geneid | 114803 |
---|---|
ensemblid | ENSG00000162601.12 |
hgncid | 29401 |
symbol | MYSM1 |
name | Myb like, SWIRM and MPN domains 1 |
refseq_nuc | NM_001085487.3 |
refseq_prot | NP_001078956.1 |
ensembl_nuc | ENST00000472487.6 |
ensembl_prot | ENSP00000418734.1 |
mane_status | MANE Select |
chr | chr1 |
start | 58654743 |
end | 58700062 |
strand | - |
ver | v1.2 |
region | chr1:58654743-58700062 |
region5000 | chr1:58649743-58705062 |
regionname0 | MYSM1_chr1_58654743_58700062 |
regionname5000 | MYSM1_chr1_58649743_58705062 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 828 | 139 | 21 | 24 | 75 | 5 | 14 | 60 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002 | 1/1 | 828 | 137 | 23 | 19 | 75 | 6 | 12 | 63 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003 | 0/0 | 828 | 59 | 0 | 7 | 42 | 1 | 9 | 28 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004 | 0/0 | 828 | 58 | 39 | 15 | 0 | 0 | 4 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005 | 0/0 | 828 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0006 | 0/0 | 828 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0007 | 0/0 | 828 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0008 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0009 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0010 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2487 | 139 | 21 | 24 | 75 | 5 | 14 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0002 | 0/1 | 2487 | 97 | 11 | 14 | 58 | 3 | 10 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0003 | 0/0 | 2487 | 59 | 0 | 7 | 42 | 1 | 9 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0004 | 0/0 | 2487 | 58 | 39 | 15 | 0 | 0 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0005 | 1/0 | 2487 | 40 | 12 | 5 | 17 | 3 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0006 | 0/0 | 2487 | 6 | 6 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0007 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0008 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0009 | 0/0 | 2487 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0010 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0011 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0012 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
c0013 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5273 | 58 | 8 | 3 | 39 | 2 | 6 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0002 | 0/1 | 5275 | 49 | 2 | 8 | 32 | 3 | 3 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0003 | 0/0 | 5278 | 46 | 10 | 5 | 25 | 1 | 5 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0004 | 0/0 | 5275 | 27 | 3 | 9 | 9 | 2 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0005 | 0/0 | 5277 | 20 | 1 | 4 | 13 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0006 | 1/0 | 5265 | 17 | 3 | 1 | 9 | 1 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0007 | 0/0 | 5280 | 12 | 1 | 4 | 3 | 0 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0008 | 0/0 | 5277 | 11 | 0 | 7 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0009 | 0/0 | 5271 | 11 | 3 | 0 | 7 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0010 | 0/0 | 5276 | 9 | 4 | 1 | 2 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0011 | 0/0 | 5274 | 7 | 4 | 0 | 2 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0012 | 0/0 | 5272 | 6 | 4 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0013 | 0/0 | 5271 | 6 | 1 | 1 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0014 | 0/0 | 5279 | 5 | 0 | 1 | 3 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0015 | 0/0 | 5292 | 5 | 0 | 0 | 5 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0016 | 0/0 | 5261 | 5 | 1 | 2 | 0 | 2 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0017 | 0/0 | 5279 | 4 | 0 | 3 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0018 | 0/0 | 5267 | 4 | 0 | 0 | 2 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0019 | 0/0 | 5274 | 4 | 0 | 0 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0020 | 0/0 | 5275 | 4 | 4 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0021 | 0/0 | 5269 | 3 | 0 | 0 | 2 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0022 | 0/0 | 5282 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0023 | 0/0 | 5277 | 3 | 2 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0024 | 0/0 | 5267 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0025 | 0/0 | 5273 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0026 | 0/0 | 5272 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0027 | 0/0 | 5272 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0028 | 0/0 | 5271 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0029 | 0/0 | 5268 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0030 | 0/0 | 5267 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0031 | 0/0 | 5271 | 3 | 1 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0032 | 0/0 | 5271 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0033 | 0/0 | 5274 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0034 | 0/0 | 5263 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0035 | 0/0 | 5276 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0036 | 0/0 | 5269 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0037 | 0/0 | 5269 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0038 | 0/0 | 5278 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0039 | 0/0 | 5278 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0040 | 0/0 | 5273 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0041 | 0/0 | 5275 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0042 | 0/0 | 5273 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0043 | 0/0 | 5270 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0044 | 0/0 | 5267 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0045 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0046 | 0/0 | 5276 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0047 | 0/0 | 5283 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0048 | 0/0 | 5274 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0049 | 0/0 | 5273 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0050 | 0/0 | 5270 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0051 | 0/0 | 5259 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0052 | 0/0 | 5253 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0053 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0054 | 0/0 | 5273 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0055 | 0/0 | 5273 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0056 | 0/0 | 5272 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0057 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0058 | 0/0 | 5276 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0059 | 0/0 | 5276 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0060 | 0/0 | 5278 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0061 | 0/0 | 5279 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0062 | 0/0 | 5282 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0063 | 0/0 | 5280 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0064 | 0/0 | 5279 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0065 | 0/0 | 5278 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0066 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0067 | 0/0 | 5274 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0068 | 0/0 | 5274 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0069 | 0/0 | 5274 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0070 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0071 | 0/0 | 5263 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0072 | 0/0 | 5272 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0073 | 0/0 | 5283 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0074 | 0/0 | 5279 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0075 | 0/0 | 5273 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0076 | 0/0 | 5269 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0077 | 0/0 | 5263 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0078 | 0/0 | 5267 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0079 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0080 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0081 | 0/0 | 5277 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0082 | 0/0 | 5278 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
t0083 | 0/0 | 5275 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0002 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0340 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2487 | 139 | 21 | 24 | 75 | 5 | 14 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002 | 0/1 | 2487 | 97 | 11 | 14 | 58 | 3 | 10 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005 | 1/0 | 2487 | 40 | 12 | 5 | 17 | 3 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003 | 0/0 | 2487 | 59 | 0 | 7 | 42 | 1 | 9 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004 | 0/0 | 2487 | 58 | 39 | 15 | 0 | 0 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005c0006 | 0/0 | 2487 | 6 | 6 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005c0008 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0006c0007 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0006c0010 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0007c0009 | 0/0 | 2487 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0008c0013 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0009c0012 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0010c0011 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7759 | 56 | 8 | 2 | 39 | 2 | 5 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0004 | 0/0 | 7761 | 27 | 3 | 9 | 9 | 2 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0008 | 0/0 | 7763 | 11 | 0 | 7 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0009 | 0/0 | 7757 | 11 | 3 | 0 | 7 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0017 | 0/0 | 7765 | 4 | 0 | 3 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0018 | 0/0 | 7753 | 4 | 0 | 0 | 2 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0019 | 0/0 | 7760 | 4 | 0 | 0 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0021 | 0/0 | 7755 | 3 | 0 | 0 | 2 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0033 | 0/0 | 7760 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0034 | 0/0 | 7749 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0036 | 0/0 | 7755 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0037 | 0/0 | 7755 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0046 | 0/0 | 7762 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0047 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0049 | 0/0 | 7759 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0050 | 0/0 | 7756 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0051 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0052 | 0/0 | 7739 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0053 | 0/0 | 7757 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0054 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0055 | 0/0 | 7759 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0056 | 0/0 | 7758 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0001c0001t0057 | 0/0 | 7751 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0002 | 0/1 | 7761 | 49 | 2 | 8 | 32 | 3 | 3 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0005 | 0/0 | 7763 | 19 | 1 | 4 | 12 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0013 | 0/0 | 7757 | 6 | 1 | 1 | 4 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0014 | 0/0 | 7765 | 5 | 0 | 1 | 3 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0028 | 0/0 | 7757 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0041 | 0/0 | 7761 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0042 | 0/0 | 7759 | 2 | 0 | 0 | 1 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0044 | 0/0 | 7753 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0045 | 0/0 | 7751 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0073 | 0/0 | 7769 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0074 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0075 | 0/0 | 7759 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0076 | 0/0 | 7755 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0077 | 0/0 | 7749 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0078 | 0/0 | 7753 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0002t0083 | 0/0 | 7761 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0006 | 1/0 | 7751 | 17 | 3 | 1 | 9 | 1 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0015 | 0/0 | 7778 | 5 | 0 | 0 | 5 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0016 | 0/0 | 7747 | 5 | 1 | 2 | 0 | 2 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0027 | 0/0 | 7758 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0029 | 0/0 | 7754 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0030 | 0/0 | 7753 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0043 | 0/0 | 7756 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0079 | 0/0 | 7747 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0002c0005t0080 | 0/0 | 7747 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0003 | 0/0 | 7764 | 33 | 0 | 2 | 25 | 1 | 5 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0007 | 0/0 | 7766 | 4 | 0 | 1 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0010 | 0/0 | 7762 | 5 | 0 | 1 | 2 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0011 | 0/0 | 7760 | 3 | 0 | 0 | 2 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0022 | 0/0 | 7768 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0035 | 0/0 | 7762 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0038 | 0/0 | 7764 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0058 | 0/0 | 7762 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0059 | 0/0 | 7762 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0062 | 0/0 | 7768 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0064 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0065 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0067 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0003c0003t0082 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0003 | 0/0 | 7764 | 11 | 8 | 3 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0007 | 0/0 | 7766 | 8 | 1 | 3 | 0 | 0 | 4 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0010 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0012 | 0/0 | 7758 | 6 | 4 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0020 | 0/0 | 7761 | 4 | 4 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0023 | 0/0 | 7763 | 3 | 2 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0024 | 0/0 | 7753 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0026 | 0/0 | 7758 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0031 | 0/0 | 7757 | 3 | 1 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0032 | 0/0 | 7757 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0039 | 0/0 | 7764 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0040 | 0/0 | 7759 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0060 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0061 | 0/0 | 7765 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0063 | 0/0 | 7766 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0066 | 0/0 | 7751 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0068 | 0/0 | 7760 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0069 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0070 | 0/0 | 7757 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0071 | 0/0 | 7749 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0072 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0004c0004t0081 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005c0006t0003 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005c0006t0011 | 0/0 | 7760 | 4 | 4 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005c0006t0026 | 0/0 | 7758 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0005c0008t0010 | 0/0 | 7762 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0006c0007t0025 | 0/0 | 7759 | 3 | 3 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0006c0010t0010 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0007c0009t0001 | 0/0 | 7759 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0008c0013t0005 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0009c0012t0048 | 0/0 | 7760 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
a0010c0011t0003 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | copy fasta | chr1 | 58649743 | 58705062 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0002 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0009g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0017g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0017g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0017g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0018g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0018g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0018g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0019g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0019g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0019g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0021g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0021g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0021g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0033g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0033g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0034g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0034g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0036g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0036g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0037g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0037g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0046g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0047g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0049g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0050g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0051g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0052g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0053g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0054g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0055g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0056g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0001c0001t0057g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0013g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0013g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0013g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0013g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0013g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0013g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0014g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0014g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0014g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0028g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0028g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0028g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0041g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0042g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0042g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0044g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0045g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0045g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0073g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0074g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0075g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0076g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0077g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0078g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0002t0083g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0006g0340 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0015g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0015g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0015g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0015g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0016g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0016g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0016g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0016g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0016g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0027g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0027g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0029g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0029g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0030g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0030g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0030g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0043g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0079g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0002c0005t0080g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0007g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0007g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0010g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0010g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0010g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0010g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0011g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0011g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0022g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0022g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0022g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0035g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0035g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0038g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0058g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0059g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0062g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0064g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0065g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0067g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0003c0003t0082g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0007g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0010g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0012g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0012g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0012g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0012g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0012g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0012g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0020g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0020g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0020g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0020g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0023g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0023g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0023g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0024g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0024g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0024g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0026g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0031g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0031g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0032g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0032g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0032g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0039g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0039g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0040g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0040g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0060g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0061g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0063g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0066g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0068g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0069g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0070g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0071g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0072g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0004c0004t0081g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0006t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0006t0011g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0006t0011g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0006t0011g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0006t0011g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0006t0026g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0005c0008t0010g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0006c0007t0025g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0006c0007t0025g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0006c0007t0025g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0006c0010t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0007c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0007c0009t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0008c0013t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0009c0012t0048g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
a0010c0011t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0083 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00099 | hp2 | a0001 | c0001 | t0009 | g0230 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00140 | hp2 | a0002 | c0005 | t0006 | g0256 | EUR | GBR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00280 | hp2 | a0003 | c0003 | t0003 | g0318 | EUR | FIN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00423 | hp1 | a0002 | c0002 | t0005 | g0080 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00423 | hp2 | a0001 | c0001 | t0034 | g0149 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00438 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00544 | hp1 | a0002 | c0002 | t0014 | g0130 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00544 | hp2 | a0002 | c0002 | t0005 | g0075 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00597 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00621 | hp1 | a0008 | c0013 | t0005 | g0074 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00639 | hp1 | a0002 | c0002 | t0005 | g0082 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00639 | hp2 | a0004 | c0004 | t0007 | g0335 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0115 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00673 | hp1 | a0002 | c0005 | t0006 | g0261 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00673 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00735 | hp1 | a0002 | c0002 | t0013 | g0132 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00738 | hp1 | a0004 | c0004 | t0023 | g0325 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00738 | hp2 | a0002 | c0005 | t0080 | g0248 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00741 | hp1 | a0002 | c0005 | t0016 | g0254 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0041 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01074 | hp1 | a0002 | c0005 | t0043 | g0023 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01074 | hp2 | a0004 | c0004 | t0003 | g0277 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01081 | hp1 | a0004 | c0004 | t0003 | g0283 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0155 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01099 | hp1 | a0003 | c0003 | t0010 | g0333 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0200 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01106 | hp1 | a0003 | c0003 | t0003 | g0319 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01106 | hp2 | a0002 | c0002 | t0005 | g0084 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01109 | hp2 | a0004 | c0004 | t0003 | g0349 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01167 | hp1 | a0004 | c0004 | t0012 | g0366 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01167 | hp2 | a0004 | c0004 | t0007 | g0026 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01169 | hp2 | a0004 | c0004 | t0007 | g0026 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01192 | hp1 | a0001 | c0001 | t0057 | g0042 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0218 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01243 | hp2 | a0001 | c0001 | t0037 | g0275 | AMR | PUR | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0065 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01255 | hp2 | a0004 | c0004 | t0012 | g0367 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01256 | hp1 | a0007 | c0009 | t0001 | g0227 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01256 | hp2 | a0004 | c0004 | t0031 | g0028 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01257 | hp1 | a0001 | c0001 | t0008 | g0163 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01257 | hp2 | a0003 | c0003 | t0038 | g0024 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01258 | hp1 | a0004 | c0004 | t0031 | g0028 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01258 | hp2 | a0003 | c0003 | t0038 | g0024 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01346 | hp2 | a0002 | c0002 | t0014 | g0102 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01361 | hp2 | a0001 | c0001 | t0017 | g0013 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01496 | hp2 | a0004 | c0004 | t0069 | g0364 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0225 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01515 | hp2 | a0002 | c0005 | t0016 | g0257 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0146 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0009 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0009 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01517 | hp2 | a0002 | c0005 | t0016 | g0260 | EUR | IBS | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01884 | hp1 | a0006 | c0007 | t0025 | g0047 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01884 | hp2 | a0004 | c0004 | t0072 | g0037 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01891 | hp2 | a0002 | c0002 | t0044 | g0006 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01934 | hp1 | a0001 | c0001 | t0047 | g0177 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01934 | hp2 | a0002 | c0002 | t0005 | g0099 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01952 | hp1 | a0001 | c0001 | t0008 | g0157 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01952 | hp2 | a0004 | c0004 | t0063 | g0353 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01978 | hp2 | a0001 | c0001 | t0008 | g0142 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01981 | hp1 | a0003 | c0003 | t0067 | g0298 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01993 | hp2 | a0002 | c0005 | t0016 | g0255 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02004 | hp1 | a0003 | c0003 | t0007 | g0285 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02004 | hp2 | a0004 | c0004 | t0039 | g0354 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02015 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02015 | hp2 | a0003 | c0003 | t0011 | g0299 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02040 | hp2 | a0003 | c0003 | t0058 | g0301 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02055 | hp1 | a0004 | c0004 | t0024 | g0030 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02074 | hp1 | a0003 | c0003 | t0003 | g0278 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02074 | hp2 | a0001 | c0001 | t0009 | g0137 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02080 | hp1 | a0003 | c0003 | t0022 | g0336 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02083 | hp1 | a0002 | c0002 | t0028 | g0090 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02083 | hp2 | a0003 | c0003 | t0022 | g0321 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02129 | hp1 | a0002 | c0002 | t0028 | g0089 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02132 | hp2 | a0003 | c0003 | t0022 | g0284 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02145 | hp2 | a0006 | c0007 | t0025 | g0045 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02148 | hp2 | a0001 | c0001 | t0017 | g0173 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02155 | hp1 | a0003 | c0003 | t0010 | g0297 | EAS | CDX | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02155 | hp2 | a0001 | c0001 | t0051 | g0191 | EAS | CDX | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02257 | hp1 | a0004 | c0004 | t0020 | g0347 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02257 | hp2 | a0005 | c0006 | t0003 | g0359 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0357 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02258 | hp2 | a0004 | c0004 | t0023 | g0348 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02273 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02273 | hp2 | a0004 | c0004 | t0039 | g0355 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02280 | hp1 | a0002 | c0005 | t0027 | g0021 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02280 | hp2 | a0004 | c0004 | t0020 | g0327 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02300 | hp1 | a0001 | c0001 | t0008 | g0178 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02300 | hp2 | a0002 | c0002 | t0005 | g0131 | AMR | PEL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02523 | hp1 | a0002 | c0002 | t0083 | g0073 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02523 | hp2 | a0003 | c0003 | t0003 | g0304 | EAS | KHV | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02572 | hp1 | a0005 | c0006 | t0011 | g0358 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02572 | hp2 | a0001 | c0001 | t0050 | g0202 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0303 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02602 | hp2 | a0003 | c0003 | t0003 | g0027 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02615 | hp1 | a0002 | c0005 | t0029 | g0356 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02615 | hp2 | a0004 | c0004 | t0024 | g0031 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02622 | hp1 | a0004 | c0004 | t0024 | g0032 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02622 | hp2 | a0002 | c0005 | t0006 | g0252 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02630 | hp1 | a0002 | c0002 | t0013 | g0126 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02683 | hp2 | a0003 | c0003 | t0010 | g0287 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02698 | hp1 | a0003 | c0003 | t0062 | g0291 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02698 | hp2 | a0002 | c0002 | t0073 | g0081 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02717 | hp1 | a0001 | c0001 | t0053 | g0043 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02717 | hp2 | a0005 | c0006 | t0011 | g0361 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02723 | hp1 | a0002 | c0002 | t0078 | g0040 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02723 | hp2 | a0004 | c0004 | t0081 | g0344 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02735 | hp1 | a0004 | c0004 | t0007 | g0338 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02735 | hp2 | a0002 | c0005 | t0006 | g0234 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02738 | hp1 | a0002 | c0002 | t0005 | g0105 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02738 | hp2 | a0001 | c0001 | t0018 | g0208 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02809 | hp1 | a0006 | c0010 | t0010 | g0266 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02809 | hp2 | a0004 | c0004 | t0071 | g0035 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02818 | hp1 | a0002 | c0005 | t0006 | g0249 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02818 | hp2 | a0002 | c0002 | t0005 | g0124 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02886 | hp1 | a0002 | c0002 | t0045 | g0038 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02886 | hp2 | a0004 | c0004 | t0003 | g0025 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02895 | hp1 | a0004 | c0004 | t0012 | g0370 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02895 | hp2 | a0004 | c0004 | t0003 | g0312 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02896 | hp1 | a0004 | c0004 | t0003 | g0288 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02896 | hp2 | a0005 | c0008 | t0010 | g0005 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02897 | hp1 | a0004 | c0004 | t0012 | g0369 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02897 | hp2 | a0005 | c0008 | t0010 | g0005 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02922 | hp1 | a0005 | c0006 | t0011 | g0363 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02922 | hp2 | a0002 | c0005 | t0027 | g0251 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02965 | hp1 | a0004 | c0004 | t0032 | g0339 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02965 | hp2 | a0002 | c0002 | t0076 | g0049 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02970 | hp1 | a0004 | c0004 | t0032 | g0343 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02976 | hp2 | a0002 | c0005 | t0029 | g0022 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03041 | hp1 | a0004 | c0004 | t0003 | g0331 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03041 | hp2 | a0002 | c0005 | t0043 | g0023 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03098 | hp1 | a0001 | c0001 | t0036 | g0044 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03098 | hp2 | a0004 | c0004 | t0061 | g0311 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03130 | hp1 | a0001 | c0001 | t0037 | g0273 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03130 | hp2 | a0004 | c0004 | t0060 | g0282 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03139 | hp1 | a0002 | c0005 | t0027 | g0021 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03139 | hp2 | a0002 | c0005 | t0079 | g0264 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03195 | hp1 | a0005 | c0006 | t0011 | g0360 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03195 | hp2 | a0004 | c0004 | t0003 | g0281 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03209 | hp1 | a0004 | c0004 | t0026 | g0033 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03209 | hp2 | a0006 | c0007 | t0025 | g0048 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03225 | hp1 | a0002 | c0005 | t0029 | g0022 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03225 | hp2 | a0004 | c0004 | t0026 | g0034 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03239 | hp1 | a0001 | c0001 | t0021 | g0193 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03239 | hp2 | a0002 | c0005 | t0006 | g0236 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03453 | hp1 | a0002 | c0002 | t0045 | g0039 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03453 | hp2 | a0004 | c0004 | t0007 | g0315 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03486 | hp1 | a0004 | c0004 | t0012 | g0368 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03486 | hp2 | a0004 | c0004 | t0070 | g0351 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03490 | hp1 | a0002 | c0002 | t0041 | g0010 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03490 | hp2 | a0001 | c0001 | t0049 | g0211 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03491 | hp1 | a0004 | c0004 | t0007 | g0323 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03492 | hp1 | a0004 | c0004 | t0007 | g0324 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03492 | hp2 | a0002 | c0002 | t0041 | g0010 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03516 | hp1 | a0004 | c0004 | t0003 | g0025 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03516 | hp2 | a0004 | c0004 | t0020 | g0350 | AFR | ESN | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03540 | hp2 | a0004 | c0004 | t0010 | g0313 | AFR | GWD | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03579 | hp2 | a0004 | c0004 | t0066 | g0029 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03654 | hp2 | a0001 | c0001 | t0034 | g0159 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03704 | hp2 | a0002 | c0002 | t0042 | g0120 | SAS | PJL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0140 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0199 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03927 | hp1 | a0001 | c0001 | t0018 | g0217 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03927 | hp2 | a0004 | c0004 | t0007 | g0322 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0128 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04115 | hp1 | a0003 | c0003 | t0003 | g0292 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04115 | hp2 | a0002 | c0002 | t0005 | g0117 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04184 | hp1 | a0003 | c0003 | t0010 | g0337 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | BEB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04199 | hp1 | a0007 | c0009 | t0001 | g0195 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04199 | hp2 | a0002 | c0002 | t0014 | g0111 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0222 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG04228 | hp2 | a0003 | c0003 | t0003 | g0320 | SAS | STU | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18522 | hp1 | a0004 | c0004 | t0003 | g0314 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18522 | hp2 | a0004 | c0004 | t0040 | g0352 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18612 | hp1 | a0002 | c0002 | t0005 | g0060 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18747 | hp2 | a0003 | c0003 | t0065 | g0293 | EAS | CHB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18906 | hp1 | a0010 | c0011 | t0003 | g0280 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18906 | hp2 | a0001 | c0001 | t0036 | g0036 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18940 | hp2 | a0002 | c0002 | t0013 | g0092 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18941 | hp2 | a0002 | c0002 | t0042 | g0053 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18944 | hp1 | a0002 | c0002 | t0005 | g0076 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18945 | hp2 | a0003 | c0003 | t0003 | g0296 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18946 | hp1 | a0002 | c0002 | t0074 | g0057 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18946 | hp2 | a0002 | c0005 | t0006 | g0253 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18947 | hp1 | a0002 | c0002 | t0005 | g0085 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18947 | hp2 | a0003 | c0003 | t0059 | g0302 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18948 | hp1 | a0003 | c0003 | t0003 | g0306 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18948 | hp2 | a0002 | c0002 | t0014 | g0059 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18949 | hp1 | a0002 | c0005 | t0030 | g0258 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18950 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18952 | hp2 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18953 | hp1 | a0003 | c0003 | t0003 | g0307 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18953 | hp2 | a0001 | c0001 | t0019 | g0269 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18954 | hp1 | a0001 | c0001 | t0019 | g0270 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18954 | hp2 | a0002 | c0005 | t0006 | g0245 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18957 | hp2 | a0002 | c0005 | t0030 | g0250 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18960 | hp1 | a0002 | c0005 | t0015 | g0241 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18960 | hp2 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18961 | hp2 | a0003 | c0003 | t0007 | g0295 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18962 | hp1 | a0002 | c0002 | t0014 | g0054 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18962 | hp2 | a0001 | c0001 | t0052 | g0144 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18965 | hp1 | a0002 | c0005 | t0006 | g0242 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18965 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18968 | hp2 | a0002 | c0005 | t0006 | g0240 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18969 | hp1 | a0002 | c0002 | t0005 | g0050 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18970 | hp2 | a0002 | c0005 | t0006 | g0235 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18974 | hp1 | a0002 | c0005 | t0006 | g0262 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18974 | hp2 | a0009 | c0012 | t0048 | g0168 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18978 | hp2 | a0003 | c0003 | t0003 | g0305 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18979 | hp1 | a0001 | c0001 | t0046 | g0212 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18981 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18983 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18983 | hp2 | a0001 | c0001 | t0018 | g0169 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18984 | hp1 | a0001 | c0001 | t0021 | g0182 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18985 | hp1 | a0002 | c0005 | t0015 | g0243 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18985 | hp2 | a0001 | c0001 | t0056 | g0267 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18986 | hp1 | a0003 | c0003 | t0003 | g0330 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18987 | hp1 | a0002 | c0005 | t0006 | g0263 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18987 | hp2 | a0002 | c0002 | t0075 | g0095 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18990 | hp2 | a0001 | c0001 | t0019 | g0271 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18991 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18993 | hp2 | a0002 | c0005 | t0006 | g0246 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18994 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18995 | hp1 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18998 | hp1 | a0002 | c0005 | t0015 | g0244 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18998 | hp2 | a0003 | c0003 | t0003 | g0294 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA18999 | hp2 | a0002 | c0005 | t0015 | g0239 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19000 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19002 | hp1 | a0002 | c0002 | t0013 | g0118 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19002 | hp2 | a0003 | c0003 | t0003 | g0290 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19004 | hp1 | a0003 | c0003 | t0082 | g0279 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19005 | hp1 | a0002 | c0002 | t0005 | g0116 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19005 | hp2 | a0002 | c0002 | t0005 | g0067 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19009 | hp1 | a0001 | c0001 | t0009 | g0215 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19009 | hp2 | a0003 | c0003 | t0007 | g0289 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19011 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19030 | hp1 | a0004 | c0004 | t0068 | g0316 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19030 | hp2 | a0001 | c0001 | t0054 | g0326 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19043 | hp1 | a0001 | c0001 | t0055 | g0274 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19043 | hp2 | a0002 | c0002 | t0044 | g0006 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19054 | hp1 | a0001 | c0001 | t0021 | g0172 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19055 | hp1 | a0003 | c0003 | t0003 | g0135 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19055 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19057 | hp1 | a0001 | c0001 | t0009 | g0165 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19057 | hp2 | a0003 | c0003 | t0011 | g0329 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19058 | hp2 | a0002 | c0002 | t0013 | g0108 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19059 | hp1 | a0003 | c0003 | t0010 | g0310 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19060 | hp1 | a0002 | c0002 | t0005 | g0072 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19060 | hp2 | a0001 | c0001 | t0019 | g0268 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19062 | hp2 | a0002 | c0002 | t0005 | g0007 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19065 | hp1 | a0003 | c0003 | t0003 | g0300 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19070 | hp1 | a0001 | c0001 | t0033 | g0152 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19070 | hp2 | a0001 | c0001 | t0033 | g0187 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19072 | hp1 | a0002 | c0005 | t0015 | g0247 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19072 | hp2 | a0003 | c0003 | t0003 | g0328 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19075 | hp2 | a0002 | c0005 | t0030 | g0238 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19076 | hp2 | a0003 | c0003 | t0064 | g0286 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19077 | hp1 | a0002 | c0002 | t0028 | g0113 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19078 | hp1 | a0002 | c0002 | t0013 | g0121 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0181 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19080 | hp2 | a0002 | c0002 | t0005 | g0068 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19082 | hp1 | a0001 | c0001 | t0017 | g0139 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19084 | hp1 | a0001 | c0001 | t0018 | g0186 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19084 | hp2 | a0003 | c0003 | t0035 | g0332 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19085 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19087 | hp2 | a0003 | c0003 | t0007 | g0308 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19088 | hp2 | a0003 | c0003 | t0035 | g0334 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19089 | hp2 | a0003 | c0003 | t0003 | g0276 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA19240 | hp2 | a0004 | c0004 | t0040 | g0345 | AFR | YRI | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA20129 | hp1 | a0004 | c0004 | t0032 | g0342 | AFR | ASW | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA20129 | hp2 | a0004 | c0004 | t0023 | g0272 | AFR | ASW | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA20905 | hp2 | a0003 | c0003 | t0011 | g0309 | SAS | GIH | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01123 | hp1 | a0001 | c0001 | t0017 | g0013 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG01123 | hp2 | a0002 | c0005 | t0006 | g0237 | AMR | CLM | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02109 | hp2 | a0004 | c0004 | t0020 | g0346 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02486 | hp2 | a0005 | c0006 | t0026 | g0362 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02559 | hp1 | a0002 | c0005 | t0016 | g0259 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG02559 | hp2 | a0004 | c0004 | t0031 | g0341 | AFR | ACB | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | MSL | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0185 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
HG06807 | hp2 | a0002 | c0002 | t0077 | g0046 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA20300 | hp1 | a0004 | c0004 | t0003 | g0317 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | USA | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA21309 | hp1 | a0004 | c0004 | t0012 | g0365 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
NA21309 | hp2 | a0002 | c0005 | t0006 | g0265 | AFR | LWK | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0086 | REF | REF | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
homoSapiens_grch38 | hp1 | a0002 | c0005 | t0006 | g0340 | REF | REF | MYSM1_chr1_58649743_58705062 | MYSM1 | chr1 | 58649743 | 58705062 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58660011
|
C | T | 5 | a0003a0004a0005others(2): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
missense_variant | MODERATE | c.2473G>A | p.Glu825Lys | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2483/7751 | 2473/2487 | 825/828 | chr1 | 58660011 | ||
chr1:58660057
|
A | T | 1 | a0009 | 1 | NA18974.hp2 | stop_gained | HIGH | c.2427T>A | p.Tyr809* | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2437/7751 | 2427/2487 | 809/828 | chr1 | 58660057 | ||
chr1:58660058
|
T | A | 1 | a0009 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.2426A>T | p.Tyr809Phe | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2436/7751 | 2426/2487 | 809/828 | chr1 | 58660058 | ||
chr1:58660059
|
A | T | 1 | a0009 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.2425T>A | p.Tyr809Asn | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2435/7751 | 2425/2487 | 809/828 | chr1 | 58660059 | ||
chr1:58671925
|
C | G | 1 | a0010 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1606G>C | p.Glu536Gln | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/20 | 1616/7751 | 1606/2487 | 536/828 | chr1 | 58671925 | ||
chr1:58682127
|
T | G | 1 | a0005 | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
missense_variant | MODERATE | c.917A>C | p.Lys306Thr | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 927/7751 | 917/2487 | 306/828 | chr1 | 58682127 | ||
chr1:58682254
|
T | C | 7 | a0001a0003a0004others(4): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
missense_variant | MODERATE | c.790A>G | p.Thr264Ala | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 800/7751 | 790/2487 | 264/828 | chr1 | 58682254 | ||
chr1:58682434
|
G | A | 1 | a0008 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.610C>T | p.Arg204Cys | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 620/7751 | 610/2487 | 204/828 | chr1 | 58682434 | ||
chr1:58682446
|
A | T | 1 | a0003 | 59 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
missense_variant | MODERATE | c.598T>A | p.Cys200Ser | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 608/7751 | 598/2487 | 200/828 | chr1 | 58682446 | ||
chr1:58682464
|
T | C | 1 | a0007 | 2 | HG01256.hp1 HG04199.hp1 |
missense_variant | MODERATE | c.580A>G | p.Lys194Glu | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/20 | 590/7751 | 580/2487 | 194/828 | chr1 | 58682464 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58661414
|
G | A | 2 | a0002c0002a0008c0013 | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
synonymous_variant | LOW | c.2262C>T | p.Leu754Leu | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/20 | 2272/7751 | 2262/2487 | 754/828 | chr1 | 58661414 | ||
chr1:58676957
|
G | A | 1 | a0006c0007 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1359C>T | p.Leu453Leu | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/20 | 1369/7751 | 1359/2487 | 453/828 | chr1 | 58676957 | ||
chr1:58677041
|
T | C | 9 | a0001c0001a0003c0003a0004c0004others(6): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
synonymous_variant | LOW | c.1275A>G | p.Pro425Pro | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/20 | 1285/7751 | 1275/2487 | 425/828 | chr1 | 58677041 | ||
chr1:58700047
|
C | T | 1 | a0005c0008 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.6G>A | p.Ala2Ala | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/20 | 16/7751 | 6/2487 | 2/828 | chr1 | 58700047 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58654847
|
A | ATTAAGTA others(20): Show |
1 | a0002c0005t0015 | 5 | NA18960.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5123_*5149dupAAAA others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5149 | chr1 | 58654847 | |||||
chr1:58654891
|
A | G | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*5106T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5106 | chr1 | 58654891 | |||||
chr1:58654907
|
G | A | 88 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(85): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
3_prime_UTR_variant | MODIFIER | c.*5090C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5090 | chr1 | 58654907 | |||||
chr1:58654917
|
C | T | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*5080G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5080 | chr1 | 58654917 | |||||
chr1:58654978
|
C | T | 88 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(85): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
3_prime_UTR_variant | MODIFIER | c.*5019G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 5019 | chr1 | 58654978 | |||||
chr1:58655192
|
T | G | 2 | a0001c0001t0019a0001c0001t0056 | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4805A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4805 | chr1 | 58655192 | |||||
chr1:58655194
|
T | C | 1 | a0002c0005t0016 | 5 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4803A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4803 | chr1 | 58655194 | |||||
chr1:58655218
|
CAT | C | 3 | a0002c0005t0027a0002c0005t0029a0002c0005t0043 | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4777_*4778delAT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4777 | chr1 | 58655218 | |||||
chr1:58655289
|
G | A | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4708C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4708 | chr1 | 58655289 | |||||
chr1:58655305
|
T | C | 1 | a0002c0002t0073 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4692A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4692 | chr1 | 58655305 | |||||
chr1:58655318
|
AT | A | 85 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(82): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*4678delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4678 | chr1 | 58655318 | |||||
chr1:58655338
|
A | C | 1 | a0002c0005t0079 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4659T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4659 | chr1 | 58655338 | |||||
chr1:58655364
|
A | C | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*4633T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4633 | chr1 | 58655364 | |||||
chr1:58655365
|
C | T | 5 | a0001c0001t0036a0001c0001t0037a0001c0001t0053others(2): Show | 7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4632G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4632 | chr1 | 58655365 | |||||
chr1:58655414
|
C | T | 1 | a0002c0002t0075 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4583G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4583 | chr1 | 58655414 | |||||
chr1:58655415
|
T | C | 1 | a0002c0002t0075 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4582A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4582 | chr1 | 58655415 | |||||
chr1:58655472
|
A | AT | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4524dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4524 | chr1 | 58655472 | |||||
chr1:58655494
|
G | A | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4503C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4503 | chr1 | 58655494 | |||||
chr1:58655671
|
T | A | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*4326A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4326 | chr1 | 58655671 | |||||
chr1:58655971
|
G | A | 1 | a0001c0001t0055 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4026C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 4026 | chr1 | 58655971 | |||||
chr1:58656019
|
T | A | 1 | a0004c0004t0032 | 3 | HG02965.hp1 HG02970.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3978A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3978 | chr1 | 58656019 | |||||
chr1:58656091
|
C | T | 2 | a0004c0004t0012a0004c0004t0069 | 7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3906G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3906 | chr1 | 58656091 | |||||
chr1:58656096
|
G | C | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3901C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3901 | chr1 | 58656096 | |||||
chr1:58656212
|
C | T | 1 | a0001c0001t0054 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3785G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3785 | chr1 | 58656212 | |||||
chr1:58656283
|
T | A | 1 | a0009c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3714A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3714 | chr1 | 58656283 | |||||
chr1:58656288
|
T | G | 1 | a0001c0001t0049 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3709A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3709 | chr1 | 58656288 | |||||
chr1:58656384
|
GAAGT | G | 2 | a0002c0002t0044a0002c0002t0077 | 3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3609_*3612delACTT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3609 | chr1 | 58656384 | |||||
chr1:58656445
|
AAGGTAGT | A | 3 | a0004c0004t0024a0004c0004t0066a0004c0004t0071 | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3545_*3551delACTA others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3545 | chr1 | 58656445 | |||||
chr1:58656578
|
A | G | 1 | a0006c0007t0025 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3419T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3419 | chr1 | 58656578 | |||||
chr1:58656599
|
G | A | 1 | a0009c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3398C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3398 | chr1 | 58656599 | |||||
chr1:58656617
|
T | G | 43 | a0003c0003t0003a0003c0003t0007a0003c0003t0010others(40): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3380A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3380 | chr1 | 58656617 | |||||
chr1:58656799
|
C | A | 1 | a0009c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3198G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3198 | chr1 | 58656799 | |||||
chr1:58656891
|
A | C | 1 | a0003c0003t0067 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3106T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 3106 | chr1 | 58656891 | |||||
chr1:58657052
|
T | G | 1 | a0003c0003t0059 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2945 | chr1 | 58657052 | |||||
chr1:58657120
|
G | A | 2 | a0001c0001t0019a0001c0001t0056 | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2877C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2877 | chr1 | 58657120 | |||||
chr1:58657199
|
C | T | 68 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(65): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*2798G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2798 | chr1 | 58657199 | |||||
chr1:58657203
|
G | C | 1 | a0003c0003t0062 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2794C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2794 | chr1 | 58657203 | |||||
chr1:58657238
|
G | GA | 82 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(79): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*2758dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2758 | chr1 | 58657238 | |||||
chr1:58657311
|
C | T | 1 | a0009c0012t0048 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2686G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2686 | chr1 | 58657311 | |||||
chr1:58657338
|
T | G | 1 | a0004c0004t0068 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2659A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2659 | chr1 | 58657338 | |||||
chr1:58657574
|
G | A | 3 | a0002c0002t0028a0002c0002t0074a0002c0002t0083 | 5 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2423C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2423 | chr1 | 58657574 | |||||
chr1:58657646
|
T | C | 3 | a0002c0005t0027a0002c0005t0029a0002c0005t0043 | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2351A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2351 | chr1 | 58657646 | |||||
chr1:58657652
|
TTG | T | 3 | a0004c0004t0024a0004c0004t0066a0004c0004t0071 | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2343_*2344delCA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2343 | chr1 | 58657652 | |||||
chr1:58657697
|
TTC | T | 2 | a0001c0001t0019a0001c0001t0056 | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2298_*2299delGA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2298 | chr1 | 58657697 | |||||
chr1:58657743
|
G | A | 1 | a0003c0003t0065 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2254C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2254 | chr1 | 58657743 | |||||
chr1:58657859
|
T | C | 6 | a0004c0004t0012a0004c0004t0031a0004c0004t0032others(3): Show | 15 | HG01167.hp1 HG01255.hp2 HG01256.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2138A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2138 | chr1 | 58657859 | |||||
chr1:58657961
|
T | C | 3 | a0004c0004t0012a0004c0004t0069a0004c0004t0072 | 8 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2036A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2036 | chr1 | 58657961 | |||||
chr1:58657983
|
C | T | 15 | a0002c0002t0002a0002c0002t0005a0002c0002t0013others(12): Show | 95 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2014G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 2014 | chr1 | 58657983 | |||||
chr1:58658108
|
C | T | 1 | a0006c0007t0025 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1889G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1889 | chr1 | 58658108 | |||||
chr1:58658299
|
C | T | 2 | a0004c0004t0039a0004c0004t0063 | 3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1698G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1698 | chr1 | 58658299 | |||||
chr1:58658323
|
A | G | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1674T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1674 | chr1 | 58658323 | |||||
chr1:58658333
|
C | CT | 3 | a0002c0005t0027a0002c0005t0029a0002c0005t0043 | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1663dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1663 | chr1 | 58658333 | |||||
chr1:58658436
|
TGGAA | T | 3 | a0001c0001t0036a0001c0001t0053a0001c0001t0057 | 4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1557_*1560delTTCC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1557 | chr1 | 58658436 | |||||
chr1:58658551
|
G | A | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1446C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1446 | chr1 | 58658551 | |||||
chr1:58658589
|
T | C | 1 | a0002c0005t0015 | 5 | NA18960.hp1 NA18985.hp1 NA18998.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1408A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1408 | chr1 | 58658589 | |||||
chr1:58658701
|
GA | G | 23 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(20): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1295delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1295 | chr1 | 58658701 | |||||
chr1:58658801
|
G | A | 3 | a0002c0002t0045a0002c0002t0076a0002c0002t0078 | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1196C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1196 | chr1 | 58658801 | |||||
chr1:58658874
|
A | G | 68 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(65): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1123T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1123 | chr1 | 58658874 | |||||
chr1:58658883
|
GAAT | G | 4 | a0004c0004t0020a0004c0004t0023a0004c0004t0040others(1): Show | 10 | HG00738.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1111_*1113delATT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1111 | chr1 | 58658883 | |||||
chr1:58658924
|
T | A | 1 | a0002c0002t0041 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1073 | chr1 | 58658924 | |||||
chr1:58658958
|
A | AAC | 3 | a0002c0002t0077a0002c0002t0078a0002c0005t0030 | 5 | HG02723.hp1 HG06807.hp2 NA18949.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1038dupGT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACAC | 3 | a0001c0001t0018a0002c0002t0076a0002c0005t0029 | 8 | HG02615.hp1 HG02738.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1035_*1038dupGTGT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACAC | 14 | a0001c0001t0021a0001c0001t0037a0001c0001t0057others(11): Show | 36 | HG00735.hp1 HG01074.hp1 HG01167.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1038dupGTGT others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(1): Show |
13 | a0001c0001t0009a0001c0001t0050a0002c0002t0042others(10): Show | 33 | HG00099.hp2 HG01496.hp2 HG01884.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1038dupGTGT others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(3): Show |
19 | a0001c0001t0001a0001c0001t0036a0001c0001t0049others(16): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1029_*1038dupGTGT others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(5): Show |
16 | a0001c0001t0004a0001c0001t0019a0001c0001t0053others(13): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1027_*1038dupGTGT others(8): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(7): Show |
8 | a0001c0001t0008a0002c0002t0014a0002c0002t0074others(5): Show | 34 | HG00544.hp1 HG00639.hp2 HG00738.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1025_*1038dupGTGT others(10): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(9): Show |
3 | a0001c0001t0017a0003c0003t0022a0003c0003t0062 | 8 | HG01123.hp1 HG01361.hp2 HG02080.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1038dupGTGT others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(11): Show |
1 | a0002c0002t0073 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021_*1038dupGTGT others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | AACACACA others(13): Show |
1 | a0001c0001t0047 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019_*1038dupGTGT others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0033a0009c0012t0048 | 3 | NA18974.hp2 NA19070.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1038_*1039insGTGT others(7): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1038 | chr1 | 58658958 | |||||
chr1:58658958
|
AACAC | A | 4 | a0001c0001t0051a0002c0005t0016a0002c0005t0079others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01515.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1035_*1038delGTGT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1035 | chr1 | 58658958 | |||||
chr1:58658958
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0052 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029_*1038delGTGT others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1029 | chr1 | 58658958 | |||||
chr1:58658995
|
A | ACACACAC others(6): Show |
2 | a0001c0001t0046a0004c0004t0061 | 2 | HG03098.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1001_*1002insGTGT others(9): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 1001 | chr1 | 58658995 | |||||
chr1:58659010
|
A | G | 1 | a0004c0004t0060 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*987T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 987 | chr1 | 58659010 | |||||
chr1:58659119
|
CT | C | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*877delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 877 | chr1 | 58659119 | |||||
chr1:58659131
|
C | T | 68 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(65): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*866G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 866 | chr1 | 58659131 | |||||
chr1:58659145
|
CT | C | 3 | a0004c0004t0031a0004c0004t0032a0004c0004t0081 | 7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*851delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 851 | chr1 | 58659145 | |||||
chr1:58659278
|
C | T | 2 | a0003c0003t0058a0003c0003t0059 | 2 | HG02040.hp2 NA18947.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 719 | chr1 | 58659278 | |||||
chr1:58659578
|
C | A | 1 | a0003c0003t0082 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 419 | chr1 | 58659578 | |||||
chr1:58659638
|
A | G | 1 | a0003c0003t0038 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*359T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 359 | chr1 | 58659638 | |||||
chr1:58659647
|
C | T | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 350 | chr1 | 58659647 | |||||
chr1:58659707
|
C | T | 1 | a0003c0003t0035 | 2 | NA19084.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 290 | chr1 | 58659707 | |||||
chr1:58659843
|
C | T | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(14): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*154G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 154 | chr1 | 58659843 | |||||
chr1:58659860
|
T | C | 1 | a0002c0002t0083 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 20/20 | 137 | chr1 | 58659860 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58660162
|
G | T | 7 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2329-7C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660162 | ||||||
chr1:58660214
|
C | G | 1 | a0001c0001t0054g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2329-59G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660214 | ||||||
chr1:58660222
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-67T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660222 | ||||||
chr1:58660227
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-72C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660227 | ||||||
chr1:58660237
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2329-82T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660237 | ||||||
chr1:58660346
|
G | C | 7 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0037g0273others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2329-191C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660346 | ||||||
chr1:58660435
|
C | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-280G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660435 | ||||||
chr1:58660617
|
C | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2329-462G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660617 | ||||||
chr1:58660742
|
G | A | 2 | a0001c0001t0009g0230a0001c0001t0021g0193 | 2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2328+428C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660742 | ||||||
chr1:58660867
|
A | G | 1 | a0002c0002t0076g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2328+303T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660867 | ||||||
chr1:58660944
|
A | G | 338 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(335): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2328+226T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58660944 | ||||||
chr1:58661004
|
A | C | 338 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(335): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2328+166T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58661004 | ||||||
chr1:58661074
|
T | C | 4 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2328+96A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 19/19 | chr1 | 58661074 | ||||||
chr1:58661285
|
T | A | 2 | a0002c0005t0006g0249a0002c0005t0006g0265 | 2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2271-58A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/19 | chr1 | 58661285 | ||||||
chr1:58661301
|
C | T | 7 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.2271-74G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/19 | chr1 | 58661301 | ||||||
chr1:58661352
|
T | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2270+54A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 18/19 | chr1 | 58661352 | ||||||
chr1:58661521
|
C | T | 91 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(88): Show | 95 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2165-10G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661521 | ||||||
chr1:58661535
|
T | C | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2165-24A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661535 | ||||||
chr1:58661602
|
T | A | 1 | a0009c0012t0048g0168 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2165-91A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661602 | ||||||
chr1:58661652
|
G | A | 4 | a0004c0004t0007g0026a0004c0004t0007g0322a0004c0004t0007g0323others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-141C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661652 | ||||||
chr1:58661707
|
C | T | 2 | a0003c0003t0003g0296a0003c0003t0007g0295 | 2 | NA18945.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2165-196G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661707 | ||||||
chr1:58661748
|
A | G | 2 | a0003c0003t0003g0296a0003c0003t0007g0295 | 2 | NA18945.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2165-237T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661748 | ||||||
chr1:58661760
|
C | T | 5 | a0002c0005t0027g0021a0002c0005t0027g0251a0002c0005t0029g0022others(2): Show | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2165-249G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661760 | ||||||
chr1:58661827
|
A | T | 1 | a0004c0004t0003g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2165-316T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661827 | ||||||
chr1:58661878
|
C | G | 1 | a0005c0006t0011g0360 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2165-367G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661878 | ||||||
chr1:58661965
|
T | G | 240 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2165-454A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661965 | ||||||
chr1:58661969
|
TG | T | 91 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(88): Show | 95 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2165-459delC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661969 | ||||||
chr1:58661970
|
G | T | 2 | a0002c0002t0044g0006a0002c0002t0077g0046 | 3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2165-459C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58661970 | ||||||
chr1:58662032
|
G | A | 1 | a0002c0002t0044g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2165-521C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662032 | ||||||
chr1:58662033
|
C | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2165-522G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662033 | ||||||
chr1:58662264
|
G | A | 80 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(77): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2165-753C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662264 | ||||||
chr1:58662303
|
C | A | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-792G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662303 | ||||||
chr1:58662383
|
C | A | 1 | a0004c0004t0003g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2165-872G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662383 | ||||||
chr1:58662434
|
T | C | 1 | a0002c0002t0028g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2165-923A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662434 | ||||||
chr1:58662461
|
CCT | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(123): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2165-952_2165-951d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662461 | ||||||
chr1:58662462
|
C | CT | 183 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(180): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2165-952dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662462 | ||||||
chr1:58662462
|
C | T | 3 | a0002c0002t0002g0103a0002c0002t0014g0102a0004c0004t0007g0335 | 3 | HG00639.hp2 HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2165-951G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662462 | ||||||
chr1:58662493
|
A | G | 1 | a0002c0002t0002g0114 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2165-982T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662493 | ||||||
chr1:58662521
|
A | C | 93 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(90): Show | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2165-1010T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662521 | ||||||
chr1:58662565
|
G | A | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2165-1054C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662565 | ||||||
chr1:58662598
|
C | T | 8 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(5): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2165-1087G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662598 | ||||||
chr1:58662603
|
A | T | 4 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(1): Show | 4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2165-1092T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662603 | ||||||
chr1:58662659
|
G | GA | 7 | a0001c0001t0004g0203a0001c0001t0019g0268a0001c0001t0019g0269others(4): Show | 7 | NA18953.hp2 NA18954.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2165-1149dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662659 | ||||||
chr1:58662659
|
GA | G | 5 | a0004c0004t0020g0346a0004c0004t0020g0347a0004c0004t0020g0350others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165-1149delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662659 | ||||||
chr1:58662773
|
G | A | 3 | a0006c0007t0025g0045a0006c0007t0025g0047a0006c0007t0025g0048 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2165-1262C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662773 | ||||||
chr1:58662791
|
A | C | 1 | a0003c0003t0007g0289 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2165-1280T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662791 | ||||||
chr1:58662857
|
A | G | 8 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(5): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2165-1346T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662857 | ||||||
chr1:58662972
|
A | T | 1 | a0002c0002t0002g0079 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2165-1461T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58662972 | ||||||
chr1:58663321
|
A | G | 5 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(2): Show | 5 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-1810T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663321 | ||||||
chr1:58663328
|
T | TC | 338 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(335): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2165-1818dupG | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663328 | ||||||
chr1:58663378
|
C | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2165-1867G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663378 | ||||||
chr1:58663435
|
T | A | 1 | a0003c0003t0010g0310 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2165-1924A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663435 | ||||||
chr1:58663518
|
G | A | 4 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+1981C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663518 | ||||||
chr1:58663587
|
T | C | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2164+1912A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663587 | ||||||
chr1:58663670
|
T | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2164+1829A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663670 | ||||||
chr1:58663693
|
A | G | 3 | a0004c0004t0039g0354a0004c0004t0039g0355a0004c0004t0063g0353 | 3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2164+1806T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663693 | ||||||
chr1:58663844
|
G | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.2164+1655C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663844 | ||||||
chr1:58663947
|
T | C | 1 | a0002c0002t0076g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2164+1552A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663947 | ||||||
chr1:58663972
|
A | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.2164+1527T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663972 | ||||||
chr1:58663973
|
A | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2164+1526T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58663973 | ||||||
chr1:58664168
|
T | C | 13 | a0002c0002t0002g0066a0002c0002t0002g0078a0002c0002t0002g0079others(10): Show | 14 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.2164+1331A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664168 | ||||||
chr1:58664301
|
A | G | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+1198T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664301 | ||||||
chr1:58664368
|
G | A | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164+1131C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664368 | ||||||
chr1:58664522
|
C | T | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2164+977G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664522 | ||||||
chr1:58664550
|
A | C | 3 | a0006c0007t0025g0045a0006c0007t0025g0047a0006c0007t0025g0048 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2164+949T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664550 | ||||||
chr1:58664557
|
A | C | 116 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0078g0040others(113): Show | 133 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.2164+942T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664557 | ||||||
chr1:58664574
|
T | G | 5 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(2): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164+925A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664574 | ||||||
chr1:58664686
|
C | T | 4 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(1): Show | 4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+813G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664686 | ||||||
chr1:58664735
|
C | T | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+764G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664735 | ||||||
chr1:58664800
|
T | C | 4 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+699A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664800 | ||||||
chr1:58664942
|
C | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.2164+557G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664942 | ||||||
chr1:58664992
|
G | A | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+507C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58664992 | ||||||
chr1:58665128
|
T | C | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164+371A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665128 | ||||||
chr1:58665314
|
T | C | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+185A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665314 | ||||||
chr1:58665416
|
A | G | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+83T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665416 | ||||||
chr1:58665417
|
A | C | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2164+82T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 17/19 | chr1 | 58665417 | ||||||
chr1:58665639
|
G | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
splice_region_variant&intron_variant | LOW | c.2032-8C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665639 | ||||||
chr1:58665722
|
G | T | 1 | a0001c0001t0057g0042 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2032-91C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665722 | ||||||
chr1:58665782
|
C | T | 1 | a0002c0002t0041g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2032-151G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665782 | ||||||
chr1:58665809
|
C | T | 240 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2032-178G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665809 | ||||||
chr1:58665851
|
G | A | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2032-220C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665851 | ||||||
chr1:58665927
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0018g0208a0001c0001t0018g0217 | 3 | HG02738.hp2 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2032-296G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665927 | ||||||
chr1:58665928
|
G | C | 2 | a0004c0004t0026g0033a0004c0004t0026g0034 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2032-297C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58665928 | ||||||
chr1:58666003
|
G | A | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2032-372C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666003 | ||||||
chr1:58666005
|
C | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2032-374G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666005 | ||||||
chr1:58666012
|
C | T | 1 | a0002c0002t0041g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2032-381G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666012 | ||||||
chr1:58666033
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2032-402C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666033 | ||||||
chr1:58666046
|
G | C | 1 | a0005c0006t0026g0362 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2032-415C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666046 | ||||||
chr1:58666057
|
TA | T | 8 | a0001c0001t0001g0158a0001c0001t0001g0229a0002c0005t0027g0021others(5): Show | 11 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2032-427delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666057 | ||||||
chr1:58666122
|
C | T | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2032-491G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666122 | ||||||
chr1:58666200
|
G | C | 2 | a0004c0004t0026g0033a0004c0004t0026g0034 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2032-569C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666200 | ||||||
chr1:58666215
|
A | G | 5 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(2): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032-584T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666215 | ||||||
chr1:58666332
|
CTT | C | 4 | a0001c0001t0001g0003a0001c0001t0009g0137a0001c0001t0009g0179others(1): Show | 6 | HG02074.hp2 NA18982.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032-703_2032-702d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666332 | ||||||
chr1:58666526
|
G | GA | 240 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2031+511dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666526 | ||||||
chr1:58666576
|
C | CT | 324 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(321): Show | 361 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.2031+461dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666576 | ||||||
chr1:58666626
|
A | T | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031+412T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666626 | ||||||
chr1:58666638
|
C | T | 80 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(77): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2031+400G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666638 | ||||||
chr1:58666644
|
G | A | 3 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0014g0054 | 3 | HG00438.hp1 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2031+394C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666644 | ||||||
chr1:58666659
|
G | C | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031+379C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666659 | ||||||
chr1:58666746
|
C | T | 2 | a0004c0004t0003g0281a0005c0006t0011g0358 | 2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2031+292G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666746 | ||||||
chr1:58666883
|
A | T | 112 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(109): Show | 129 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2031+155T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666883 | ||||||
chr1:58666884
|
A | T | 1 | a0003c0003t0010g0310 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2031+154T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666884 | ||||||
chr1:58666885
|
T | A | 239 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(236): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2031+153A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666885 | ||||||
chr1:58666887
|
A | T | 112 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(109): Show | 129 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2031+151T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666887 | ||||||
chr1:58666888
|
T | A | 112 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(109): Show | 129 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2031+150A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666888 | ||||||
chr1:58666895
|
A | T | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2031+143T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666895 | ||||||
chr1:58666897
|
T | A | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2031+141A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666897 | ||||||
chr1:58666964
|
AAAGTTT | A | 11 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2031+68_2031+73del others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 16/19 | chr1 | 58666964 | ||||||
chr1:58667234
|
C | T | 15 | a0004c0004t0003g0025a0004c0004t0003g0277a0004c0004t0003g0281others(12): Show | 16 | HG01074.hp2 HG01081.hp1 HG02886.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1843-8G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667234 | ||||||
chr1:58667352
|
T | G | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1843-126A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667352 | ||||||
chr1:58667438
|
CATA | C | 6 | a0004c0004t0031g0028a0004c0004t0031g0341a0004c0004t0032g0339others(3): Show | 7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1843-215_1843-213d others(5): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667438 | ||||||
chr1:58667551
|
T | C | 1 | a0001c0001t0009g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1842+296A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667551 | ||||||
chr1:58667596
|
A | G | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1842+251T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667596 | ||||||
chr1:58667667
|
C | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1842+180G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667667 | ||||||
chr1:58667766
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1842+81A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667766 | ||||||
chr1:58667771
|
A | G | 1 | a0004c0004t0007g0338 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1842+76T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667771 | ||||||
chr1:58667822
|
CA | C | 4 | a0004c0004t0020g0346a0004c0004t0020g0347a0004c0004t0020g0350others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+24delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 15/19 | chr1 | 58667822 | ||||||
chr1:58667966
|
C | T | 8 | a0002c0002t0002g0078a0002c0002t0002g0079a0002c0002t0005g0007others(5): Show | 9 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.1768-45G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58667966 | ||||||
chr1:58668110
|
T | C | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1768-189A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668110 | ||||||
chr1:58668301
|
T | C | 1 | a0001c0001t0001g0018 | 2 | NA18968.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1767+331A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668301 | ||||||
chr1:58668408
|
T | C | 8 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(5): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1767+224A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668408 | ||||||
chr1:58668433
|
AATTT | A | 4 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1767+195_1767+198d others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668433 | ||||||
chr1:58668475
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0009g0137a0001c0001t0009g0179others(1): Show | 6 | HG02074.hp2 NA18982.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1767+157A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668475 | ||||||
chr1:58668623
|
T | G | 2 | a0003c0003t0003g0294a0003c0003t0003g0300 | 2 | NA18998.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1767+9A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 14/19 | chr1 | 58668623 | ||||||
chr1:58668698
|
C | A | 1 | a0003c0003t0010g0310 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1717-16G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668698 | ||||||
chr1:58668699
|
A | C | 1 | a0003c0003t0010g0310 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1717-17T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668699 | ||||||
chr1:58668914
|
G | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1716+70C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668914 | ||||||
chr1:58668935
|
C | CAG | 366 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(363): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.1716+48_1716+49ins others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668935 | ||||||
chr1:58668943
|
C | T | 6 | a0004c0004t0031g0028a0004c0004t0031g0341a0004c0004t0032g0339others(3): Show | 7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1716+41G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668943 | ||||||
chr1:58668978
|
T | C | 2 | a0004c0004t0012g0366a0004c0004t0012g0368 | 2 | HG01167.hp1 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1716+6A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 13/19 | chr1 | 58668978 | ||||||
chr1:58669219
|
CA | C | 113 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(110): Show | 130 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1662-182delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669219 | ||||||
chr1:58669312
|
T | C | 3 | a0006c0007t0025g0045a0006c0007t0025g0047a0006c0007t0025g0048 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1662-274A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669312 | ||||||
chr1:58669439
|
C | T | 15 | a0004c0004t0003g0025a0004c0004t0003g0277a0004c0004t0003g0281others(12): Show | 16 | HG01074.hp2 HG01081.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.1662-401G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669439 | ||||||
chr1:58669532
|
C | A | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1662-494G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669532 | ||||||
chr1:58669657
|
C | T | 1 | a0004c0004t0003g0317 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1662-619G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669657 | ||||||
chr1:58669825
|
G | T | 80 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(77): Show | 95 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1662-787C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669825 | ||||||
chr1:58669836
|
C | CA | 11 | a0002c0005t0006g0242a0002c0005t0006g0252a0002c0005t0006g0256others(8): Show | 14 | HG00140.hp2 HG01074.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662-799dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669836 | ||||||
chr1:58669853
|
A | C | 4 | a0002c0005t0016g0254a0002c0005t0016g0255a0002c0005t0016g0257others(1): Show | 4 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662-815T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669853 | ||||||
chr1:58669857
|
A | AAAAC | 36 | a0001c0001t0001g0015a0001c0001t0001g0183a0001c0001t0001g0197others(33): Show | 39 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | ||||||
chr1:58669857
|
A | AAAC | 107 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(104): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(5): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | ||||||
chr1:58669857
|
A | AAC | 77 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0134others(74): Show | 93 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | ||||||
chr1:58669857
|
A | AC | 71 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0052others(68): Show | 74 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1662-820_1662-819i others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | ||||||
chr1:58669857
|
A | C | 36 | a0001c0001t0009g0170a0001c0001t0019g0268a0001c0001t0019g0269others(33): Show | 39 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1662-819T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669857 | ||||||
chr1:58669863
|
C | A | 1 | a0003c0003t0010g0310 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1662-825G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669863 | ||||||
chr1:58669864
|
A | C | 1 | a0003c0003t0010g0310 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1662-826T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669864 | ||||||
chr1:58669970
|
T | C | 93 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(90): Show | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1662-932A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58669970 | ||||||
chr1:58670151
|
G | A | 2 | a0003c0003t0058g0301a0003c0003t0059g0302 | 2 | HG02040.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662-1113C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670151 | ||||||
chr1:58670162
|
A | G | 1 | a0002c0002t0044g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1662-1124T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670162 | ||||||
chr1:58670252
|
A | G | 3 | a0004c0004t0032g0339a0004c0004t0032g0342a0004c0004t0032g0343 | 3 | HG02965.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1662-1214T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670252 | ||||||
chr1:58670343
|
A | C | 8 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(5): Show | 8 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662-1305T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670343 | ||||||
chr1:58670639
|
C | T | 93 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(90): Show | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1661+1231G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670639 | ||||||
chr1:58670677
|
C | G | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+1193G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670677 | ||||||
chr1:58670757
|
A | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1661+1113T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670757 | ||||||
chr1:58670759
|
T | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1661+1111A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670759 | ||||||
chr1:58670774
|
A | T | 11 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1661+1096T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670774 | ||||||
chr1:58670978
|
T | C | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661+892A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58670978 | ||||||
chr1:58671166
|
C | A | 2 | a0003c0003t0003g0303a0003c0003t0007g0285 | 2 | HG02004.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1661+704G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671166 | ||||||
chr1:58671203
|
C | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1661+667G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671203 | ||||||
chr1:58671232
|
G | A | 87 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(84): Show | 91 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1661+638C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671232 | ||||||
chr1:58671240
|
G | C | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+630C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671240 | ||||||
chr1:58671277
|
A | G | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+593T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671277 | ||||||
chr1:58671439
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1661+431A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671439 | ||||||
chr1:58671448
|
G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1661+422C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671448 | ||||||
chr1:58671538
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1661+332G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671538 | ||||||
chr1:58671601
|
C | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1661+269G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671601 | ||||||
chr1:58671628
|
C | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0004g0138others(1): Show | 4 | HG02027.hp1 HG02135.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1661+242G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671628 | ||||||
chr1:58671665
|
T | C | 1 | a0001c0001t0004g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1661+205A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671665 | ||||||
chr1:58671723
|
C | T | 5 | a0002c0005t0027g0021a0002c0005t0027g0251a0002c0005t0029g0022others(2): Show | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661+147G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671723 | ||||||
chr1:58671731
|
C | CA | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+138dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671731 | ||||||
chr1:58671754
|
G | T | 1 | a0002c0002t0044g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1661+116C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671754 | ||||||
chr1:58671757
|
G | C | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+113C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671757 | ||||||
chr1:58671784
|
T | C | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1661+86A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671784 | ||||||
chr1:58671792
|
A | T | 1 | a0004c0004t0023g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1661+78T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 12/19 | chr1 | 58671792 | ||||||
chr1:58672072
|
T | A | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1573-114A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672072 | ||||||
chr1:58672111
|
A | G | 240 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1573-153T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672111 | ||||||
chr1:58672126
|
T | A | 8 | a0002c0002t0002g0078a0002c0002t0002g0079a0002c0002t0005g0007others(5): Show | 9 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.1573-168A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672126 | ||||||
chr1:58672132
|
A | C | 7 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0037g0273others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573-174T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672132 | ||||||
chr1:58672167
|
A | C | 1 | a0002c0002t0002g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1573-209T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672167 | ||||||
chr1:58672315
|
G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1573-357C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672315 | ||||||
chr1:58672500
|
C | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(330): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1573-542G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672500 | ||||||
chr1:58672553
|
A | G | 2 | a0001c0001t0037g0273a0001c0001t0037g0275 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1573-595T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672553 | ||||||
chr1:58672964
|
A | G | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572+609T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58672964 | ||||||
chr1:58673027
|
G | A | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572+546C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673027 | ||||||
chr1:58673143
|
C | A | 87 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(84): Show | 91 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1572+430G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673143 | ||||||
chr1:58673175
|
G | A | 1 | a0002c0002t0002g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1572+398C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673175 | ||||||
chr1:58673212
|
CAT | C | 69 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(66): Show | 84 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1572+359_1572+360d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673212 | ||||||
chr1:58673346
|
A | G | 1 | a0004c0004t0003g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1572+227T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673346 | ||||||
chr1:58673379
|
T | C | 1 | a0001c0001t0004g0203 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1572+194A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673379 | ||||||
chr1:58673551
|
C | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1572+22G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 11/19 | chr1 | 58673551 | ||||||
chr1:58673865
|
G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1495-215C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58673865 | ||||||
chr1:58674053
|
G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1495-403C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674053 | ||||||
chr1:58674069
|
G | A | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1495-419C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674069 | ||||||
chr1:58674092
|
T | C | 33 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(30): Show | 35 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1495-442A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674092 | ||||||
chr1:58674155
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1495-505C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674155 | ||||||
chr1:58674311
|
G | A | 1 | a0003c0003t0003g0306 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1495-661C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674311 | ||||||
chr1:58674509
|
G | C | 5 | a0004c0004t0031g0028a0004c0004t0031g0341a0004c0004t0032g0339others(2): Show | 6 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-859C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674509 | ||||||
chr1:58674513
|
A | G | 1 | a0002c0002t0028g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1495-863T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674513 | ||||||
chr1:58674619
|
T | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(57): Show | 72 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1494+858A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674619 | ||||||
chr1:58674663
|
C | T | 8 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(5): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+814G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674663 | ||||||
chr1:58674697
|
G | A | 1 | a0002c0002t0005g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1494+780C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674697 | ||||||
chr1:58674700
|
C | T | 4 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(1): Show | 4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+777G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674700 | ||||||
chr1:58674701
|
G | A | 3 | a0006c0007t0025g0045a0006c0007t0025g0047a0006c0007t0025g0048 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1494+776C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674701 | ||||||
chr1:58674722
|
G | A | 34 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0078g0040others(31): Show | 34 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1494+755C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674722 | ||||||
chr1:58674741
|
A | T | 1 | a0002c0002t0005g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1494+736T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674741 | ||||||
chr1:58674880
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(203): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1494+597A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674880 | ||||||
chr1:58674881
|
G | A | 206 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(203): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1494+596C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674881 | ||||||
chr1:58674926
|
C | CA | 6 | a0001c0001t0001g0151a0001c0001t0004g0199a0001c0001t0009g0184others(3): Show | 6 | HG02145.hp1 HG02523.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1494+550dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674926 | ||||||
chr1:58674934
|
A | AG | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1494+542_1494+543i others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674934 | ||||||
chr1:58674990
|
C | T | 4 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+487G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58674990 | ||||||
chr1:58675016
|
G | T | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+461C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675016 | ||||||
chr1:58675018
|
C | G | 1 | a0003c0003t0003g0294 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1494+459G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675018 | ||||||
chr1:58675051
|
A | T | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1494+426T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675051 | ||||||
chr1:58675053
|
A | G | 1 | a0003c0003t0003g0294 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1494+424T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675053 | ||||||
chr1:58675334
|
C | T | 2 | a0005c0006t0011g0358a0005c0008t0010g0005 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1494+143G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675334 | ||||||
chr1:58675353
|
A | T | 20 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(17): Show | 21 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1494+124T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675353 | ||||||
chr1:58675412
|
C | T | 4 | a0002c0002t0002g0125a0002c0002t0013g0126a0004c0004t0026g0033others(1): Show | 4 | HG02630.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+65G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 10/19 | chr1 | 58675412 | ||||||
chr1:58675693
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(122): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1391-113C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58675693 | ||||||
chr1:58675944
|
G | A | 1 | a0002c0002t0044g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1391-364C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58675944 | ||||||
chr1:58676146
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1391-566G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676146 | ||||||
chr1:58676147
|
G | A | 2 | a0002c0002t0002g0009a0002c0002t0005g0105 | 3 | HG01516.hp2 HG01517.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1391-567C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676147 | ||||||
chr1:58676154
|
C | G | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1391-574G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676154 | ||||||
chr1:58676241
|
A | AC | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1391-662dupG | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676241 | ||||||
chr1:58676308
|
C | T | 2 | a0003c0003t0003g0306a0003c0003t0003g0330 | 2 | NA18948.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1390+618G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676308 | ||||||
chr1:58676359
|
T | G | 1 | a0004c0004t0072g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1390+567A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676359 | ||||||
chr1:58676372
|
C | T | 1 | a0004c0004t0003g0314 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1390+554G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676372 | ||||||
chr1:58676402
|
C | T | 1 | a0002c0005t0015g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1390+524G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676402 | ||||||
chr1:58676405
|
G | GA | 7 | a0001c0001t0001g0150a0001c0001t0004g0204a0001c0001t0009g0184others(4): Show | 10 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390+520dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676405 | ||||||
chr1:58676405
|
GA | G | 105 | a0001c0001t0001g0158a0001c0001t0001g0224a0001c0001t0036g0036others(102): Show | 110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1390+520delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676405 | ||||||
chr1:58676527
|
G | T | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1390+399C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676527 | ||||||
chr1:58676576
|
T | C | 239 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(236): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1390+350A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676576 | ||||||
chr1:58676585
|
TAGCATGA others(4): Show |
T | 1 | a0003c0003t0003g0276 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1390+330_1390+340d others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676585 | ||||||
chr1:58676710
|
C | T | 5 | a0002c0005t0027g0021a0002c0005t0027g0251a0002c0005t0029g0022others(2): Show | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390+216G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676710 | ||||||
chr1:58676892
|
C | T | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390+34G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 9/19 | chr1 | 58676892 | ||||||
chr1:58677131
|
A | G | 1 | a0001c0001t0019g0268 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1260-75T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677131 | ||||||
chr1:58677157
|
C | T | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-101G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677157 | ||||||
chr1:58677182
|
T | C | 1 | a0003c0003t0003g0305 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1260-126A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677182 | ||||||
chr1:58677334
|
T | G | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-278A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677334 | ||||||
chr1:58677336
|
C | T | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-280G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677336 | ||||||
chr1:58677360
|
T | C | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-304A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677360 | ||||||
chr1:58677428
|
T | G | 1 | a0002c0002t0076g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1260-372A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677428 | ||||||
chr1:58677455
|
C | T | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-399G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677455 | ||||||
chr1:58677513
|
T | C | 1 | a0002c0002t0014g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1260-457A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677513 | ||||||
chr1:58677519
|
ATT | A | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260-465_1260-464d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677519 | ||||||
chr1:58677663
|
C | T | 1 | a0001c0001t0055g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1260-607G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677663 | ||||||
chr1:58677704
|
C | A | 1 | a0002c0005t0027g0021 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1260-648G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677704 | ||||||
chr1:58677716
|
C | T | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-660G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677716 | ||||||
chr1:58677729
|
A | G | 77 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(74): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1260-673T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677729 | ||||||
chr1:58677942
|
C | G | 93 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(90): Show | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1260-886G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58677942 | ||||||
chr1:58678078
|
T | C | 1 | a0002c0002t0002g0114 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1260-1022A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678078 | ||||||
chr1:58678162
|
A | G | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1106T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678162 | ||||||
chr1:58678199
|
T | C | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1143A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678199 | ||||||
chr1:58678252
|
C | A | 332 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(329): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1260-1196G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678252 | ||||||
chr1:58678394
|
A | G | 1 | a0002c0002t0002g0107 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1260-1338T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678394 | ||||||
chr1:58678481
|
G | A | 1 | a0003c0003t0003g0306 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1260-1425C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678481 | ||||||
chr1:58678674
|
A | G | 1 | a0003c0003t0003g0318 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1260-1618T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678674 | ||||||
chr1:58678764
|
G | A | 66 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(63): Show | 81 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1260-1708C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678764 | ||||||
chr1:58678793
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1260-1737G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678793 | ||||||
chr1:58678806
|
A | C | 1 | a0001c0001t0054g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1260-1750T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678806 | ||||||
chr1:58678807
|
T | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(235): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1260-1751A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678807 | ||||||
chr1:58678808
|
G | C | 1 | a0003c0003t0003g0307 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1260-1752C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678808 | ||||||
chr1:58678821
|
C | T | 1 | a0001c0001t0004g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1260-1765G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678821 | ||||||
chr1:58678832
|
T | G | 1 | a0001c0001t0008g0157 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1260-1776A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678832 | ||||||
chr1:58678916
|
G | A | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1860C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58678916 | ||||||
chr1:58679007
|
A | C | 5 | a0004c0004t0020g0346a0004c0004t0020g0347a0004c0004t0020g0350others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260-1951T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679007 | ||||||
chr1:58679009
|
G | A | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1953C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679009 | ||||||
chr1:58679016
|
A | G | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-1960T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679016 | ||||||
chr1:58679018
|
A | G | 1 | a0003c0003t0062g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1260-1962T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679018 | ||||||
chr1:58679026
|
C | T | 1 | a0002c0005t0029g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1260-1970G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679026 | ||||||
chr1:58679115
|
A | G | 239 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(236): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1260-2059T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679115 | ||||||
chr1:58679249
|
C | A | 32 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(29): Show | 34 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260-2193G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679249 | ||||||
chr1:58679387
|
C | T | 3 | a0002c0005t0006g0242a0002c0005t0006g0246a0002c0005t0006g0262 | 3 | NA18965.hp1 NA18974.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1260-2331G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679387 | ||||||
chr1:58679534
|
C | T | 4 | a0004c0004t0003g0312a0004c0004t0003g0331a0004c0004t0010g0313others(1): Show | 4 | HG02895.hp2 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259+2251G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679534 | ||||||
chr1:58679679
|
G | C | 7 | a0002c0002t0002g0115a0002c0002t0002g0125a0002c0002t0005g0124others(4): Show | 8 | HG00642.hp1 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1259+2106C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679679 | ||||||
chr1:58679682
|
C | A | 1 | a0004c0004t0066g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1259+2103G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679682 | ||||||
chr1:58679749
|
C | T | 1 | a0003c0003t0065g0293 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1259+2036G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679749 | ||||||
chr1:58679780
|
A | C | 239 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(236): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1259+2005T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679780 | ||||||
chr1:58679898
|
C | G | 1 | a0001c0001t0004g0218 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1259+1887G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679898 | ||||||
chr1:58679971
|
G | C | 2 | a0003c0003t0035g0332a0003c0003t0035g0334 | 2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1259+1814C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58679971 | ||||||
chr1:58680006
|
G | T | 1 | a0001c0001t0001g0003 | 3 | NA18982.hp1 NA18999.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1259+1779C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680006 | ||||||
chr1:58680026
|
C | CAAA | 11 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(8): Show | 12 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1259+1756_1259+175 others(7): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | ||||||
chr1:58680026
|
CA | C | 97 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(94): Show | 104 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1259+1758delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | ||||||
chr1:58680026
|
CAAAAAAA others(4): Show |
C | 206 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(203): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1259+1748_1259+175 others(15): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | ||||||
chr1:58680026
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1259+1747_1259+175 others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680026 | ||||||
chr1:58680176
|
T | C | 4 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259+1609A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680176 | ||||||
chr1:58680212
|
T | C | 1 | a0003c0003t0007g0308 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1259+1573A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680212 | ||||||
chr1:58680277
|
T | A | 77 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(74): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1259+1508A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680277 | ||||||
chr1:58680286
|
C | A | 332 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(329): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1259+1499G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680286 | ||||||
chr1:58680514
|
T | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(210): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1259+1271A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680514 | ||||||
chr1:58680523
|
T | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1259+1262A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680523 | ||||||
chr1:58680549
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(322): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1259+1236T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680549 | ||||||
chr1:58680637
|
T | C | 75 | a0001c0001t0001g0196a0002c0002t0002g0078a0002c0002t0002g0079others(72): Show | 91 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1259+1148A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680637 | ||||||
chr1:58680644
|
C | T | 1 | a0001c0001t0054g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+1141G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680644 | ||||||
chr1:58680744
|
T | C | 121 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0141others(118): Show | 129 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1259+1041A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680744 | ||||||
chr1:58680752
|
T | C | 1 | a0001c0001t0054g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1259+1033A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680752 | ||||||
chr1:58680824
|
A | AT | 154 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(151): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1259+960dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680824 | ||||||
chr1:58680824
|
AT | A | 19 | a0002c0002t0002g0052a0002c0002t0002g0063a0002c0002t0002g0065others(16): Show | 19 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1259+960delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680824 | ||||||
chr1:58680928
|
T | C | 1 | a0002c0005t0006g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1259+857A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58680928 | ||||||
chr1:58681019
|
A | G | 1 | a0003c0003t0062g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1259+766T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681019 | ||||||
chr1:58681172
|
A | T | 2 | a0004c0004t0026g0033a0004c0004t0026g0034 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1259+613T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681172 | ||||||
chr1:58681335
|
T | C | 1 | a0001c0001t0004g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1259+450A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681335 | ||||||
chr1:58681339
|
A | G | 6 | a0004c0004t0031g0028a0004c0004t0031g0341a0004c0004t0032g0339others(3): Show | 7 | HG01256.hp2 HG01258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1259+446T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681339 | ||||||
chr1:58681409
|
C | A | 77 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(74): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1259+376G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681409 | ||||||
chr1:58681462
|
G | A | 2 | a0001c0001t0009g0230a0001c0001t0021g0193 | 2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1259+323C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681462 | ||||||
chr1:58681748
|
G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1259+37C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 8/19 | chr1 | 58681748 | ||||||
chr1:58682601
|
C | G | 1 | a0001c0001t0009g0230 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.499-56G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682601 | ||||||
chr1:58682650
|
A | G | 4 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(1): Show | 5 | HG02257.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-105T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682650 | ||||||
chr1:58682679
|
G | A | 10 | a0002c0005t0006g0242a0002c0005t0006g0245a0002c0005t0006g0246others(7): Show | 10 | HG00673.hp1 NA18946.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.499-134C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682679 | ||||||
chr1:58682679
|
GCTTTTCT others(7): Show |
G | 114 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(111): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.499-148_499-135del others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682679 | ||||||
chr1:58682685
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0194a0001c0001t0004g0166 | 2 | HG01169.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.499-155_499-141del others(15): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682685 | ||||||
chr1:58682686
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0009g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.499-154_499-142del others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682686 | ||||||
chr1:58682788
|
C | T | 4 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(1): Show | 5 | HG02257.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-243G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682788 | ||||||
chr1:58682789
|
G | A | 4 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(1): Show | 4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-244C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682789 | ||||||
chr1:58682807
|
T | G | 1 | a0006c0010t0010g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.499-262A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682807 | ||||||
chr1:58682936
|
G | C | 339 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(336): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.499-391C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682936 | ||||||
chr1:58682946
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.499-401G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58682946 | ||||||
chr1:58683007
|
T | C | 2 | a0003c0003t0003g0276a0003c0003t0010g0310 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.499-462A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683007 | ||||||
chr1:58683038
|
G | T | 1 | a0007c0009t0001g0227 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.499-493C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683038 | ||||||
chr1:58683187
|
T | C | 1 | a0001c0001t0009g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.499-642A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683187 | ||||||
chr1:58683338
|
T | C | 1 | a0002c0002t0077g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499-793A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683338 | ||||||
chr1:58683394
|
G | A | 1 | a0004c0004t0007g0335 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.499-849C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683394 | ||||||
chr1:58683582
|
A | AATGAGCA others(3): Show |
1 | a0002c0002t0005g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499-1047_499-1038d others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683582 | ||||||
chr1:58683585
|
G | T | 1 | a0002c0005t0027g0021 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.499-1040C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683585 | ||||||
chr1:58683865
|
G | C | 2 | a0002c0005t0006g0253a0002c0005t0006g0263 | 2 | NA18946.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.498+1288C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683865 | ||||||
chr1:58683887
|
A | T | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+1266T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683887 | ||||||
chr1:58683889
|
A | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(199): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.498+1264T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683889 | ||||||
chr1:58683939
|
T | A | 3 | a0001c0001t0009g0184a0007c0009t0001g0195a0007c0009t0001g0227 | 3 | HG01256.hp1 HG02145.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.498+1214A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683939 | ||||||
chr1:58683940
|
C | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(199): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.498+1213G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683940 | ||||||
chr1:58683992
|
A | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.498+1161T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58683992 | ||||||
chr1:58684061
|
G | T | 77 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(74): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.498+1092C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684061 | ||||||
chr1:58684152
|
G | A | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+1001C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684152 | ||||||
chr1:58684166
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(334): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.498+987G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684166 | ||||||
chr1:58684293
|
C | T | 94 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(91): Show | 98 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.498+860G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684293 | ||||||
chr1:58684326
|
G | A | 1 | a0002c0002t0002g0052 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.498+827C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684326 | ||||||
chr1:58684355
|
G | A | 5 | a0004c0004t0020g0346a0004c0004t0020g0347a0004c0004t0020g0350others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+798C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684355 | ||||||
chr1:58684382
|
G | A | 2 | a0001c0001t0009g0198a0001c0001t0009g0216 | 2 | NA18952.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.498+771C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684382 | ||||||
chr1:58684433
|
C | T | 2 | a0002c0002t0002g0096a0004c0004t0007g0335 | 2 | HG00639.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.498+720G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684433 | ||||||
chr1:58684514
|
G | A | 77 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(74): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.498+639C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684514 | ||||||
chr1:58684520
|
G | A | 77 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(74): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.498+633C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684520 | ||||||
chr1:58684543
|
C | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(199): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.498+610G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684543 | ||||||
chr1:58684564
|
C | CA | 11 | a0001c0001t0008g0142a0001c0001t0036g0036a0001c0001t0053g0043others(8): Show | 13 | HG01192.hp1 HG01978.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.498+588dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684564 | ||||||
chr1:58684564
|
CA | C | 9 | a0003c0003t0003g0290a0004c0004t0012g0365a0004c0004t0012g0366others(6): Show | 9 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.498+588delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684564 | ||||||
chr1:58684608
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(122): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.498+545G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684608 | ||||||
chr1:58684811
|
A | G | 1 | a0002c0005t0079g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.498+342T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58684811 | ||||||
chr1:58685050
|
A | C | 1 | a0003c0003t0007g0289 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.498+103T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 7/19 | chr1 | 58685050 | ||||||
chr1:58685269
|
G | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(334): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.400-18C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685269 | ||||||
chr1:58685304
|
T | C | 3 | a0006c0007t0025g0045a0006c0007t0025g0047a0006c0007t0025g0048 | 3 | HG01884.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.400-53A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685304 | ||||||
chr1:58685325
|
T | TA | 34 | a0002c0005t0015g0239a0002c0005t0015g0241a0002c0005t0015g0243others(31): Show | 36 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.400-75dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685325 | ||||||
chr1:58685325
|
TA | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(203): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.400-75delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685325 | ||||||
chr1:58685437
|
T | C | 1 | a0002c0005t0006g0245 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.400-186A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685437 | ||||||
chr1:58685511
|
T | C | 1 | a0002c0002t0002g0087 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.400-260A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685511 | ||||||
chr1:58685544
|
T | C | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-293A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685544 | ||||||
chr1:58685601
|
G | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(199): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.400-350C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685601 | ||||||
chr1:58685699
|
A | G | 5 | a0002c0005t0027g0021a0002c0005t0027g0251a0002c0005t0029g0022others(2): Show | 8 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-448T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58685699 | ||||||
chr1:58686067
|
A | C | 1 | a0006c0010t0010g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.400-816T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686067 | ||||||
chr1:58686165
|
A | T | 1 | a0001c0001t0004g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.400-914T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686165 | ||||||
chr1:58686216
|
A | G | 5 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(2): Show | 5 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-965T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686216 | ||||||
chr1:58686286
|
A | C | 46 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(43): Show | 59 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400-1035T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686286 | ||||||
chr1:58686343
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.400-1092G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686343 | ||||||
chr1:58686383
|
G | A | 4 | a0004c0004t0007g0026a0004c0004t0007g0322a0004c0004t0007g0323others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-1132C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686383 | ||||||
chr1:58686462
|
T | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.400-1211A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686462 | ||||||
chr1:58686596
|
A | C | 2 | a0002c0002t0044g0006a0002c0002t0077g0046 | 3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.400-1345T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686596 | ||||||
chr1:58686795
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.400-1544C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686795 | ||||||
chr1:58686899
|
T | C | 1 | a0002c0002t0002g0112 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.400-1648A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686899 | ||||||
chr1:58686965
|
T | TA | 172 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(169): Show | 191 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.400-1715dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686965 | ||||||
chr1:58686981
|
A | C | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-1730T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58686981 | ||||||
chr1:58687037
|
A | C | 1 | a0003c0003t0011g0329 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-1786T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687037 | ||||||
chr1:58687238
|
T | C | 2 | a0002c0002t0005g0072a0002c0002t0014g0059 | 2 | NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.399+1800A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687238 | ||||||
chr1:58687275
|
A | G | 10 | a0004c0004t0020g0327a0004c0004t0020g0346a0004c0004t0020g0347others(7): Show | 10 | HG00738.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1763T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687275 | ||||||
chr1:58687338
|
G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.399+1700C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687338 | ||||||
chr1:58687342
|
G | A | 1 | a0007c0009t0001g0227 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.399+1696C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687342 | ||||||
chr1:58687351
|
T | A | 3 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0078g0040 | 3 | HG02723.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.399+1687A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687351 | ||||||
chr1:58687395
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.399+1643A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687395 | ||||||
chr1:58687505
|
A | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.399+1533T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687505 | ||||||
chr1:58687507
|
C | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(334): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.399+1531G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687507 | ||||||
chr1:58687633
|
G | T | 29 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(26): Show | 31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+1405C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687633 | ||||||
chr1:58687659
|
T | C | 15 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(12): Show | 16 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+1379A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687659 | ||||||
chr1:58687835
|
CTA | C | 29 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(26): Show | 31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+1201_399+1202d others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58687835 | ||||||
chr1:58688287
|
C | T | 2 | a0001c0001t0004g0218a0001c0001t0008g0200 | 2 | HG01099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.399+751G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688287 | ||||||
chr1:58688289
|
T | C | 2 | a0004c0004t0007g0323a0004c0004t0007g0324 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.399+749A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688289 | ||||||
chr1:58688289
|
TA | T | 3 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0078g0040 | 3 | HG02723.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.399+748delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688289 | ||||||
chr1:58688421
|
TA | T | 29 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(26): Show | 31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+616delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688421 | ||||||
chr1:58688497
|
C | T | 1 | a0004c0004t0031g0341 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.399+541G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688497 | ||||||
chr1:58688561
|
C | CA | 8 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(5): Show | 8 | HG00738.hp1 HG01192.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+476dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688561 | ||||||
chr1:58688595
|
C | T | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+443G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688595 | ||||||
chr1:58688647
|
C | A | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+391G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688647 | ||||||
chr1:58688695
|
CA | C | 250 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(247): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.399+342delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688695 | ||||||
chr1:58688695
|
CAA | C | 8 | a0001c0001t0001g0228a0002c0005t0027g0021a0002c0005t0027g0251others(5): Show | 11 | HG01074.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+341_399+342del others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688695 | ||||||
chr1:58688803
|
G | A | 1 | a0001c0001t0055g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.399+235C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688803 | ||||||
chr1:58688841
|
T | C | 1 | a0006c0007t0025g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.399+197A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 6/19 | chr1 | 58688841 | ||||||
chr1:58689275
|
C | T | 1 | a0004c0004t0020g0327 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.321-159G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689275 | ||||||
chr1:58689665
|
C | A | 2 | a0003c0003t0003g0318a0003c0003t0003g0319 | 2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.321-549G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689665 | ||||||
chr1:58689765
|
A | C | 2 | a0001c0001t0018g0208a0001c0001t0018g0217 | 2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.320+461T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689765 | ||||||
chr1:58689819
|
TA | T | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+406delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689819 | ||||||
chr1:58689843
|
C | G | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+383G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58689843 | ||||||
chr1:58690011
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.320+215A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58690011 | ||||||
chr1:58690067
|
T | C | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+159A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58690067 | ||||||
chr1:58690196
|
G | T | 1 | a0001c0001t0036g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.320+30C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 5/19 | chr1 | 58690196 | ||||||
chr1:58690282
|
G | A | 1 | a0001c0001t0049g0211 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.297-33C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 4/19 | chr1 | 58690282 | ||||||
chr1:58690465
|
A | T | 1 | a0002c0002t0002g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.219-48T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690465 | ||||||
chr1:58690483
|
C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.219-66G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690483 | ||||||
chr1:58690568
|
ATCAAGCT others(10): Show |
A | 15 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(12): Show | 16 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-168_219-152del others(17): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690568 | ||||||
chr1:58690607
|
G | A | 1 | a0009c0012t0048g0168 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.219-190C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690607 | ||||||
chr1:58690680
|
A | AT | 6 | a0001c0001t0056g0267a0002c0002t0002g0096a0002c0002t0005g0067others(3): Show | 7 | HG01891.hp2 HG06807.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-264dupA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690680 | ||||||
chr1:58690680
|
AT | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(208): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.219-264delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690680 | ||||||
chr1:58690938
|
C | A | 1 | a0003c0003t0003g0320 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.219-521G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690938 | ||||||
chr1:58690996
|
G | A | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-579C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58690996 | ||||||
chr1:58691005
|
C | T | 2 | a0002c0002t0002g0101a0002c0002t0005g0116 | 2 | NA18972.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.219-588G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691005 | ||||||
chr1:58691141
|
G | A | 15 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(12): Show | 16 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-724C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691141 | ||||||
chr1:58691153
|
G | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(199): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.219-736C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691153 | ||||||
chr1:58691204
|
TG | T | 96 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(93): Show | 101 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.219-788delC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691204 | ||||||
chr1:58691536
|
C | G | 2 | a0001c0001t0018g0169a0001c0001t0018g0186 | 2 | NA18983.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.219-1119G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691536 | ||||||
chr1:58691539
|
T | C | 1 | a0006c0010t0010g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219-1122A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691539 | ||||||
chr1:58691634
|
G | A | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1217C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691634 | ||||||
chr1:58691835
|
C | G | 29 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(26): Show | 31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+1026G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691835 | ||||||
chr1:58691978
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.218+883T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58691978 | ||||||
chr1:58692023
|
G | A | 29 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(26): Show | 31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+838C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692023 | ||||||
chr1:58692081
|
A | G | 29 | a0004c0004t0003g0349a0004c0004t0012g0365a0004c0004t0012g0366others(26): Show | 31 | HG01109.hp2 HG01167.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+780T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692081 | ||||||
chr1:58692356
|
C | T | 1 | a0002c0002t0005g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.218+505G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692356 | ||||||
chr1:58692419
|
T | C | 1 | a0002c0002t0014g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.218+442A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692419 | ||||||
chr1:58692431
|
T | C | 1 | a0002c0005t0006g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218+430A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692431 | ||||||
chr1:58692450
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0004g0147others(1): Show | 4 | HG00423.hp2 HG00609.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+411G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692450 | ||||||
chr1:58692489
|
A | G | 236 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(233): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.218+372T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692489 | ||||||
chr1:58692502
|
G | A | 7 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0037g0273others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+359C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692502 | ||||||
chr1:58692695
|
G | A | 8 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(5): Show | 8 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+166C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 3/19 | chr1 | 58692695 | ||||||
chr1:58692960
|
T | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.148-29A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58692960 | ||||||
chr1:58693390
|
G | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.148-459C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693390 | ||||||
chr1:58693413
|
C | T | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-482G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693413 | ||||||
chr1:58693470
|
A | G | 1 | a0003c0003t0007g0285 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.148-539T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693470 | ||||||
chr1:58693521
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.148-590G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693521 | ||||||
chr1:58693630
|
T | C | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-699A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693630 | ||||||
chr1:58693883
|
T | G | 1 | a0002c0005t0006g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.148-952A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58693883 | ||||||
chr1:58694020
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.148-1089G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694020 | ||||||
chr1:58694135
|
G | A | 7 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(4): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+994C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694135 | ||||||
chr1:58694150
|
ACT | A | 5 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+977_147+978del others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694150 | ||||||
chr1:58694164
|
T | A | 1 | a0001c0001t0036g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.147+965A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694164 | ||||||
chr1:58694210
|
T | C | 1 | a0003c0003t0022g0321 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.147+919A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694210 | ||||||
chr1:58694282
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(115): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.147+847A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694282 | ||||||
chr1:58694514
|
G | A | 1 | a0004c0004t0072g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147+615C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694514 | ||||||
chr1:58694611
|
G | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(233): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.147+518C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694611 | ||||||
chr1:58694617
|
C | CA | 9 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(6): Show | 9 | HG03209.hp1 HG03225.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+511dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694617 | ||||||
chr1:58694617
|
CA | C | 10 | a0001c0001t0001g0162a0001c0001t0001g0219a0001c0001t0004g0146others(7): Show | 11 | HG01516.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+511delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694617 | ||||||
chr1:58694692
|
C | T | 2 | a0001c0001t0037g0273a0001c0001t0037g0275 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.147+437G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694692 | ||||||
chr1:58694708
|
G | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(204): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.147+421C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694708 | ||||||
chr1:58694803
|
G | A | 1 | a0002c0002t0002g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.147+326C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694803 | ||||||
chr1:58694839
|
T | G | 90 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(87): Show | 94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.147+290A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694839 | ||||||
chr1:58694868
|
C | T | 1 | a0004c0004t0040g0352 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.147+261G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58694868 | ||||||
chr1:58695045
|
C | T | 1 | a0001c0001t0004g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.147+84G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695045 | ||||||
chr1:58695052
|
TA | T | 208 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(205): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.147+76delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695052 | ||||||
chr1:58695063
|
A | AG | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+65_147+66insC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695063 | ||||||
chr1:58695063
|
A | G | 129 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(126): Show | 137 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.147+66T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695063 | ||||||
chr1:58695070
|
A | C | 41 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(38): Show | 44 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.147+59T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 2/19 | chr1 | 58695070 | ||||||
chr1:58695213
|
A | G | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
splice_region_variant&intron_variant | LOW | c.69-6T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695213 | ||||||
chr1:58695310
|
ATACT | A | 132 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(129): Show | 140 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.69-107_69-104delAG others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695310 | ||||||
chr1:58695313
|
C | G | 1 | a0002c0002t0002g0088 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.69-106G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695313 | ||||||
chr1:58695461
|
G | A | 4 | a0004c0004t0007g0026a0004c0004t0007g0322a0004c0004t0007g0323others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-254C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695461 | ||||||
chr1:58695597
|
A | G | 3 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0014g0054 | 3 | HG00438.hp1 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.69-390T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695597 | ||||||
chr1:58695643
|
C | A | 16 | a0001c0001t0001g0020a0001c0001t0001g0183a0001c0001t0001g0196others(13): Show | 17 | HG00597.hp1 HG02040.hp1 NA18939.hp2 others(14): Show |
intron_variant | MODIFIER | c.69-436G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695643 | ||||||
chr1:58695660
|
G | GA | 117 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(114): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.69-454dupT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695660 | ||||||
chr1:58695663
|
A | T | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-456T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695663 | ||||||
chr1:58695836
|
G | T | 340 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(337): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.69-629C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695836 | ||||||
chr1:58695907
|
T | C | 7 | a0002c0005t0006g0252a0002c0005t0016g0254a0002c0005t0016g0255others(4): Show | 7 | HG00738.hp2 HG00741.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-700A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58695907 | ||||||
chr1:58696006
|
C | A | 37 | a0002c0005t0006g0234a0002c0005t0006g0235a0002c0005t0006g0236others(34): Show | 40 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.69-799G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696006 | ||||||
chr1:58696039
|
C | G | 1 | a0003c0003t0022g0284 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.69-832G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696039 | ||||||
chr1:58696078
|
T | C | 1 | a0001c0001t0054g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.69-871A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696078 | ||||||
chr1:58696083
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.69-876A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696083 | ||||||
chr1:58696250
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.69-1043G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696250 | ||||||
chr1:58696268
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-1061A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696268 | ||||||
chr1:58696277
|
A | G | 363 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(360): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.69-1070T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696277 | ||||||
chr1:58696434
|
T | C | 341 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(338): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.69-1227A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696434 | ||||||
chr1:58696476
|
T | C | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.69-1269A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696476 | ||||||
chr1:58696674
|
C | G | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-1467G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696674 | ||||||
chr1:58696821
|
A | C | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.69-1614T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696821 | ||||||
chr1:58696858
|
C | T | 2 | a0002c0002t0002g0055a0002c0002t0014g0054 | 2 | HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.69-1651G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58696858 | ||||||
chr1:58697003
|
G | A | 152 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(149): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.69-1796C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697003 | ||||||
chr1:58697024
|
G | T | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-1817C>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697024 | ||||||
chr1:58697121
|
A | G | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.69-1914T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697121 | ||||||
chr1:58697251
|
G | GAGGC | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.69-2045_69-2044ins others(4): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697251 | ||||||
chr1:58697314
|
T | C | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-2107A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697314 | ||||||
chr1:58697349
|
TAAG | T | 37 | a0002c0005t0006g0234a0002c0005t0006g0235a0002c0005t0006g0236others(34): Show | 40 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.69-2145_69-2143del others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697349 | ||||||
chr1:58697392
|
C | T | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-2185G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697392 | ||||||
chr1:58697489
|
A | C | 2 | a0002c0002t0044g0006a0002c0002t0077g0046 | 3 | HG01891.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.69-2282T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697489 | ||||||
chr1:58697537
|
T | G | 1 | a0002c0002t0005g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.69-2330A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697537 | ||||||
chr1:58697582
|
CA | C | 8 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(5): Show | 8 | HG01517.hp2 NA18953.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.69-2376delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697582 | ||||||
chr1:58697591
|
A | T | 36 | a0002c0005t0006g0234a0002c0005t0006g0235a0002c0005t0006g0236others(33): Show | 39 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.69-2384T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697591 | ||||||
chr1:58697591
|
AT | A | 7 | a0001c0001t0001g0162a0001c0001t0001g0229a0001c0001t0004g0222others(4): Show | 7 | HG01952.hp2 HG02004.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-2385delA | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697591 | ||||||
chr1:58697614
|
C | A | 152 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(149): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.68+2371G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697614 | ||||||
chr1:58697651
|
G | A | 19 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(16): Show | 20 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.68+2334C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697651 | ||||||
chr1:58697736
|
G | C | 145 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(142): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.68+2249C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697736 | ||||||
chr1:58697769
|
A | G | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.68+2216T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697769 | ||||||
chr1:58697790
|
T | C | 2 | a0001c0001t0037g0273a0001c0001t0037g0275 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.68+2195A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697790 | ||||||
chr1:58697832
|
G | A | 5 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(2): Show | 5 | NA18953.hp2 NA18954.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+2153C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697832 | ||||||
chr1:58697835
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.68+2150G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697835 | ||||||
chr1:58697868
|
C | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(115): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.68+2117G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697868 | ||||||
chr1:58697881
|
A | G | 152 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(149): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.68+2104T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58697881 | ||||||
chr1:58698001
|
T | G | 7 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+1984A>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698001 | ||||||
chr1:58698045
|
C | T | 145 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(142): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.68+1940G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698045 | ||||||
chr1:58698084
|
C | CTATATAT others(13): Show |
5 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(2): Show | 5 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTATATAT others(15): Show |
2 | a0004c0004t0012g0369a0004c0004t0012g0370 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(22): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTATATAT others(21): Show |
2 | a0004c0004t0020g0350a0004c0004t0070g0351 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTATATAT others(23): Show |
1 | a0004c0004t0020g0346 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(30): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTATATAT others(31): Show |
2 | a0004c0004t0020g0347a0004c0004t0023g0348 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.68+1900_68+1901ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTCTATAT others(13): Show |
1 | a0004c0004t0040g0345 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTCTATAT others(19): Show |
1 | a0004c0004t0023g0325 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTCTATAT others(37): Show |
1 | a0004c0004t0020g0327 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
C | CTCTATAT others(49): Show |
1 | a0004c0004t0040g0352 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68+1900_68+1901ins others(56): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698084
|
CTA | C | 51 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(48): Show | 66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.68+1899_68+1900del others(2): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698084 | ||||||
chr1:58698086
|
A | C | 17 | a0003c0003t0003g0276a0003c0003t0003g0278a0003c0003t0003g0328others(14): Show | 17 | HG00639.hp2 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+1899T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698086 | ||||||
chr1:58698088
|
A | C | 51 | a0003c0003t0003g0001a0003c0003t0003g0004a0003c0003t0003g0027others(48): Show | 66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.68+1897T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698088 | ||||||
chr1:58698098
|
A | ATTTTTTT others(7): Show |
2 | a0002c0002t0045g0038a0002c0002t0045g0039 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68+1886_68+1887ins others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698098 | ||||||
chr1:58698099
|
TA | T | 8 | a0003c0003t0003g0276a0003c0003t0003g0278a0003c0003t0082g0279others(5): Show | 8 | HG01074.hp2 HG01081.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1885delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698099 | ||||||
chr1:58698099
|
TATA | T | 4 | a0003c0003t0003g0328a0003c0003t0003g0330a0003c0003t0011g0329others(1): Show | 4 | HG03041.hp1 NA18986.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1883_68+1885del others(3): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698099 | ||||||
chr1:58698100
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0019g0270 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.68+1884_68+1885ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | ||||||
chr1:58698100
|
A | ATTTTTTT others(5): Show |
2 | a0002c0005t0027g0021a0002c0005t0029g0356 | 3 | HG02280.hp1 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68+1884_68+1885ins others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | ||||||
chr1:58698100
|
A | ATTTTTTT others(9): Show |
1 | a0002c0002t0078g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68+1884_68+1885ins others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | ||||||
chr1:58698100
|
A | T | 2 | a0002c0002t0045g0038a0002c0002t0045g0039 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68+1885T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698100 | ||||||
chr1:58698101
|
TA | T | 3 | a0003c0003t0010g0333a0003c0003t0035g0332a0003c0003t0035g0334 | 3 | HG01099.hp1 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.68+1883delT | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698101 | ||||||
chr1:58698102
|
A | ATATATAT others(16): Show |
1 | a0005c0006t0011g0363 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(22): Show |
1 | a0004c0004t0007g0335 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0037g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(52): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(46): Show |
1 | a0002c0005t0080g0248 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(53): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(41): Show |
1 | a0002c0005t0006g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(48): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(42): Show |
1 | a0002c0005t0016g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(49): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0054g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(46): Show |
1 | a0006c0007t0025g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(53): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(39): Show |
1 | a0002c0002t0041g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(46): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(31): Show |
1 | a0006c0010t0010g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(36): Show |
2 | a0002c0005t0006g0246a0002c0005t0015g0247 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(37): Show |
1 | a0002c0002t0014g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(39): Show |
1 | a0002c0002t0002g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(46): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(41): Show |
2 | a0002c0002t0005g0099a0006c0007t0025g0048 | 2 | HG01934.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(48): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(42): Show |
1 | a0002c0002t0002g0077 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(49): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(31): Show |
1 | a0002c0005t0006g0262 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(32): Show |
1 | a0002c0005t0030g0258 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(35): Show |
1 | a0002c0002t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(36): Show |
1 | a0002c0002t0005g0124 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(38): Show |
1 | a0002c0002t0002g0110 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(45): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0037g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(31): Show |
1 | a0002c0005t0030g0250 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(32): Show |
4 | a0002c0005t0006g0242a0002c0005t0006g0245a0002c0005t0015g0243others(1): Show | 4 | NA18954.hp2 NA18965.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(33): Show |
2 | a0002c0005t0015g0239a0002c0005t0030g0238 | 2 | NA18999.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(40): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(34): Show |
2 | a0002c0002t0002g0123a0004c0004t0024g0031 | 2 | HG02615.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(41): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(35): Show |
1 | a0002c0002t0002g0114 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(36): Show |
3 | a0002c0002t0002g0107a0002c0002t0002g0109a0002c0002t0013g0108 | 3 | HG01981.hp2 NA19058.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(37): Show |
3 | a0002c0002t0002g0096a0002c0002t0002g0097a0002c0002t0002g0098 | 3 | HG01928.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(19): Show |
2 | a0005c0006t0011g0361a0005c0006t0026g0362 | 2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(34): Show |
2 | a0001c0001t0019g0269a0001c0001t0019g0271 | 2 | NA18953.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(41): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(22): Show |
2 | a0004c0004t0023g0272a0005c0006t0011g0360 | 2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(24): Show |
1 | a0005c0008t0010g0005 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(29): Show |
1 | a0004c0004t0071g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(30): Show |
1 | a0002c0005t0015g0241 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(32): Show |
1 | a0002c0002t0002g0122 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(33): Show |
1 | a0002c0002t0028g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(40): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(34): Show |
1 | a0002c0002t0002g0106 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(41): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(35): Show |
5 | a0002c0002t0002g0091a0002c0002t0002g0093a0002c0002t0002g0094others(2): Show | 5 | NA18939.hp1 NA18940.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(36): Show |
1 | a0002c0002t0005g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(43): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(37): Show |
2 | a0002c0002t0002g0062a0002c0002t0002g0063 | 2 | HG02148.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(44): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(38): Show |
1 | a0002c0002t0002g0052 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(45): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(17): Show |
1 | a0004c0004t0072g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0019g0268 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(25): Show |
2 | a0001c0001t0009g0230a0002c0005t0006g0261 | 2 | HG00099.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(32): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(28): Show |
1 | a0002c0005t0006g0240 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(29): Show |
1 | a0004c0004t0024g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(30): Show |
1 | a0002c0002t0002g0009 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(31): Show |
1 | a0002c0002t0002g0112 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(32): Show |
1 | a0002c0002t0005g0105 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(39): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0056g0267 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(20): Show |
2 | a0005c0006t0003g0359a0005c0006t0011g0358 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(23): Show |
1 | a0002c0005t0016g0260 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(30): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(24): Show |
3 | a0001c0001t0001g0223a0002c0005t0006g0256a0002c0005t0016g0257 | 3 | HG00140.hp2 HG01515.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(27): Show |
2 | a0002c0002t0002g0127a0002c0002t0002g0128 | 2 | HG03942.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(28): Show |
9 | a0002c0002t0002g0008a0002c0002t0002g0119a0002c0002t0005g0116others(6): Show | 10 | HG03654.hp1 HG03704.hp2 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(29): Show |
2 | a0002c0002t0014g0111a0004c0004t0024g0030 | 2 | HG02055.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(30): Show |
2 | a0002c0002t0002g0103a0002c0002t0002g0104 | 2 | HG01070.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(31): Show |
3 | a0002c0002t0002g0088a0002c0002t0028g0089a0002c0002t0028g0090 | 3 | HG02083.hp1 HG02129.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(38): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(33): Show |
2 | a0002c0002t0002g0061a0002c0002t0005g0060 | 2 | HG02027.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(40): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(20): Show |
1 | a0002c0005t0006g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(22): Show |
2 | a0002c0005t0016g0254a0002c0005t0016g0255 | 2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(24): Show |
1 | a0002c0002t0005g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(25): Show |
1 | a0002c0005t0006g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(32): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(27): Show |
1 | a0004c0004t0066g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(28): Show |
2 | a0002c0002t0002g0101a0002c0002t0014g0102 | 2 | HG01346.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(29): Show |
4 | a0002c0002t0002g0086a0002c0002t0002g0087a0002c0002t0005g0085others(1): Show | 4 | HG01884.hp1 NA18947.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(30): Show |
4 | a0002c0002t0005g0050a0002c0002t0005g0075a0002c0002t0083g0073others(1): Show | 4 | HG00544.hp2 HG00621.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(12): Show |
1 | a0002c0002t0013g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(19): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(20): Show |
6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 6 | HG01243.hp1 HG03927.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0050g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(24): Show |
1 | a0002c0005t0006g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(31): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(26): Show |
1 | a0002c0002t0002g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(33): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(27): Show |
8 | a0002c0002t0002g0078a0002c0002t0002g0079a0002c0002t0002g0083others(5): Show | 8 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(28): Show |
7 | a0002c0002t0002g0069a0002c0002t0002g0070a0002c0002t0002g0071others(4): Show | 8 | HG02055.hp2 NA18981.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(35): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(29): Show |
3 | a0002c0002t0002g0058a0002c0002t0014g0059a0002c0002t0074g0057 | 3 | HG01361.hp1 NA18946.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(36): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(30): Show |
1 | a0002c0002t0002g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(37): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(17): Show |
6 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0228others(3): Show | 6 | HG00140.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(18): Show |
12 | a0001c0001t0001g0020a0001c0001t0001g0206a0001c0001t0001g0207others(9): Show | 13 | HG02040.hp1 HG02738.hp2 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0205a0001c0001t0004g0204 | 4 | HG01891.hp1 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0004g0199a0001c0001t0008g0200a0001c0001t0008g0201 | 3 | HG01099.hp2 HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0009g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(29): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(26): Show |
1 | a0002c0002t0002g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(33): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(27): Show |
3 | a0002c0002t0002g0055a0002c0002t0002g0056a0002c0002t0014g0054 | 3 | HG00438.hp1 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(34): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0055g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(18): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(14): Show |
1 | a0002c0005t0079g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(21): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0004g0203 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(18): Show |
16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0188others(13): Show | 18 | HG00597.hp1 HG01070.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(19): Show |
9 | a0001c0001t0001g0016a0001c0001t0001g0176a0001c0001t0001g0180others(6): Show | 10 | HG00621.hp2 HG01934.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(20): Show |
4 | a0001c0001t0001g0164a0001c0001t0004g0166a0001c0001t0008g0163others(1): Show | 4 | HG01169.hp1 HG01257.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(21): Show |
1 | a0004c0004t0039g0355 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(35): Show |
1 | a0002c0005t0006g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(42): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(14): Show |
1 | a0002c0005t0006g0253 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(21): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0009g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(17): Show |
9 | a0001c0001t0001g0134a0001c0001t0001g0171a0001c0001t0001g0174others(6): Show | 9 | HG02129.hp2 HG02148.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(24): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(18): Show |
26 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(23): Show | 36 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(19): Show |
6 | a0001c0001t0001g0141a0001c0001t0004g0138a0001c0001t0004g0140others(3): Show | 6 | HG01978.hp2 HG02004.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0009g0137 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(27): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(21): Show |
1 | a0004c0004t0063g0353 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0036g0036a0001c0001t0053g0043 | 2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(18): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(13): Show |
2 | a0004c0004t0026g0033a0004c0004t0026g0034 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(20): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(15): Show |
2 | a0002c0002t0002g0125a0002c0002t0013g0126 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(22): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0004g0136a0001c0001t0009g0357 | 2 | HG02258.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(26): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(21): Show |
1 | a0002c0002t0042g0053 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(28): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0036g0044a0001c0001t0057g0042 | 2 | HG01192.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(17): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATAT others(18): Show |
1 | a0002c0002t0002g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(25): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATATTT others(9): Show |
1 | a0002c0005t0006g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(16): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATATTTTT others(6): Show |
3 | a0002c0005t0006g0252a0002c0005t0027g0251a0002c0005t0043g0023 | 4 | HG01074.hp1 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1882_68+1883ins others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATTTTTTT others(5): Show |
1 | a0002c0005t0029g0022 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68+1871_68+1882dup others(12): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATTTTTTT others(7): Show |
1 | a0002c0002t0044g0006 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.68+1869_68+1882dup others(14): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATTTTTTT others(11): Show |
1 | a0002c0002t0077g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(18): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | ATTTTTTT others(12): Show |
1 | a0002c0002t0002g0064 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.68+1882_68+1883ins others(19): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698102
|
A | T | 63 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0078g0040others(60): Show | 78 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.68+1883T>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698102 | ||||||
chr1:58698103
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.68+1881_68+1882ins others(13): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698103 | ||||||
chr1:58698103
|
T | TATATATA others(16): Show |
1 | a0004c0004t0003g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.68+1881_68+1882ins others(23): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698103 | ||||||
chr1:58698104
|
T | A | 9 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(6): Show | 9 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.68+1881A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698104 | ||||||
chr1:58698105
|
T | A | 1 | a0001c0001t0019g0271 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.68+1880A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698105 | ||||||
chr1:58698315
|
T | C | 1 | a0001c0001t0036g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.68+1670A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698315 | ||||||
chr1:58698351
|
C | T | 1 | a0002c0002t0005g0050 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.68+1634G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698351 | ||||||
chr1:58698468
|
A | G | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.68+1517T>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698468 | ||||||
chr1:58698515
|
C | G | 1 | a0004c0004t0023g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68+1470G>C | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698515 | ||||||
chr1:58698548
|
A | AG | 140 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(137): Show | 148 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.68+1436dupC | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698548 | ||||||
chr1:58698572
|
A | AAAAATT | 145 | a0001c0001t0019g0268a0001c0001t0019g0269a0001c0001t0019g0270others(142): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.68+1412_68+1413ins others(6): Show |
MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698572 | ||||||
chr1:58698585
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.68+1400A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698585 | ||||||
chr1:58698741
|
T | C | 7 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(4): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1244A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698741 | ||||||
chr1:58698797
|
T | A | 1 | a0004c0004t0040g0352 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68+1188A>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698797 | ||||||
chr1:58698825
|
C | A | 4 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0076g0049others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1160G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698825 | ||||||
chr1:58698840
|
C | T | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(130): Show | 141 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.68+1145G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698840 | ||||||
chr1:58698855
|
T | C | 87 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0051others(84): Show | 91 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.68+1130A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698855 | ||||||
chr1:58698911
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(114): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.68+1074G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58698911 | ||||||
chr1:58699038
|
T | C | 3 | a0004c0004t0039g0354a0004c0004t0039g0355a0004c0004t0063g0353 | 3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.68+947A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699038 | ||||||
chr1:58699047
|
A | C | 1 | a0003c0003t0003g0135 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68+938T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699047 | ||||||
chr1:58699178
|
G | C | 1 | a0004c0004t0072g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+807C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699178 | ||||||
chr1:58699320
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.68+665C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699320 | ||||||
chr1:58699370
|
A | C | 98 | a0001c0001t0001g0133a0001c0001t0001g0134a0002c0002t0002g0008others(95): Show | 103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.68+615T>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699370 | ||||||
chr1:58699528
|
C | T | 4 | a0001c0001t0036g0036a0001c0001t0036g0044a0001c0001t0053g0043others(1): Show | 4 | HG01192.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+457G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699528 | ||||||
chr1:58699593
|
C | T | 1 | a0001c0001t0008g0041 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.68+392G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699593 | ||||||
chr1:58699616
|
C | T | 3 | a0002c0002t0045g0038a0002c0002t0045g0039a0002c0002t0078g0040 | 3 | HG02723.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68+369G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699616 | ||||||
chr1:58699697
|
G | C | 1 | a0002c0005t0029g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68+288C>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699697 | ||||||
chr1:58699727
|
T | C | 1 | a0001c0001t0009g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68+258A>G | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699727 | ||||||
chr1:58699829
|
C | A | 7 | a0005c0006t0003g0359a0005c0006t0011g0358a0005c0006t0011g0360others(4): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+156G>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699829 | ||||||
chr1:58699836
|
C | T | 1 | a0004c0004t0072g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+149G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699836 | ||||||
chr1:58699871
|
C | T | 1 | a0001c0001t0036g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68+114G>A | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699871 | ||||||
chr1:58699923
|
G | A | 7 | a0004c0004t0012g0365a0004c0004t0012g0366a0004c0004t0012g0367others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+62C>T | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699923 | ||||||
chr1:58699944
|
TC | T | 7 | a0004c0004t0024g0030a0004c0004t0024g0031a0004c0004t0024g0032others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+40delG | MYSM1 | ENSG00000162601.12 | transcript | ENST00000472487.6 | protein_coding | 1/19 | chr1 | 58699944 |