 | ||||||
chr16:767892
|
C | A | 3 | a0008c0009t0002g0257a0014c0024t0002g0029a0014c0024t0013g0290 | 3 | HG02622.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+422C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | ||||||
chr16:767892
|
C | G | 3 | a0002c0002t0002g0189a0002c0002t0002g0313a0003c0004t0003g0274 | 3 | HG02165.hp2 HG02258.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+422C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | ||||||
chr16:767892
|
C | T | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0131others(7): Show | 10 | HG02280.hp1 HG02647.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+422C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | ||||||
chr16:767892
|
CATGGGGG others(3): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+423_1596+432d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | ||||||
chr16:767893
|
A | G | 56 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0085others(53): Show | 63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1596+423A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767893 | ||||||
chr16:767894
|
T | G | 2 | a0002c0002t0002g0313a0003c0004t0003g0274 | 2 | HG02258.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+424T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767894 | ||||||
chr16:767894
|
T | TG | 12 | a0001c0001t0001g0106a0001c0001t0001g0163a0001c0001t0001g0171others(9): Show | 12 | HG01169.hp1 HG01496.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+431dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767894 | |||||
chr16:767896
|
G | GA | 2 | a0003c0004t0003g0016a0003c0004t0003g0269 | 3 | HG00423.hp2 HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1596+426_1596+427i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767896 | ||||||
chr16:767897
|
G | A | 13 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(10): Show | 18 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+427G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767897 | ||||||
chr16:767900
|
G | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0341a0001c0022t0001g0270others(7): Show | 10 | HG00558.hp2 HG00597.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+430G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767900 | ||||||
chr16:767900
|
G | T | 3 | a0006c0010t0001g0239a0007c0016t0005g0012a0007c0016t0005g0229 | 4 | HG01981.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+430G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767900 | ||||||
chr16:767902
|
T | A | 1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+432T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767902 | ||||||
chr16:767902
|
T | C | 45 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0085others(42): Show | 50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.1596+432T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767902 | ||||||
chr16:767902
|
T | G | 10 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0019others(7): Show | 12 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+432T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767902 | ||||||
chr16:767902
|
T | TGTGGAGG others(7): Show |
1 | a0005c0045t0001g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1596+443_1597-453d others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767902 | |||||
chr16:767904
|
T | A | 10 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0019others(7): Show | 12 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+434T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767904 | ||||||
chr16:767904
|
T | C | 3 | a0008c0009t0002g0257a0014c0024t0002g0029a0014c0024t0013g0290 | 3 | HG02622.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+434T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767904 | ||||||
chr16:767906
|
G | C | 9 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0019others(6): Show | 11 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+436G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767906 | ||||||
chr16:767906
|
G | T | 4 | a0001c0001t0001g0108a0008c0009t0002g0257a0014c0024t0002g0029others(1): Show | 4 | HG02622.hp2 HG03209.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+436G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767906 | ||||||
chr16:767907
|
A | AG | 22 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0070others(19): Show | 26 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+443dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | |||||
chr16:767907
|
A | AGGGGGGC others(366): Show |
1 | a0027c0026t0001g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1596+453_1596+454i others(375): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | |||||
chr16:767907
|
A | AGGGGGGC others(104): Show |
1 | a0001c0001t0001g0281 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1597-453_1597-452i others(113): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | |||||
chr16:767907
|
A | G | 13 | a0001c0001t0001g0108a0003c0004t0003g0015a0003c0004t0003g0016others(10): Show | 15 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596+437A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767907 | ||||||
chr16:767907
|
A | T | 1 | a0003c0004t0003g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1596+437A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767907 | ||||||
chr16:767907
|
AG | A | 7 | a0001c0001t0001g0061a0001c0001t0001g0171a0002c0003t0004g0217others(4): Show | 7 | HG01243.hp2 HG02257.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+443delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | |||||
chr16:767908
|
G | T | 9 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0019others(6): Show | 11 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+438G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767908 | ||||||
chr16:767908
|
GGGGGGCG others(6): Show |
G | 2 | a0002c0002t0002g0333a0005c0005t0001g0039 | 2 | HG01978.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1596+445_1597-452d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767908 | |||||
chr16:767909
|
G | GA | 17 | a0001c0001t0001g0071a0001c0001t0001g0131a0001c0001t0001g0150others(14): Show | 17 | HG00558.hp2 HG01952.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+439_1596+440i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767909 | ||||||
chr16:767912
|
G | C | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+442G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767912 | ||||||
chr16:767913
|
G | C | 1 | a0003c0004t0003g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+443G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767913 | ||||||
chr16:767914
|
C | A | 3 | a0001c0022t0001g0270a0002c0015t0003g0255a0002c0015t0003g0256 | 3 | HG01361.hp1 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596+444C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767914 | ||||||
chr16:767914
|
C | CGCGTGGG others(3): Show |
3 | a0001c0001t0001g0241a0001c0001t0001g0244a0017c0023t0001g0021 | 3 | HG02717.hp1 HG03195.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1596+450_1596+451i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767914 | |||||
chr16:767914
|
C | G | 10 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0019others(7): Show | 12 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+444C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767914 | ||||||
chr16:767914
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0137a0001c0001t0001g0252others(2): Show | 5 | HG00738.hp1 HG01981.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+444C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767914 | ||||||
chr16:767916
|
C | A | 1 | a0016c0029t0001g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+446C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767916 | ||||||
chr16:767916
|
C | CGTGGAGG others(150): Show |
1 | a0002c0002t0002g0334 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1597-453_1597-452i others(159): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767916 | |||||
chr16:767916
|
C | T | 4 | a0002c0003t0002g0268a0007c0016t0005g0012a0007c0016t0005g0229others(1): Show | 5 | HG02717.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+446C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767916 | ||||||
chr16:767916
|
CGTGGAGG others(100): Show |
C | 1 | a0001c0001t0001g0279 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1597-452_1597-346d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767916 | |||||
chr16:767917
|
G | A | 3 | a0008c0009t0002g0257a0014c0024t0002g0029a0014c0024t0013g0290 | 3 | HG02622.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+447G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767917 | ||||||
chr16:767917
|
GT | G | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+448delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767917 | ||||||
chr16:767918
|
T | C | 4 | a0003c0004t0003g0226a0003c0004t0003g0227a0003c0004t0003g0273others(1): Show | 4 | HG02486.hp2 HG02818.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+448T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767918 | ||||||
chr16:767921
|
A | AG | 7 | a0003c0004t0003g0226a0003c0004t0003g0227a0003c0004t0003g0273others(4): Show | 7 | HG02486.hp2 HG02818.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-453dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767921 | |||||
chr16:767921
|
A | AGG | 13 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(10): Show | 17 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1597-454_1597-453d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767921 | |||||
chr16:767921
|
A | G | 18 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0022t0001g0270others(15): Show | 19 | HG01361.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+451A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767921 | ||||||
chr16:767922
|
G | GGA | 26 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0108others(23): Show | 28 | HG00423.hp2 HG00597.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1596+453_1596+454i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767922 | |||||
chr16:767924
|
G | A | 1 | a0002c0003t0004g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+454G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767924 | ||||||
chr16:767925
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1597-454G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767925 | ||||||
chr16:767925
|
GGCA | G | 8 | a0001c0022t0001g0270a0002c0002t0002g0189a0002c0002t0002g0313others(5): Show | 8 | HG01361.hp1 HG02109.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1597-453_1597-451d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767925 | ||||||
chr16:767926
|
GCACGTGG others(6): Show |
G | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1597-451_1597-439d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767926 | |||||
chr16:767927
|
C | CGCATGGG others(3): Show |
1 | a0008c0009t0002g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1597-452_1597-451i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767927 | ||||||
chr16:767927
|
C | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0131a0001c0001t0001g0150others(3): Show | 7 | HG00558.hp2 HG01952.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-452C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767927 | ||||||
chr16:767927
|
CA | C | 5 | a0002c0003t0002g0248a0010c0013t0006g0209a0010c0013t0006g0210others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-451delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767927 | ||||||
chr16:767928
|
A | ACGTGGAG others(112): Show |
1 | a0004c0017t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1597-443_1597-442i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767928 | |||||
chr16:767928
|
A | AG | 5 | a0001c0001t0001g0090a0001c0001t0001g0131a0001c0001t0001g0150others(2): Show | 5 | HG00558.hp2 HG01952.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-451_1597-450i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767928 | ||||||
chr16:767928
|
A | AGCGTGGG others(295): Show |
1 | a0005c0005t0001g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1597-451_1597-450i others(304): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767928 | ||||||
chr16:767928
|
A | G | 69 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0085others(66): Show | 76 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1597-451A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767928 | ||||||
chr16:767929
|
C | A | 9 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(6): Show | 13 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-450C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767929 | ||||||
chr16:767929
|
C | T | 2 | a0002c0002t0002g0189a0002c0002t0002g0313 | 2 | HG02165.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-450C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767929 | ||||||
chr16:767930
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1597-449G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767930 | ||||||
chr16:767932
|
G | GGGGGGGC others(100): Show |
3 | a0008c0009t0002g0044a0008c0009t0002g0045a0008c0009t0002g0046 | 3 | HG01891.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1597-446_1597-445i others(109): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767932 | |||||
chr16:767932
|
G | GGGGGGGC others(101): Show |
1 | a0008c0009t0002g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1597-446_1597-445i others(110): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767932 | |||||
chr16:767933
|
GA | G | 4 | a0010c0013t0006g0209a0010c0013t0006g0210a0010c0013t0007g0207others(1): Show | 4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-445delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767933 | ||||||
chr16:767934
|
A | AG | 30 | a0001c0001t0001g0061a0001c0001t0001g0223a0001c0001t0001g0348others(27): Show | 38 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1597-441dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGG | 9 | a0002c0003t0002g0247a0002c0003t0002g0249a0002c0015t0003g0066others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-442_1597-441d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGAGGAG others(88): Show |
1 | a0022c0036t0001g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1597-443_1597-442i others(97): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGAGGGG others(113): Show |
1 | a0001c0001t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1597-443_1597-442i others(122): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGAGGGG others(230): Show |
1 | a0001c0001t0001g0116 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1597-443_1597-442i others(239): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGGGGGA others(4): Show |
2 | a0002c0003t0004g0217a0002c0034t0003g0259 | 2 | HG02273.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGGGGGA others(87): Show |
1 | a0001c0001t0001g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1597-441_1597-440i others(96): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGGGGGG others(168): Show |
1 | a0002c0003t0004g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1597-441_1597-440i others(177): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | AGGGGGGG others(290): Show |
1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1597-441_1597-440i others(299): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767934
|
A | G | 13 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0090others(10): Show | 13 | HG00558.hp2 HG01257.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1597-445A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767934 | ||||||
chr16:767934
|
A | T | 1 | a0002c0003t0002g0248 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1597-445A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767934 | ||||||
chr16:767934
|
AGGGGTCG others(3): Show |
A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0026others(2): Show | 5 | HG02451.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-442_1597-433d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | |||||
chr16:767935
|
G | GGA | 5 | a0001c0001t0001g0252a0001c0022t0001g0270a0002c0015t0003g0255others(2): Show | 5 | HG00738.hp1 HG01361.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-443_1597-442i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767935
|
G | GGGGGCCG others(62): Show |
1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1597-441_1597-440i others(71): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767935
|
G | GGGGGGAG others(3): Show |
3 | a0001c0001t0001g0134a0001c0041t0001g0152a0004c0017t0001g0263 | 3 | HG03834.hp1 NA18939.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767935
|
G | GGGGGGCG others(121): Show |
2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767935
|
G | GGGGGGGA others(4): Show |
1 | a0001c0001t0001g0341 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1597-441_1597-440i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767935
|
G | GGGGGGGC others(45): Show |
1 | a0017c0023t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1597-441_1597-440i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767935
|
G | GGGGGGGT others(60): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0244 | 2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | |||||
chr16:767936
|
GGGTC | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0131a0001c0001t0001g0150others(1): Show | 4 | HG00558.hp2 HG03669.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-441_1597-438d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767936 | |||||
chr16:767939
|
T | A | 1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-440T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | ||||||
chr16:767939
|
T | C | 5 | a0003c0004t0003g0226a0003c0004t0003g0227a0003c0004t0003g0271others(2): Show | 5 | HG02486.hp2 HG02818.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-440T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | ||||||
chr16:767939
|
T | G | 85 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0107others(82): Show | 94 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1597-440T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | ||||||
chr16:767939
|
T | TCGCGTGG others(496): Show |
1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(505): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767939 | |||||
chr16:767939
|
T | TCGCGTGG others(214): Show |
1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(223): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767939 | |||||
chr16:767939
|
T | TGTGGAGG others(4): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1597-440_1597-439i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | ||||||
chr16:767940
|
C | CCGCGTGG others(4): Show |
1 | a0014c0047t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-439_1597-438i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767940 | ||||||
chr16:767940
|
C | CGCGTGGA others(121): Show |
1 | a0002c0002t0002g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1597-412_1597-411i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767940 | |||||
chr16:767940
|
C | CGCGTGGA others(17): Show |
2 | a0002c0003t0002g0260a0002c0003t0004g0215 | 2 | HG01934.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1597-430_1597-429i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767940 | |||||
chr16:767940
|
C | CGCGTGGA others(180): Show |
1 | a0002c0003t0004g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(189): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767940 | |||||
chr16:767940
|
C | G | 23 | a0001c0001t0001g0134a0001c0001t0001g0241a0001c0001t0001g0242others(20): Show | 24 | HG00597.hp2 HG01243.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597-439C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767940 | ||||||
chr16:767940
|
C | T | 6 | a0001c0001t0001g0076a0002c0003t0004g0219a0005c0005t0001g0009others(3): Show | 7 | HG02622.hp2 HG03209.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-439C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767940 | ||||||
chr16:767941
|
G | A | 1 | a0002c0002t0002g0189 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1597-438G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767941 | ||||||
chr16:767941
|
G | GCGTGGAG others(191): Show |
1 | a0004c0006t0001g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1597-430_1597-429i others(200): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767941 | |||||
chr16:767942
|
C | A | 4 | a0002c0003t0002g0247a0002c0003t0002g0249a0003c0004t0003g0274others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-437C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767942 | ||||||
chr16:767942
|
C | CGTGGAGG others(69): Show |
1 | a0004c0006t0001g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1597-418_1597-417i others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767942 | |||||
chr16:767942
|
C | CGTGGAGG others(115): Show |
1 | a0002c0003t0004g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767942 | |||||
chr16:767942
|
C | G | 1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-437C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767942 | ||||||
chr16:767943
|
G | A | 2 | a0002c0002t0002g0189a0002c0002t0002g0313 | 2 | HG02165.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-436G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767943 | ||||||
chr16:767944
|
T | C | 1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-435T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767944 | ||||||
chr16:767944
|
TG | T | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-433delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767944 | |||||
chr16:767945
|
GGA | G | 6 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(3): Show | 10 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-432_1597-431d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767945 | |||||
chr16:767946
|
G | C | 1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-433G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767946 | ||||||
chr16:767947
|
A | AGGGGGGA others(99): Show |
1 | a0002c0003t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1597-430_1597-429i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767947 | |||||
chr16:767947
|
A | T | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-432A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767947 | ||||||
chr16:767948
|
G | GGGGGGAG others(59): Show |
4 | a0002c0003t0004g0230a0002c0003t0004g0231a0002c0003t0004g0232others(1): Show | 4 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-430_1597-429i others(68): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGAG others(113): Show |
1 | a0002c0003t0004g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(122): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGCG others(111): Show |
1 | a0004c0006t0001g0346 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGCG others(94): Show |
1 | a0004c0006t0001g0265 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1597-430_1597-429i others(103): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGCG others(109): Show |
7 | a0004c0006t0001g0224a0004c0006t0001g0251a0004c0006t0001g0266others(4): Show | 7 | HG00558.hp1 HG03927.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-430_1597-429i others(118): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGCG others(123): Show |
2 | a0019c0032t0001g0177a0020c0033t0001g0342 | 2 | NA18950.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1597-430_1597-429i others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGCG others(110): Show |
2 | a0004c0006t0001g0267a0004c0017t0001g0264 | 2 | HG00642.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1597-430_1597-429i others(119): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | GGGGGGGC others(111): Show |
1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | |||||
chr16:767948
|
G | T | 1 | a0005c0005t0001g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-431G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767948 | ||||||
chr16:767949
|
G | GGGGGAGC others(87): Show |
1 | a0002c0003t0004g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(96): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767949 | ||||||
chr16:767949
|
GA | G | 21 | a0001c0022t0001g0178a0002c0003t0002g0247a0002c0003t0002g0249others(18): Show | 23 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1597-429delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767949 | ||||||
chr16:767950
|
A | AGGGGCGC others(281): Show |
1 | a0001c0001t0001g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(290): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767950 | |||||
chr16:767950
|
A | AGGGGCGC others(41): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG00280.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1597-412_1597-411i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767950 | |||||
chr16:767950
|
A | G | 43 | a0001c0001t0001g0107a0001c0001t0001g0223a0001c0001t0001g0252others(40): Show | 48 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1597-429A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767950 | ||||||
chr16:767955
|
C | A | 1 | a0002c0003t0004g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1597-424C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767955 | ||||||
chr16:767955
|
C | G | 2 | a0001c0001t0001g0199a0005c0005t0001g0025 | 2 | NA18949.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1597-424C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767955 | ||||||
chr16:767955
|
C | T | 1 | a0002c0002t0002g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1597-424C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767955 | ||||||
chr16:767955
|
CGCGTGGA others(17): Show |
C | 1 | a0002c0003t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1597-411_1597-388d others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767955 | |||||
chr16:767956
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1597-423G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767956 | ||||||
chr16:767957
|
C | A | 2 | a0001c0001t0001g0252a0016c0029t0001g0225 | 2 | HG00738.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1597-422C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767957 | ||||||
chr16:767957
|
C | CGTGGGGG others(3): Show |
3 | a0001c0022t0001g0178a0007c0012t0001g0004a0007c0012t0001g0245 | 5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-418_1597-417i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767957 | |||||
chr16:767958
|
G | A | 14 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(11): Show | 18 | HG00639.hp1 HG01891.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1597-421G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767958 | ||||||
chr16:767959
|
T | C | 1 | a0014c0047t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-420T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767959 | ||||||
chr16:767961
|
G | GGGGGGCG others(83): Show |
1 | a0002c0003t0004g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1597-418_1597-417i others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767961 | ||||||
chr16:767961
|
G | GGGGGGTG others(40): Show |
2 | a0007c0012t0001g0246a0013c0019t0001g0006 | 4 | HG02451.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-418_1597-417i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767961 | ||||||
chr16:767961
|
GA | G | 4 | a0001c0001t0001g0107a0002c0003t0002g0247a0002c0003t0002g0249others(1): Show | 4 | HG01257.hp1 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-417delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767961 | ||||||
chr16:767962
|
A | AG | 14 | a0001c0001t0001g0163a0001c0001t0001g0176a0001c0001t0001g0351others(11): Show | 14 | HG01169.hp1 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1597-412dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | |||||
chr16:767962
|
A | AGGGGGGC others(15): Show |
1 | a0002c0002t0002g0337 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1597-412_1597-411i others(24): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | |||||
chr16:767962
|
A | AGGGGGGG others(40): Show |
1 | a0002c0002t0002g0344 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1597-412_1597-411i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | |||||
chr16:767962
|
A | AGGGGGGG others(49): Show |
1 | a0010c0013t0007g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1597-412_1597-411i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | |||||
chr16:767962
|
A | G | 15 | a0002c0002t0002g0313a0002c0003t0004g0213a0002c0003t0004g0234others(12): Show | 21 | HG00639.hp1 HG01891.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1597-417A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767962 | ||||||
chr16:767964
|
G | GAGGA | 10 | a0001c0001t0001g0076a0002c0003t0004g0211a0008c0009t0002g0044others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-415_1597-414i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767964 | ||||||
chr16:767966
|
G | C | 5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-413G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767966 | ||||||
chr16:767967
|
G | T | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0026others(2): Show | 5 | HG02451.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-412G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767967 | ||||||
chr16:767968
|
C | CG | 7 | a0002c0002t0002g0313a0002c0003t0004g0212a0002c0003t0004g0220others(4): Show | 7 | HG01978.hp1 HG02004.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-411_1597-410i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | ||||||
chr16:767968
|
C | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0076others(108): Show | 129 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.1597-411C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | ||||||
chr16:767968
|
C | T | 5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-411C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | ||||||
chr16:767968
|
CCGTGTGG others(46): Show |
C | 2 | a0007c0016t0005g0012a0007c0016t0005g0229 | 3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1597-410_1597-358d others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | ||||||
chr16:767969
|
C | A | 8 | a0001c0022t0001g0270a0002c0003t0002g0260a0002c0003t0004g0215others(5): Show | 9 | HG01361.hp1 HG01934.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-410C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767969 | ||||||
chr16:767969
|
C | CGCGTGGG others(27): Show |
1 | a0002c0002t0002g0333 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1597-409_1597-408i others(36): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767969 | |||||
chr16:767969
|
C | G | 6 | a0002c0003t0004g0213a0002c0015t0003g0066a0002c0015t0003g0174others(3): Show | 10 | HG00639.hp1 HG01891.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1597-410C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767969 | ||||||
chr16:767969
|
C | T | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0026others(2): Show | 5 | HG02451.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-410C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767969 | ||||||
chr16:767970
|
G | T | 1 | a0002c0003t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1597-409G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767970 | ||||||
chr16:767971
|
T | A | 10 | a0002c0003t0004g0216a0002c0015t0003g0066a0002c0015t0003g0174others(7): Show | 14 | HG00639.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1597-408T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767971 | ||||||
chr16:767971
|
T | C | 104 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0076others(101): Show | 122 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1597-408T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767971 | ||||||
chr16:767971
|
T | G | 6 | a0002c0003t0004g0213a0006c0007t0001g0008a0006c0007t0001g0023others(3): Show | 6 | HG01943.hp2 HG02451.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-408T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767971 | ||||||
chr16:767972
|
G | A | 22 | a0001c0001t0001g0076a0002c0003t0002g0247a0002c0003t0002g0249others(19): Show | 24 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1597-407G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | ||||||
chr16:767972
|
G | GGA | 5 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-407_1597-406i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | ||||||
chr16:767972
|
G | GGGGGGGC others(3): Show |
4 | a0002c0003t0004g0230a0002c0003t0004g0231a0002c0003t0004g0232others(1): Show | 4 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-407_1597-406i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | ||||||
chr16:767972
|
G | GGGGGGGC others(4): Show |
1 | a0002c0003t0004g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1597-407_1597-406i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | ||||||
chr16:767972
|
G | GGGGGGGC others(98): Show |
1 | a0002c0003t0004g0217 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1597-407_1597-406i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | ||||||
chr16:767972
|
G | GTGGGGGG others(6): Show |
2 | a0001c0001t0001g0252a0001c0041t0001g0152 | 2 | HG00738.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1597-399_1597-398i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767972 | |||||
chr16:767972
|
G | GTGGGGGG others(369): Show |
1 | a0002c0003t0004g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1597-399_1597-398i others(378): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767972 | |||||
chr16:767972
|
GT | G | 5 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(2): Show | 9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-406delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | ||||||
chr16:767973
|
T | A | 2 | a0002c0002t0002g0313a0002c0003t0004g0213 | 2 | HG01943.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-406T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767973 | ||||||
chr16:767973
|
T | G | 12 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(9): Show | 12 | HG01978.hp1 HG02004.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1597-406T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767973 | ||||||
chr16:767973
|
T | TGGAGGGG others(62): Show |
1 | a0014c0047t0003g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-404_1597-403i others(71): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767973
|
T | TGGAGGGG others(32): Show |
1 | a0003c0004t0003g0227 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1597-404_1597-403i others(41): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767973
|
T | TGGAGGGG others(33): Show |
3 | a0003c0004t0003g0226a0003c0004t0003g0273a0003c0004t0003g0291 | 3 | HG02486.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1597-404_1597-403i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767973
|
T | TGGAGGGG others(49): Show |
1 | a0010c0013t0007g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1597-404_1597-403i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767973
|
T | TGGAGGGG others(50): Show |
2 | a0010c0013t0006g0209a0010c0013t0006g0210 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1597-404_1597-403i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767973
|
T | TGGGAGGG others(75): Show |
1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1597-403_1597-402i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767973
|
TG | T | 8 | a0001c0001t0001g0075a0002c0002t0002g0307a0003c0004t0003g0274others(5): Show | 9 | HG00733.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-399delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | |||||
chr16:767979
|
G | C | 20 | a0002c0015t0003g0066a0002c0015t0003g0174a0003c0004t0003g0002others(17): Show | 24 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597-400G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767979 | ||||||
chr16:767979
|
G | GCGTGGAG others(112): Show |
1 | a0003c0004t0003g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1597-400_1597-399i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767979 | ||||||
chr16:767979
|
G | GGCGTGGA others(8): Show |
1 | a0001c0001t0001g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | |||||
chr16:767979
|
G | GGGCGCAT others(20): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0341a0016c0029t0001g0225 | 3 | HG00597.hp2 HG01884.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1597-399_1597-398i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | |||||
chr16:767979
|
G | GGT | 7 | a0001c0001t0001g0222a0002c0002t0002g0289a0002c0002t0002g0334others(4): Show | 9 | HG00621.hp1 HG01109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-399_1597-398i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | |||||
chr16:767979
|
G | GGTGTGGA others(41): Show |
1 | a0002c0003t0002g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1597-399_1597-398i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | |||||
chr16:767979
|
G | T | 8 | a0001c0001t0001g0223a0001c0001t0001g0348a0001c0001t0001g0349others(5): Show | 10 | HG01952.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-400G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767979 | ||||||
chr16:767980
|
G | C | 1 | a0027c0026t0001g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1597-399G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767980 | ||||||
chr16:767981
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0076others(58): Show | 74 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1597-398C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767981 | ||||||
chr16:767982
|
G | A | 5 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0237others(2): Show | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-397G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767982 | ||||||
chr16:767985
|
G | T | 1 | a0002c0002t0002g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1597-394G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767985 | ||||||
chr16:767986
|
A | AGGGGGGC others(42): Show |
3 | a0002c0002t0002g0314a0002c0002t0002g0316a0002c0002t0002g0336 | 3 | HG00099.hp2 NA18970.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1597-384_1597-383i others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767986 | |||||
chr16:767986
|
A | AGGGGGGC others(43): Show |
1 | a0002c0002t0012g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1597-384_1597-383i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767986 | |||||
chr16:767986
|
A | AGTGGGGT others(8): Show |
1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1597-392_1597-391i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767986 | |||||
chr16:767986
|
A | G | 2 | a0001c0022t0001g0178a0002c0002t0002g0313 | 2 | HG03669.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-393A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767986 | ||||||
chr16:767987
|
G | GGGGGGCG others(104): Show |
1 | a0001c0001t0001g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1597-332_1597-331i others(113): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767987 | |||||
chr16:767987
|
G | GGGGGGCG others(227): Show |
2 | a0006c0007t0001g0014a0006c0007t0001g0258 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1597-380_1597-379i others(236): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767987 | |||||
chr16:767987
|
G | GGGGGGCG others(1265): Show |
1 | a0006c0007t0001g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1597-380_1597-379i others(1274): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767987 | |||||
chr16:767988
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1597-391G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GA | 49 | a0001c0001t0001g0134a0001c0001t0001g0222a0001c0001t0001g0223others(46): Show | 56 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1597-391_1597-390i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(103): Show |
2 | a0003c0004t0003g0019a0003c0004t0003g0352 | 3 | HG01884.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1597-391_1597-390i others(112): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(117): Show |
6 | a0003c0004t0003g0015a0003c0004t0003g0016a0003c0004t0003g0272others(3): Show | 7 | HG01106.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-391_1597-390i others(126): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(118): Show |
2 | a0002c0015t0003g0255a0002c0015t0003g0256 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1597-391_1597-390i others(127): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(119): Show |
1 | a0003c0004t0003g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(128): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(120): Show |
1 | a0002c0034t0003g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(129): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(246): Show |
1 | a0005c0005t0001g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(255): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(91): Show |
1 | a0002c0003t0002g0248 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(115): Show |
1 | a0002c0003t0002g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(116): Show |
1 | a0002c0003t0004g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(125): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(75): Show |
1 | a0004c0006t0001g0346 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(90): Show |
11 | a0004c0006t0001g0181a0004c0006t0001g0224a0004c0006t0001g0251others(8): Show | 11 | HG00558.hp1 HG02071.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1597-391_1597-390i others(99): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(90): Show |
3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244 | 3 | HG02717.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1597-391_1597-390i others(99): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(91): Show |
1 | a0004c0021t0001g0345 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(128): Show |
1 | a0004c0006t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(137): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GAGGGGCG others(92): Show |
1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(101): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | ||||||
chr16:767988
|
G | GGGCACGT others(99): Show |
1 | a0001c0022t0001g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1597-389_1597-388i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCAC others(44): Show |
1 | a0002c0002t0002g0338 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1597-386_1597-385i others(53): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCAC others(43): Show |
2 | a0002c0002t0002g0308a0002c0002t0002g0312 | 2 | HG03942.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1597-386_1597-385i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCAC others(42): Show |
33 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0017others(30): Show | 44 | HG00733.hp2 HG01069.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1597-386_1597-385i others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCAC others(43): Show |
2 | a0002c0002t0002g0294a0002c0002t0002g0311 | 2 | HG02080.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1597-386_1597-385i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(216): Show |
1 | a0009c0031t0002g0353 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1597-384_1597-383i others(225): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(8): Show |
1 | a0003c0004t0003g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1597-388_1597-374d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(154): Show |
1 | a0001c0001t0001g0286 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1597-335_1597-334i others(163): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(122): Show |
1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1597-332_1597-331i others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(127): Show |
1 | a0001c0001t0001g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(136): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(112): Show |
1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGCGC others(89): Show |
1 | a0001c0001t0001g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1597-377_1597-376i others(98): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGGCA others(43): Show |
1 | a0002c0002t0002g0328 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1597-387_1597-386i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGGCG others(61): Show |
1 | a0017c0023t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1597-387_1597-386i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767988
|
G | GGGGGTGC others(8): Show |
10 | a0001c0041t0001g0152a0002c0003t0004g0212a0002c0003t0004g0214others(7): Show | 10 | HG01978.hp1 HG02004.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-387_1597-386i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | |||||
chr16:767993
|
C | T | 1 | a0008c0009t0002g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-386C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767993 | ||||||
chr16:767994
|
G | A | 1 | a0002c0002t0002g0317 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-385G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767994 | ||||||
chr16:767995
|
C | A | 2 | a0002c0003t0004g0218a0002c0003t0004g0219 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1597-384C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767995 | ||||||
chr16:767996
|
G | A | 1 | a0002c0002t0002g0317 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-383G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767996 | ||||||
chr16:767997
|
TGGAGGAG others(24): Show |
T | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-379_1597-349d others(33): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767997 | |||||
chr16:768000
|
A | AGGAGGAG others(45): Show |
1 | a0005c0005t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1597-329_1597-328i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | |||||
chr16:768000
|
A | AGGGGGGC others(41): Show |
2 | a0002c0003t0004g0218a0002c0003t0004g0219 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1597-377_1597-376i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | |||||
chr16:768000
|
A | AGGGGGGG others(5): Show |
1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-377_1597-376i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | |||||
chr16:768000
|
A | AGGGGGGG others(17): Show |
2 | a0007c0012t0001g0004a0007c0012t0001g0245 | 4 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-377_1597-376i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | |||||
chr16:768000
|
A | G | 10 | a0002c0002t0002g0317a0002c0003t0004g0211a0008c0009t0002g0044others(7): Show | 10 | HG01516.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1597-379A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768000 | ||||||
chr16:768001
|
G | GGGGGCGC | 8 | a0002c0003t0004g0211a0008c0009t0002g0044a0008c0009t0002g0045others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1597-377_1597-376i others(9): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768001 | |||||
chr16:768003
|
A | AGGGGCGC others(57): Show |
1 | a0008c0009t0002g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768003 | |||||
chr16:768003
|
A | G | 2 | a0001c0022t0001g0270a0014c0024t0002g0029 | 2 | HG01361.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1597-376A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768003 | ||||||
chr16:768003
|
A | T | 9 | a0002c0002t0002g0317a0002c0003t0004g0211a0008c0009t0002g0044others(6): Show | 9 | HG01516.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1597-376A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768003 | ||||||
chr16:768006
|
A | G | 15 | a0001c0022t0001g0270a0002c0002t0002g0317a0002c0003t0004g0211others(12): Show | 15 | HG00642.hp1 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1597-373A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768006 | ||||||
chr16:768013
|
C | T | 1 | a0002c0002t0002g0317 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-366C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768013 | ||||||
chr16:768014
|
A | G | 9 | a0002c0002t0002g0049a0002c0002t0002g0317a0004c0006t0001g0267others(6): Show | 13 | HG00642.hp1 HG01516.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-365A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768014 | ||||||
chr16:768015
|
T | G | 1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-364T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768015 | ||||||
chr16:768015
|
T | TGGGGGGG others(49): Show |
1 | a0002c0002t0002g0318 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1597-319_1597-318i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768015 | |||||
chr16:768021
|
G | C | 7 | a0004c0006t0001g0185a0004c0006t0001g0267a0004c0006t0001g0350others(4): Show | 9 | HG00642.hp1 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-358G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768021 | ||||||
chr16:768023
|
T | A | 4 | a0004c0006t0001g0267a0004c0006t0001g0350a0004c0017t0001g0264others(1): Show | 4 | HG00642.hp1 HG03540.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-356T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768023 | ||||||
chr16:768023
|
T | C | 7 | a0001c0022t0001g0270a0004c0006t0001g0185a0007c0012t0001g0004others(4): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1597-356T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768023 | ||||||
chr16:768028
|
A | AG | 14 | a0001c0001t0001g0070a0001c0001t0001g0098a0001c0001t0001g0166others(11): Show | 16 | HG00639.hp2 HG01070.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1597-345dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768028 | |||||
chr16:768029
|
G | GGGGGGCG others(6): Show |
11 | a0001c0001t0001g0252a0002c0003t0002g0247a0002c0003t0002g0248others(8): Show | 13 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-334_1597-322d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768029 | |||||
chr16:768029
|
GGGGGGCG others(6): Show |
G | 17 | a0001c0001t0001g0279a0001c0022t0001g0178a0002c0002t0002g0320others(14): Show | 17 | HG00558.hp1 HG01074.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.1597-334_1597-322d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768029 | |||||
chr16:768030
|
G | A | 1 | a0001c0022t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-349G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768030 | ||||||
chr16:768030
|
GGGGGCGC others(5): Show |
G | 1 | a0004c0006t0001g0262 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-344_1597-333d others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768030 | |||||
chr16:768034
|
GC | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0241others(3): Show | 6 | HG01257.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1597-344delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768034 | ||||||
chr16:768035
|
C | T | 1 | a0001c0022t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-344C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768035 | ||||||
chr16:768036
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-343G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768036 | ||||||
chr16:768036
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G | T | 1 | a0001c0022t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-343G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768036 | ||||||
chr16:768037
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C | CGTGGAGG others(113): Show |
1 | a0017c0023t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1597-331_1597-330i others(122): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768037 | |||||
chr16:768037
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C | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG01257.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-342C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768037 | ||||||
chr16:768040
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G | GGGGGGGG others(76): Show |
1 | a0004c0017t0001g0264 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1597-338_1597-337i others(85): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768040 | |||||
chr16:768041
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G | GGGGGGGC others(75): Show |
2 | a0004c0006t0001g0267a0004c0006t0001g0350 | 2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1597-338_1597-337i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768041 | ||||||
chr16:768041
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G | GGGGGGGT others(147): Show |
1 | a0002c0002t0002g0330 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1597-338_1597-337i others(156): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768041 | ||||||
chr16:768042
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A | AG | 9 | a0001c0001t0001g0061a0001c0001t0001g0149a0001c0001t0001g0157others(6): Show | 9 | HG00408.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-332dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGAGGAG others(23): Show |
1 | a0002c0002t0002g0317 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-335_1597-334i others(32): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGAGGGG others(37): Show |
1 | a0001c0022t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-335_1597-334i others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGCA others(127): Show |
1 | a0027c0026t0001g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1597-331_1597-330i others(136): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGCA others(150): Show |
4 | a0002c0002t0002g0314a0002c0002t0002g0316a0002c0002t0002g0336others(1): Show | 4 | HG00099.hp2 HG02004.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-331_1597-330i others(159): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGCC others(157): Show |
1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-331_1597-330i others(166): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGCG others(7): Show |
1 | a0006c0007t0001g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1597-335_1597-322d others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGGG others(22): Show |
2 | a0007c0012t0001g0004a0007c0012t0001g0245 | 4 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-332_1597-331i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGGG others(37): Show |
1 | a0013c0019t0001g0006 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1597-332_1597-331i others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | AGGGGGGG others(104): Show |
1 | a0004c0006t0001g0346 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597-332_1597-331i others(113): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | |||||
chr16:768042
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A | G | 5 | a0002c0002t0002g0330a0004c0006t0001g0267a0004c0006t0001g0350others(2): Show | 5 | HG00642.hp1 HG03540.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-337A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768042 | ||||||
chr16:768044
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G | A | 2 | a0002c0002t0002g0017a0002c0002t0002g0337 | 3 | NA18943.hp1 NA18945.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1597-335G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768044 | ||||||
chr16:768048
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C | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0073a0009c0011t0001g0005 | 4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-331C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768048 | ||||||
chr16:768051
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G | A | 1 | a0005c0005t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1597-328G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768051 | ||||||
chr16:768051
|
GTGGAGGA others(8): Show |
G | 3 | a0012c0018t0001g0078a0012c0018t0001g0079a0012c0018t0001g0186 | 3 | HG01123.hp1 HG01256.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1597-321_1597-307d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768051 | |||||
chr16:768073
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G | C | 4 | a0006c0010t0001g0013a0006c0010t0001g0236a0006c0010t0001g0238others(1): Show | 5 | HG01981.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-306G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768073 | ||||||
chr16:768077
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G | T | 7 | a0002c0003t0004g0218a0002c0003t0004g0219a0002c0003t0004g0230others(4): Show | 7 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-302G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768077 | ||||||
chr16:768090
|
GC | G | 3 | a0001c0001t0001g0149a0002c0002t0002g0307a0027c0026t0001g0169 | 3 | HG00408.hp1 HG01175.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1597-286delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768090 | |||||
chr16:768114
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G | T | 1 | a0002c0025t0002g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1597-265G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768114 | ||||||
chr16:768118
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G | T | 24 | a0001c0001t0011g0202a0002c0015t0003g0066a0002c0015t0003g0174others(21): Show | 30 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1597-261G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768118 | ||||||
chr16:768153
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C | G | 1 | a0004c0006t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-226C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768153 | ||||||
chr16:768173
|
AGGAAGGG others(28): Show |
A | 1 | a0003c0004t0003g0276 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1597-194_1597-160d others(37): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768173 | |||||
chr16:768193
|
G | A | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1597-186G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768193 | ||||||
chr16:768212
|
AGGGCAGC others(8): Show |
A | 1 | a0002c0002t0002g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1597-166_1597-152d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768212 | ||||||
chr16:768242
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1597-137C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768242 | ||||||
chr16:768253
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1597-126G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768253 | ||||||
chr16:768294
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G | A | 1 | a0002c0034t0003g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1597-85G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768294 | ||||||
chr16:768325
|
G | T | 2 | a0001c0022t0001g0270a0004c0006t0001g0240 | 2 | HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1597-54G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768325 | ||||||
chr16:768353
|
TGATGGCT others(5): Show |
T | 1 | a0015c0020t0002g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1597-24_1597-13del others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768353 | |||||
chr16:768582
|
G | A | 1 | a0002c0003t0004g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1783+17G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/17 | chr16 | 768582 | ||||||
chr16:768643
|
T | C | 29 | a0002c0003t0002g0268a0002c0015t0003g0066a0002c0015t0003g0174others(26): Show | 35 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.1784-5T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/17 | chr16 | 768643 |