geneid | 23209 |
---|---|
ensemblid | ENSG00000100427.16 |
hgncid | 17082 |
symbol | MLC1 |
name | modulator of VRAC current 1 |
refseq_nuc | NM_015166.4 |
refseq_prot | NP_055981.1 |
ensembl_nuc | ENST00000311597.10 |
ensembl_prot | ENSP00000310375.6 |
mane_status | MANE Select |
chr | chr22 |
start | 50059391 |
end | 50085426 |
strand | - |
ver | v1.2 |
region | chr22:50059391-50085426 |
region5000 | chr22:50054391-50090426 |
regionname0 | MLC1_chr22_50059391_50085426 |
regionname5000 | MLC1_chr22_50054391_50090426 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 377 | 202 | 46 | 45 | 85 | 8 | 16 | 62 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0002 | 0/0 | 388 | 4 | 0 | 2 | 1 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0003 | 0/0 | 377 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0004 | 0/0 | 377 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0005 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0006 | 0/0 | 369 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1134 | 198 | 45 | 44 | 84 | 8 | 15 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0002 | 0/0 | 1167 | 4 | 0 | 2 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0003 | 0/0 | 1134 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0004 | 0/0 | 1134 | 2 | 1 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0005 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0006 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0007 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0008 | 0/0 | 1166 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0009 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
c0010 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2324 | 93 | 30 | 7 | 47 | 1 | 6 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0002 | 0/0 | 2324 | 49 | 0 | 9 | 33 | 3 | 4 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0003 | 0/0 | 2324 | 14 | 1 | 9 | 0 | 1 | 3 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0004 | 0/0 | 2324 | 9 | 0 | 4 | 1 | 2 | 2 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0005 | 0/0 | 2324 | 7 | 6 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0006 | 0/0 | 2324 | 7 | 1 | 5 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0007 | 0/0 | 2230 | 5 | 0 | 2 | 1 | 0 | 2 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0008 | 0/0 | 2324 | 4 | 0 | 3 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0009 | 0/0 | 2273 | 4 | 3 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0010 | 0/0 | 2275 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0011 | 0/0 | 2324 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0012 | 0/0 | 2273 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0013 | 0/0 | 2273 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0014 | 0/0 | 2273 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0015 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0016 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0017 | 0/0 | 2324 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0018 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0019 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0020 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0021 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0022 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0023 | 0/0 | 2324 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0024 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
t0025 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1134 | 198 | 45 | 44 | 84 | 8 | 15 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0005 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0007 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0009 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0010 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0002c0002 | 0/0 | 1167 | 4 | 0 | 2 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0003c0003 | 0/0 | 1134 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0004c0004 | 0/0 | 1134 | 2 | 1 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0005c0006 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0006c0008 | 0/0 | 1166 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3457 | 89 | 29 | 6 | 46 | 1 | 5 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0002 | 0/0 | 3457 | 48 | 0 | 9 | 32 | 3 | 4 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0003 | 0/0 | 3457 | 14 | 1 | 9 | 0 | 1 | 3 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0004 | 0/0 | 3457 | 8 | 0 | 4 | 0 | 2 | 2 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0005 | 0/0 | 3457 | 7 | 6 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0006 | 0/0 | 3457 | 7 | 1 | 5 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0008 | 0/0 | 3457 | 4 | 0 | 3 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0009 | 0/0 | 3406 | 4 | 3 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0010 | 0/0 | 3408 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0011 | 0/0 | 3457 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0012 | 0/0 | 3406 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0013 | 0/0 | 3406 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0015 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0016 | 0/0 | 3407 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0017 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0018 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0019 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0020 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0021 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0023 | 0/0 | 3457 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0024 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0001t0025 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0005t0013 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0007t0001 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0009t0014 | 0/0 | 3406 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0001c0010t0001 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0002c0002t0007 | 0/0 | 3396 | 4 | 0 | 2 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0003c0003t0001 | 0/0 | 3457 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0004c0004t0004 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0004c0004t0022 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0005c0006t0002 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
a0006c0008t0007 | 0/0 | 3395 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | copy fasta | chr22 | 50054391 | 50090426 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0005g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0005g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0008g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0009g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0010g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0012g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0013g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0016g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0017g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0018g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0021g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0023g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0024g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0001t0025g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0005t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0007t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0009t0014g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0001c0010t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0002c0002t0007g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0002c0002t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0002c0002t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0002c0002t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0004c0004t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0004c0004t0022g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0005c0006t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
a0006c0008t0007g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0056 | EUR | GBR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00438 | hp2 | a0001 | c0001 | t0020 | g0021 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00621 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00673 | hp1 | a0002 | c0002 | t0007 | g0168 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0116 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0068 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0029 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0061 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0089 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01256 | hp2 | a0001 | c0001 | t0023 | g0098 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01346 | hp1 | a0001 | c0001 | t0008 | g0055 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01358 | hp1 | a0002 | c0002 | t0007 | g0167 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0111 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01496 | hp2 | a0001 | c0009 | t0014 | g0105 | AMR | CLM | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01515 | hp1 | a0001 | c0001 | t0017 | g0109 | EUR | IBS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0180 | EUR | IBS | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0118 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02004 | hp1 | a0002 | c0002 | t0007 | g0166 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02004 | hp2 | a0001 | c0001 | t0010 | g0014 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02074 | hp1 | a0001 | c0001 | t0019 | g0091 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02148 | hp2 | a0001 | c0001 | t0012 | g0108 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02257 | hp1 | a0001 | c0001 | t0025 | g0190 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02273 | hp1 | a0001 | c0001 | t0010 | g0014 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PEL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02622 | hp2 | a0001 | c0005 | t0013 | g0064 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02965 | hp1 | a0001 | c0001 | t0018 | g0082 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03239 | hp1 | a0001 | c0001 | t0008 | g0049 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0183 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03688 | hp1 | a0002 | c0002 | t0007 | g0165 | SAS | STU | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03688 | hp2 | a0001 | c0010 | t0001 | g0135 | SAS | STU | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03831 | hp1 | a0006 | c0008 | t0007 | g0119 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | YRI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18967 | hp2 | a0001 | c0001 | t0015 | g0020 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18978 | hp1 | a0001 | c0001 | t0024 | g0146 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19043 | hp1 | a0001 | c0001 | t0021 | g0189 | AFR | LWK | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19065 | hp1 | a0001 | c0007 | t0001 | g0054 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19074 | hp1 | a0005 | c0006 | t0002 | g0157 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19087 | hp1 | a0004 | c0004 | t0004 | g0164 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA19090 | hp2 | a0001 | c0001 | t0016 | g0107 | EAS | JPT | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | ASW | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0170 | EUR | TSI | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0081 | AFR | ACB | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
HG03471 | hp2 | a0004 | c0004 | t0022 | g0163 | AFR | MSL | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | USA | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0101 | REF | REF | MLC1_chr22_50054391_50090426 | MLC1 | chr22 | 50054391 | 50090426 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50061603
|
C | T | 1 | a0005 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.1114G>A | p.Val372Met | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1245/3457 | 1114/1134 | 372/377 | chr22 | 50061603 | ||
chr22:50064040
|
A | AGCACCCC others(25): Show |
1 | a0006 | 1 | HG03831.hp1 | frameshift_variant | HIGH | c.1052_1053insCGGGGA others(26): Show |
p.Ala355fs | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1183/3457 | 1052/1134 | 351/377 | chr22 | 50064040 | ||
chr22:50064040
|
A | AGCACCCC others(26): Show |
1 | a0002 | 4 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.1052_1053insCGGGGA others(27): Show |
p.Ala351_Gly352insGl others(31): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1183/3457 | 1052/1134 | 351/377 | chr22 | 50064040 | ||
chr22:50064062
|
T | C | 2 | a0002a0006 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
missense_variant | MODERATE | c.1031A>G | p.Asn344Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1162/3457 | 1031/1134 | 344/377 | chr22 | 50064062 | ||
chr22:50064161
|
A | T | 1 | a0003 | 2 | HG01109.hp1 HG02630.hp1 |
missense_variant | MODERATE | c.932T>A | p.Val311Glu | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1063/3457 | 932/1134 | 311/377 | chr22 | 50064161 | ||
chr22:50077414
|
C | A | 2 | a0002a0004 | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
missense_variant | MODERATE | c.512G>T | p.Cys171Phe | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/12 | 643/3457 | 512/1134 | 171/377 | chr22 | 50077414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50064088
|
C | A | 1 | a0001c0007 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.1005G>T | p.Leu335Leu | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1136/3457 | 1005/1134 | 335/377 | chr22 | 50064088 | ||
chr22:50064097
|
A | G | 2 | a0002c0002a0006c0008 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.996T>C | p.Ser332Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1127/3457 | 996/1134 | 332/377 | chr22 | 50064097 | ||
chr22:50064115
|
G | A | 2 | a0002c0002a0006c0008 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.978C>T | p.Cys326Cys | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/12 | 1109/3457 | 978/1134 | 326/377 | chr22 | 50064115 | ||
chr22:50076841
|
T | C | 3 | a0001c0009a0002c0002a0004c0004 | 7 | HG00673.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.597A>G | p.Ser199Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/12 | 728/3457 | 597/1134 | 199/377 | chr22 | 50076841 | ||
chr22:50076844
|
G | A | 3 | a0001c0009a0002c0002a0004c0004 | 7 | HG00673.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
synonymous_variant | LOW | c.594C>T | p.Tyr198Tyr | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/12 | 725/3457 | 594/1134 | 198/377 | chr22 | 50076844 | ||
chr22:50076895
|
G | A | 1 | a0001c0010 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.543C>T | p.Ser181Ser | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/12 | 674/3457 | 543/1134 | 181/377 | chr22 | 50076895 | ||
chr22:50083135
|
C | T | 1 | a0001c0005 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.216G>A | p.Leu72Leu | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/12 | 347/3457 | 216/1134 | 72/377 | chr22 | 50083135 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50059532
|
C | T | 1 | a0001c0001t0024 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 2051 | chr22 | 50059532 | |||||
chr22:50059533
|
G | A | 1 | a0001c0001t0018 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 2050 | chr22 | 50059533 | |||||
chr22:50059601
|
G | GC | 4 | a0001c0001t0010a0001c0001t0019a0002c0002t0007others(1): Show | 8 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1981dupG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1981 | chr22 | 50059601 | |||||
chr22:50059620
|
G | C | 2 | a0001c0001t0008a0001c0001t0017 | 5 | HG01175.hp1 HG01192.hp2 HG01346.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1963C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1963 | chr22 | 50059620 | |||||
chr22:50059747
|
C | T | 1 | a0001c0001t0012 | 2 | HG00733.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1836G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1836 | chr22 | 50059747 | |||||
chr22:50059819
|
C | A | 2 | a0001c0001t0004a0004c0004t0004 | 9 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1764G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1764 | chr22 | 50059819 | |||||
chr22:50059894
|
A | C | 1 | a0001c0001t0011 | 2 | HG02486.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1689T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1689 | chr22 | 50059894 | |||||
chr22:50059960
|
C | A | 4 | a0001c0001t0009a0001c0001t0012a0001c0001t0013others(1): Show | 8 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1623G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1623 | chr22 | 50059960 | |||||
chr22:50060214
|
A | AT | 2 | a0001c0001t0010a0001c0001t0016 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1368dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1368 | chr22 | 50060214 | |||||
chr22:50060249
|
C | T | 2 | a0001c0001t0010a0001c0001t0016 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1334G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1334 | chr22 | 50060249 | |||||
chr22:50060262
|
T | C | 1 | a0001c0009t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1321A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1321 | chr22 | 50060262 | |||||
chr22:50060440
|
G | A | 3 | a0001c0001t0010a0001c0001t0016a0001c0009t0014 | 4 | HG01496.hp2 HG02004.hp2 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1143C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1143 | chr22 | 50060440 | |||||
chr22:50060456
|
G | A | 3 | a0001c0001t0003a0001c0001t0004a0004c0004t0004 | 23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1127C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 1127 | chr22 | 50060456 | |||||
chr22:50060592
|
A | C | 2 | a0002c0002t0007a0006c0008t0007 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*991T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 991 | chr22 | 50060592 | |||||
chr22:50060613
|
C | G | 2 | a0001c0001t0010a0001c0001t0016 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*970G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 970 | chr22 | 50060613 | |||||
chr22:50060646
|
G | A | 2 | a0002c0002t0007a0006c0008t0007 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 937 | chr22 | 50060646 | |||||
chr22:50060697
|
AGCAGCGG others(95): Show |
A | 2 | a0002c0002t0007a0006c0008t0007 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*784_*885del | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 784 | chr22 | 50060697 | |||||
chr22:50060736
|
G | T | 1 | a0001c0001t0017 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 847 | chr22 | 50060736 | |||||
chr22:50060759
|
TGTGGCAC others(44): Show |
T | 7 | a0001c0001t0009a0001c0001t0010a0001c0001t0012others(4): Show | 12 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*773_*823delGTGGCC others(45): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 773 | chr22 | 50060759 | |||||
chr22:50060910
|
C | T | 1 | a0001c0001t0021 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*673G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 673 | chr22 | 50060910 | |||||
chr22:50060922
|
C | G | 1 | a0001c0001t0009 | 4 | HG01255.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*661G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 661 | chr22 | 50060922 | |||||
chr22:50061011
|
G | A | 1 | a0001c0009t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 572 | chr22 | 50061011 | |||||
chr22:50061031
|
A | T | 1 | a0001c0001t0015 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 552 | chr22 | 50061031 | |||||
chr22:50061063
|
G | A | 1 | a0001c0001t0020 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 520 | chr22 | 50061063 | |||||
chr22:50061152
|
G | A | 2 | a0001c0001t0021a0004c0004t0022 | 2 | HG03471.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*431C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 431 | chr22 | 50061152 | |||||
chr22:50061169
|
G | A | 1 | a0001c0001t0006 | 7 | HG00621.hp1 HG01358.hp2 HG01975.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 414 | chr22 | 50061169 | |||||
chr22:50061205
|
T | TGACCCCC | 2 | a0002c0002t0007a0006c0008t0007 | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*377_*378insGGGGGT others(1): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 377 | chr22 | 50061205 | |||||
chr22:50061244
|
G | A | 1 | a0001c0001t0005 | 7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 339 | chr22 | 50061244 | |||||
chr22:50061528
|
G | A | 1 | a0001c0001t0023 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 55 | chr22 | 50061528 | |||||
chr22:50061535
|
T | C | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0024others(3): Show | 62 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*48A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 48 | chr22 | 50061535 | |||||
chr22:50061538
|
T | C | 4 | a0001c0001t0009a0001c0001t0012a0001c0001t0013others(1): Show | 8 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 45 | chr22 | 50061538 | |||||
chr22:50061571
|
C | T | 1 | a0001c0009t0014 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 12/12 | 12 | chr22 | 50061571 | |||||
chr22:50085395
|
T | C | 1 | a0001c0001t0025 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/12 | 493 | chr22 | 50085395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50061834
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-177A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061834 | ||||||
chr22:50061868
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1060-211G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061868 | ||||||
chr22:50061872
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1060-215G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061872 | ||||||
chr22:50061928
|
G | C | 1 | a0001c0001t0010g0014 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1060-271C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061928 | ||||||
chr22:50061938
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1060-281G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061938 | ||||||
chr22:50061946
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0015g0020 | 2 | NA18967.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1060-289C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50061946 | ||||||
chr22:50062046
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0084a0001c0001t0001g0086 | 4 | HG02965.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-389C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062046 | ||||||
chr22:50062098
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-441A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062098 | ||||||
chr22:50062125
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-468G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062125 | ||||||
chr22:50062171
|
A | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-514T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062171 | ||||||
chr22:50062172
|
C | T | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1060-515G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062172 | ||||||
chr22:50062176
|
A | AAGCCCCA others(13): Show |
2 | a0001c0001t0001g0023a0001c0001t0015g0020 | 2 | NA18967.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1060-539_1060-520d others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062176 | ||||||
chr22:50062176
|
A | G | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1060-519T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062176 | ||||||
chr22:50062187
|
ATCCACCC others(13): Show |
A | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-550_1060-531d others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062187 | ||||||
chr22:50062188
|
T | TCCACCCT others(13): Show |
1 | a0004c0004t0022g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1060-532_1060-531i others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062188 | ||||||
chr22:50062188
|
T | TCCACCCT others(33): Show |
1 | a0001c0001t0021g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060-532_1060-531i others(42): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062188 | ||||||
chr22:50062208
|
T | C | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(150): Show | 170 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1060-551A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062208 | ||||||
chr22:50062208
|
T | TCCACCCT others(121): Show |
18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0084others(15): Show | 20 | HG00544.hp1 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1060-552_1060-551i others(130): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062208 | ||||||
chr22:50062222
|
C | CAGCCGCC others(33): Show |
5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-566_1060-565i others(42): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062222 | ||||||
chr22:50062244
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-587T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062244 | ||||||
chr22:50062267
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-610T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062267 | ||||||
chr22:50062268
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1060-611G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062268 | ||||||
chr22:50062274
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-617A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062274 | ||||||
chr22:50062279
|
C | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 54 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1060-622G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062279 | ||||||
chr22:50062288
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-631A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062288 | ||||||
chr22:50062292
|
T | C | 6 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-635A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062292 | ||||||
chr22:50062292
|
TCCTGAGC others(13): Show |
T | 1 | a0001c0001t0002g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1060-655_1060-636d others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062292 | ||||||
chr22:50062522
|
AACAGCAG others(37): Show |
A | 1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-909_1060-866d others(46): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062522 | ||||||
chr22:50062615
|
T | C | 1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-958A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062615 | ||||||
chr22:50062617
|
G | C | 1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-960C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062617 | ||||||
chr22:50062630
|
A | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(94): Show | 111 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1060-973T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062630 | ||||||
chr22:50062677
|
C | A | 1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-1020G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062677 | ||||||
chr22:50062678
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-1021T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062678 | ||||||
chr22:50062681
|
G | C | 1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1060-1024C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062681 | ||||||
chr22:50062708
|
A | G | 7 | a0001c0001t0010g0014a0001c0001t0016g0107a0002c0002t0007g0165others(4): Show | 8 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060-1051T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062708 | ||||||
chr22:50062791
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-1134G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062791 | ||||||
chr22:50062805
|
G | T | 1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-1148C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062805 | ||||||
chr22:50062810
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0041 | 2 | NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1060-1153G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062810 | ||||||
chr22:50062811
|
G | A | 1 | a0003c0003t0001g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1060-1154C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062811 | ||||||
chr22:50062845
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0149 | 2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1060-1188G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062845 | ||||||
chr22:50062852
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+1182G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062852 | ||||||
chr22:50062918
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1059+1116G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062918 | ||||||
chr22:50062975
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1059+1059C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50062975 | ||||||
chr22:50063056
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+978C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063056 | ||||||
chr22:50063111
|
A | AAGCGTTA others(7): Show |
1 | a0006c0008t0007g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+922_1059+923i others(16): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063111 | ||||||
chr22:50063115
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+919T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063115 | ||||||
chr22:50063157
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+877G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063157 | ||||||
chr22:50063201
|
G | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+833C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063201 | ||||||
chr22:50063256
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 191 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.1059+778A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063256 | ||||||
chr22:50063366
|
G | A | 1 | a0001c0001t0012g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1059+668C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063366 | ||||||
chr22:50063405
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+629C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063405 | ||||||
chr22:50063458
|
C | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+576G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063458 | ||||||
chr22:50063459
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+575A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063459 | ||||||
chr22:50063472
|
C | CA | 6 | a0001c0001t0001g0045a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | HG01496.hp2 NA18963.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+561dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063472 | ||||||
chr22:50063472
|
CA | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0083others(6): Show | 9 | HG01070.hp2 HG01256.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+561delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063472 | ||||||
chr22:50063472
|
CAAAAA | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+557_1059+561d others(7): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063472 | ||||||
chr22:50063490
|
A | AC | 1 | a0001c0001t0010g0014 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1059+543_1059+544i others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063490 | ||||||
chr22:50063490
|
A | C | 1 | a0001c0001t0016g0107 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1059+544T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063490 | ||||||
chr22:50063496
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+538C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063496 | ||||||
chr22:50063511
|
T | G | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1059+523A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063511 | ||||||
chr22:50063528
|
G | C | 21 | a0001c0001t0003g0004a0001c0001t0003g0169a0001c0001t0003g0170others(18): Show | 23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1059+506C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063528 | ||||||
chr22:50063587
|
C | A | 1 | a0001c0001t0004g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1059+447G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063587 | ||||||
chr22:50063621
|
G | GCAGGCCT others(60): Show |
1 | a0001c0001t0008g0029 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1059+346_1059+412d others(69): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063621 | ||||||
chr22:50063706
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+328A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063706 | ||||||
chr22:50063730
|
T | G | 1 | a0001c0001t0001g0023 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1059+304A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063730 | ||||||
chr22:50063742
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+292A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063742 | ||||||
chr22:50063743
|
G | GACCA | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+290_1059+291i others(6): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063743 | ||||||
chr22:50063772
|
T | TGGCTGGG others(94): Show |
2 | a0001c0001t0021g0189a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1059+261_1059+262i others(103): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063772 | ||||||
chr22:50063781
|
C | A | 2 | a0001c0001t0021g0189a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1059+253G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063781 | ||||||
chr22:50063781
|
C | CCCCCCAT others(226): Show |
1 | a0001c0001t0002g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1059+252_1059+253i others(235): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063781 | ||||||
chr22:50063786
|
A | ATGGGCCA others(223): Show |
1 | a0001c0001t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1059+247_1059+248i others(232): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | ||||||
chr22:50063786
|
A | ATGGGCCA others(222): Show |
1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+247_1059+248i others(231): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | ||||||
chr22:50063786
|
A | ATGGGCCA others(223): Show |
175 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 197 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.1059+247_1059+248i others(232): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | ||||||
chr22:50063786
|
A | ATGGGCCA others(224): Show |
1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1059+247_1059+248i others(233): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | ||||||
chr22:50063786
|
A | G | 8 | a0001c0001t0002g0144a0001c0001t0021g0189a0002c0002t0007g0165others(5): Show | 8 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+248T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063786 | ||||||
chr22:50063814
|
A | ACTGCAGG others(160): Show |
5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+219_1059+220i others(169): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063814 | ||||||
chr22:50063817
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+217C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063817 | ||||||
chr22:50063832
|
C | CCCCAGCT others(222): Show |
1 | a0001c0001t0001g0045 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1059+201_1059+202i others(231): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063832 | ||||||
chr22:50063836
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0004g0175a0001c0001t0004g0181 | 3 | HG01433.hp1 HG02486.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+198C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063836 | ||||||
chr22:50063856
|
T | C | 2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+178A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063856 | ||||||
chr22:50063872
|
A | G | 2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+162T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063872 | ||||||
chr22:50063878
|
T | A | 2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+156A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063878 | ||||||
chr22:50063882
|
C | CACAGGCT others(155): Show |
2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+151_1059+152i others(164): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063882 | ||||||
chr22:50063884
|
T | C | 2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+150A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063884 | ||||||
chr22:50063920
|
G | GGGCTACT others(28): Show |
2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1059+113_1059+114i others(37): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50063920 | ||||||
chr22:50064007
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+27A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50064007 | ||||||
chr22:50064018
|
C | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 55 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1059+16G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 11/11 | chr22 | 50064018 | ||||||
chr22:50064206
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA19056.hp1 | splice_region_variant&intron_variant | LOW | c.895-8G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064206 | ||||||
chr22:50064207
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-9C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064207 | ||||||
chr22:50064221
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-23C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064221 | ||||||
chr22:50064337
|
C | T | 12 | a0001c0001t0009g0011a0001c0001t0009g0078a0001c0001t0009g0088others(9): Show | 13 | HG00673.hp1 HG00733.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-139G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064337 | ||||||
chr22:50064383
|
T | C | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-185A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064383 | ||||||
chr22:50064457
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 89 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.895-259G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064457 | ||||||
chr22:50064459
|
T | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 55 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.895-261A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064459 | ||||||
chr22:50064464
|
A | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.895-266T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064464 | ||||||
chr22:50064492
|
C | G | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-294G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064492 | ||||||
chr22:50064571
|
G | A | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.895-373C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064571 | ||||||
chr22:50064622
|
G | A | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-424C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064622 | ||||||
chr22:50064632
|
GT | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-435delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064632 | ||||||
chr22:50064634
|
G | T | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.895-436C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064634 | ||||||
chr22:50064883
|
CA | C | 21 | a0001c0001t0003g0004a0001c0001t0003g0169a0001c0001t0003g0170others(18): Show | 23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.895-686delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064883 | ||||||
chr22:50064907
|
C | A | 6 | a0001c0001t0009g0011a0001c0001t0009g0078a0001c0001t0009g0088others(3): Show | 7 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-709G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064907 | ||||||
chr22:50064907
|
C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 58 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.895-709G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064907 | ||||||
chr22:50064930
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-732T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064930 | ||||||
chr22:50064949
|
C | CAG | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-753_895-752dup others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50064949 | ||||||
chr22:50065212
|
C | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.895-1014G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065212 | ||||||
chr22:50065215
|
G | A | 2 | a0001c0001t0021g0189a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.895-1017C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065215 | ||||||
chr22:50065368
|
C | CA | 6 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0009g0011others(3): Show | 7 | HG01255.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1171dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065368 | ||||||
chr22:50065368
|
CAA | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1172_895-1171d others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065368 | ||||||
chr22:50065411
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1213G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065411 | ||||||
chr22:50065635
|
A | G | 6 | a0001c0001t0009g0011a0001c0001t0009g0078a0001c0001t0009g0088others(3): Show | 7 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-1437T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065635 | ||||||
chr22:50065650
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1452G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065650 | ||||||
chr22:50065725
|
T | C | 2 | a0001c0001t0021g0189a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.895-1527A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065725 | ||||||
chr22:50065881
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1683G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065881 | ||||||
chr22:50065938
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.895-1740C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50065938 | ||||||
chr22:50066017
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 191 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.895-1819T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066017 | ||||||
chr22:50066058
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1860A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066058 | ||||||
chr22:50066078
|
TC | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-1881delG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066078 | ||||||
chr22:50066118
|
G | T | 1 | a0002c0002t0007g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.895-1920C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066118 | ||||||
chr22:50066208
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2010C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066208 | ||||||
chr22:50066242
|
T | C | 1 | a0004c0004t0022g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.895-2044A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066242 | ||||||
chr22:50066257
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 55 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.895-2059C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066257 | ||||||
chr22:50066274
|
G | A | 9 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0080others(6): Show | 12 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.895-2076C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066274 | ||||||
chr22:50066308
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2110C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066308 | ||||||
chr22:50066312
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2114T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066312 | ||||||
chr22:50066352
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+2081T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066352 | ||||||
chr22:50066375
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+2058A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066375 | ||||||
chr22:50066478
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+1955T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066478 | ||||||
chr22:50066524
|
T | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 191 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.894+1909A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066524 | ||||||
chr22:50066659
|
T | TA | 9 | a0001c0001t0001g0058a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 10 | HG01255.hp2 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.894+1773dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066659 | ||||||
chr22:50066702
|
T | C | 1 | a0001c0001t0003g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.894+1731A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066702 | ||||||
chr22:50066704
|
C | G | 21 | a0001c0001t0003g0004a0001c0001t0003g0169a0001c0001t0003g0170others(18): Show | 23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+1729G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066704 | ||||||
chr22:50066723
|
G | GA | 6 | a0001c0001t0002g0127a0001c0001t0002g0137a0001c0001t0002g0138others(3): Show | 6 | HG02148.hp1 NA18946.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.894+1709dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066723 | ||||||
chr22:50066754
|
GAGGAGCA others(8): Show |
G | 1 | a0001c0001t0001g0096 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.894+1664_894+1678d others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066754 | ||||||
chr22:50066858
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.894+1575A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066858 | ||||||
chr22:50066860
|
T | TA | 7 | a0001c0001t0002g0117a0001c0001t0009g0011a0001c0001t0009g0078others(4): Show | 8 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+1572dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066860 | ||||||
chr22:50066892
|
G | C | 7 | a0001c0001t0002g0117a0001c0001t0009g0011a0001c0001t0009g0078others(4): Show | 8 | HG00733.hp2 HG01255.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+1541C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066892 | ||||||
chr22:50066906
|
GC | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 53 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.894+1526delG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50066906 | ||||||
chr22:50067078
|
G | A | 2 | a0001c0001t0001g0062a0001c0009t0014g0105 | 2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.894+1355C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067078 | ||||||
chr22:50067155
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+1278T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067155 | ||||||
chr22:50067258
|
G | A | 1 | a0001c0001t0009g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.894+1175C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067258 | ||||||
chr22:50067390
|
A | G | 21 | a0001c0001t0003g0004a0001c0001t0003g0169a0001c0001t0003g0170others(18): Show | 23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+1043T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067390 | ||||||
chr22:50067430
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+1003A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067430 | ||||||
chr22:50067446
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.894+987G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067446 | ||||||
chr22:50067454
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+979C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067454 | ||||||
chr22:50067478
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+955T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067478 | ||||||
chr22:50067493
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+940A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067493 | ||||||
chr22:50067495
|
T | TC | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+937dupG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067495 | ||||||
chr22:50067495
|
TCCCCTGT others(17): Show |
T | 3 | a0001c0001t0002g0117a0001c0001t0012g0108a0001c0001t0012g0116 | 3 | HG00733.hp2 HG02148.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.894+914_894+937del others(24): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067495 | ||||||
chr22:50067497
|
C | G | 1 | a0001c0001t0003g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.894+936G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067497 | ||||||
chr22:50067500
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+933A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067500 | ||||||
chr22:50067524
|
T | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(15): Show | 21 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.894+909A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067524 | ||||||
chr22:50067525
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+908C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067525 | ||||||
chr22:50067545
|
C | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+888G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067545 | ||||||
chr22:50067549
|
A | G | 7 | a0001c0001t0024g0146a0001c0005t0013g0064a0002c0002t0007g0165others(4): Show | 7 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+884T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067549 | ||||||
chr22:50067573
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.894+860C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067573 | ||||||
chr22:50067596
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+837C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067596 | ||||||
chr22:50067601
|
GCAGTGAC others(12): Show |
G | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 64 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.894+813_894+831del others(19): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067601 | ||||||
chr22:50067619
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+814T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067619 | ||||||
chr22:50067620
|
T | TCAGG | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+812_894+813ins others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067620 | ||||||
chr22:50067639
|
TCAGA | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+790_894+793del others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067639 | ||||||
chr22:50067672
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.894+761T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067672 | ||||||
chr22:50067689
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+744C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067689 | ||||||
chr22:50067697
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+736G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067697 | ||||||
chr22:50067703
|
CTCCATCA others(17): Show |
C | 1 | a0001c0001t0002g0147 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.894+706_894+729del others(24): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067703 | ||||||
chr22:50067704
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+729A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067704 | ||||||
chr22:50067712
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+721T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067712 | ||||||
chr22:50067720
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+713A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067720 | ||||||
chr22:50067726
|
CA | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+706delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067726 | ||||||
chr22:50067750
|
CA | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+682delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067750 | ||||||
chr22:50067752
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+681A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067752 | ||||||
chr22:50067772
|
TC | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+660delG | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067772 | ||||||
chr22:50067806
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+627T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067806 | ||||||
chr22:50067818
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0065 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.894+615A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067818 | ||||||
chr22:50067819
|
C | G | 1 | a0001c0001t0002g0155 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.894+614G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067819 | ||||||
chr22:50067956
|
A | C | 58 | a0001c0001t0001g0075a0001c0001t0001g0103a0001c0001t0001g0133others(55): Show | 64 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.894+477T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067956 | ||||||
chr22:50067963
|
C | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0120 | 2 | NA18944.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.894+470G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067963 | ||||||
chr22:50067971
|
C | A | 6 | a0001c0001t0001g0096a0002c0002t0007g0165a0002c0002t0007g0166others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.894+462G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50067971 | ||||||
chr22:50068011
|
C | T | 21 | a0001c0001t0003g0004a0001c0001t0003g0169a0001c0001t0003g0170others(18): Show | 23 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+422G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068011 | ||||||
chr22:50068234
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+199C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068234 | ||||||
chr22:50068239
|
C | T | 57 | a0001c0001t0001g0075a0001c0001t0001g0103a0001c0001t0001g0133others(54): Show | 63 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.894+194G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068239 | ||||||
chr22:50068305
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.894+128C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068305 | ||||||
chr22:50068381
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+52T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 10/11 | chr22 | 50068381 | ||||||
chr22:50068589
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.772-34G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068589 | ||||||
chr22:50068590
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-35C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068590 | ||||||
chr22:50068635
|
G | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-80C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068635 | ||||||
chr22:50068665
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-110A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068665 | ||||||
chr22:50068725
|
C | CT | 29 | a0001c0001t0001g0032a0001c0001t0001g0086a0001c0001t0001g0099others(26): Show | 32 | HG00099.hp1 HG01070.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.772-171dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | ||||||
chr22:50068725
|
C | CTT | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0067others(10): Show | 16 | HG00741.hp1 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.772-172_772-171dup others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | ||||||
chr22:50068725
|
CT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0002g0117others(5): Show | 9 | HG01255.hp2 HG02148.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.772-171delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | ||||||
chr22:50068725
|
CTTTT | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(44): Show | 51 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.772-174_772-171del others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068725 | ||||||
chr22:50068727
|
T | TTTC | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-173_772-172ins others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068727 | ||||||
chr22:50068730
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0025g0190others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-175A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068730 | ||||||
chr22:50068732
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-177A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068732 | ||||||
chr22:50068872
|
G | A | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.772-317C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068872 | ||||||
chr22:50068918
|
T | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-363A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068918 | ||||||
chr22:50068929
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-374C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068929 | ||||||
chr22:50068978
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-423G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50068978 | ||||||
chr22:50069098
|
A | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-543T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069098 | ||||||
chr22:50069310
|
G | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-755C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069310 | ||||||
chr22:50069357
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-802G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069357 | ||||||
chr22:50069372
|
A | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-817T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069372 | ||||||
chr22:50069410
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0032 | 3 | HG02451.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.772-855G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069410 | ||||||
chr22:50069487
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-932C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069487 | ||||||
chr22:50069512
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.772-957C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069512 | ||||||
chr22:50069514
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.772-959G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069514 | ||||||
chr22:50069515
|
G | C | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.772-960C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069515 | ||||||
chr22:50069607
|
C | T | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.771+920G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069607 | ||||||
chr22:50069710
|
C | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+817G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069710 | ||||||
chr22:50069763
|
C | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+764G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069763 | ||||||
chr22:50069776
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0011g0030a0001c0001t0011g0081others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+751C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069776 | ||||||
chr22:50069902
|
T | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+625A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069902 | ||||||
chr22:50069920
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+607C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069920 | ||||||
chr22:50069923
|
C | T | 1 | a0001c0001t0001g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.771+604G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069923 | ||||||
chr22:50069999
|
C | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+528G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50069999 | ||||||
chr22:50070074
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.771+453G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070074 | ||||||
chr22:50070139
|
T | A | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.771+388A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070139 | ||||||
chr22:50070157
|
G | A | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+370C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070157 | ||||||
chr22:50070243
|
A | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 53 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.771+284T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070243 | ||||||
chr22:50070270
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.771+257G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070270 | ||||||
chr22:50070273
|
A | C | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+254T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070273 | ||||||
chr22:50070291
|
C | T | 8 | a0001c0001t0002g0017a0001c0001t0002g0102a0001c0001t0002g0136others(5): Show | 9 | NA18945.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.771+236G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070291 | ||||||
chr22:50070292
|
G | A | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 53 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.771+235C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070292 | ||||||
chr22:50070321
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.771+206C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070321 | ||||||
chr22:50070352
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+175T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070352 | ||||||
chr22:50070367
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+160T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070367 | ||||||
chr22:50070405
|
G | T | 1 | a0001c0001t0003g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.771+122C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070405 | ||||||
chr22:50070409
|
C | T | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.771+118G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070409 | ||||||
chr22:50070466
|
A | G | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+61T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070466 | ||||||
chr22:50070468
|
G | T | 5 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+59C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 9/11 | chr22 | 50070468 | ||||||
chr22:50070755
|
C | T | 1 | a0001c0001t0013g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.715-172G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50070755 | ||||||
chr22:50070767
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 55 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.715-184C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50070767 | ||||||
chr22:50071014
|
G | A | 1 | a0004c0004t0022g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-431C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071014 | ||||||
chr22:50071115
|
C | CT | 18 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0048others(15): Show | 22 | HG00673.hp1 HG01243.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.715-533dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071115 | ||||||
chr22:50071246
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 189 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.715-663A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071246 | ||||||
chr22:50071323
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(10): Show | 16 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.715-740G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071323 | ||||||
chr22:50071334
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.715-751G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071334 | ||||||
chr22:50071461
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.715-878C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071461 | ||||||
chr22:50071488
|
C | T | 13 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(10): Show | 14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-905G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071488 | ||||||
chr22:50071489
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0025g0190 | 3 | HG02257.hp1 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.715-906C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071489 | ||||||
chr22:50071548
|
A | G | 14 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(11): Show | 15 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-965T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071548 | ||||||
chr22:50071582
|
T | A | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-999A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071582 | ||||||
chr22:50071586
|
C | T | 13 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(10): Show | 14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-1003G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071586 | ||||||
chr22:50071590
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 206 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.715-1007A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071590 | ||||||
chr22:50071703
|
T | A | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-1120A>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071703 | ||||||
chr22:50071829
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 139 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.715-1246A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071829 | ||||||
chr22:50071949
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.715-1366C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071949 | ||||||
chr22:50071949
|
G | C | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.715-1366C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071949 | ||||||
chr22:50071981
|
G | C | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-1398C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071981 | ||||||
chr22:50071982
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.715-1399G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50071982 | ||||||
chr22:50072003
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.715-1420C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072003 | ||||||
chr22:50072104
|
A | T | 13 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(10): Show | 14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-1521T>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072104 | ||||||
chr22:50072161
|
C | T | 1 | a0003c0003t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.715-1578G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072161 | ||||||
chr22:50072180
|
G | A | 1 | a0004c0004t0022g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-1597C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072180 | ||||||
chr22:50072267
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | HG02027.hp1 NA19060.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.715-1684T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072267 | ||||||
chr22:50072420
|
T | C | 14 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(11): Show | 15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.714+1796A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072420 | ||||||
chr22:50072496
|
G | A | 12 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(9): Show | 13 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.714+1720C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072496 | ||||||
chr22:50072534
|
C | G | 2 | a0001c0001t0001g0083a0001c0001t0013g0089 | 2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.714+1682G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072534 | ||||||
chr22:50072534
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(11): Show | 17 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+1682G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072534 | ||||||
chr22:50072601
|
T | G | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1615A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072601 | ||||||
chr22:50072799
|
T | C | 2 | a0001c0001t0004g0175a0001c0001t0004g0181 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.714+1417A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072799 | ||||||
chr22:50072835
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1381A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072835 | ||||||
chr22:50072837
|
C | G | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1379G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072837 | ||||||
chr22:50072842
|
G | T | 1 | a0001c0001t0002g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.714+1374C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072842 | ||||||
chr22:50072945
|
T | C | 13 | a0001c0001t0001g0120a0001c0001t0002g0114a0001c0001t0002g0117others(10): Show | 14 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+1271A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072945 | ||||||
chr22:50072973
|
A | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0026others(66): Show | 80 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.714+1243T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072973 | ||||||
chr22:50072997
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | NA19066.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.714+1219C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50072997 | ||||||
chr22:50073026
|
GGCAGTCC others(42): Show |
G | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.714+1141_714+1189d others(51): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073026 | ||||||
chr22:50073038
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+1178C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073038 | ||||||
chr22:50073046
|
C | CGCTCCCG others(42): Show |
14 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(11): Show | 15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.714+1169_714+1170i others(51): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073046 | ||||||
chr22:50073085
|
C | G | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.714+1131G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073085 | ||||||
chr22:50073086
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.714+1130G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073086 | ||||||
chr22:50073109
|
C | T | 6 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+1107G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073109 | ||||||
chr22:50073275
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(11): Show | 17 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+941T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073275 | ||||||
chr22:50073317
|
C | T | 6 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+899G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073317 | ||||||
chr22:50073378
|
C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 21 | HG00544.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.714+838G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073378 | ||||||
chr22:50073390
|
G | A | 1 | a0004c0004t0004g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.714+826C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073390 | ||||||
chr22:50073559
|
G | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0026others(67): Show | 81 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.714+657C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073559 | ||||||
chr22:50073683
|
G | A | 2 | a0001c0001t0010g0014a0001c0001t0016g0107 | 3 | HG02004.hp2 HG02273.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.714+533C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073683 | ||||||
chr22:50073687
|
T | G | 14 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(11): Show | 15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.714+529A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073687 | ||||||
chr22:50073906
|
A | G | 1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.714+310T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50073906 | ||||||
chr22:50074065
|
C | G | 1 | a0001c0001t0002g0142 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.714+151G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074065 | ||||||
chr22:50074085
|
T | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0026others(73): Show | 87 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+131A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074085 | ||||||
chr22:50074086
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.714+130C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074086 | ||||||
chr22:50074188
|
C | T | 36 | a0001c0001t0001g0120a0001c0001t0001g0161a0001c0001t0001g0185others(33): Show | 39 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.714+28G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 8/11 | chr22 | 50074188 | ||||||
chr22:50074341
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.598-9C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074341 | ||||||
chr22:50074504
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.598-172G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074504 | ||||||
chr22:50074796
|
TG | T | 44 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0001others(41): Show | 49 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-465delC | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074796 | ||||||
chr22:50074976
|
A | C | 28 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0001g0120others(25): Show | 32 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-644T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50074976 | ||||||
chr22:50075020
|
G | A | 1 | a0001c0001t0023g0098 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.598-688C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075020 | ||||||
chr22:50075101
|
AGGGCCGC others(25): Show |
A | 17 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(14): Show | 20 | HG00741.hp2 HG01071.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-801_598-770del others(32): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075101 | ||||||
chr22:50075101
|
AGGGCCGC others(57): Show |
A | 3 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0007t0001g0054 | 3 | NA18966.hp2 NA19060.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.598-833_598-770del others(64): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075101 | ||||||
chr22:50075170
|
C | CGCAACCA others(89): Show |
1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598-839_598-838ins others(96): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075170 | ||||||
chr22:50075202
|
C | A | 25 | a0001c0001t0001g0161a0001c0001t0001g0185a0001c0001t0001g0188others(22): Show | 28 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.598-870G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075202 | ||||||
chr22:50075272
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.598-940C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075272 | ||||||
chr22:50075285
|
T | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0026others(76): Show | 90 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.598-953A>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075285 | ||||||
chr22:50075355
|
G | A | 14 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(11): Show | 15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.598-1023C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075355 | ||||||
chr22:50075442
|
C | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(40): Show | 49 | HG00544.hp2 HG00741.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.598-1110G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075442 | ||||||
chr22:50075691
|
C | CAG | 187 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(184): Show | 209 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.597+1148_597+1149d others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075691 | ||||||
chr22:50075718
|
G | GA | 6 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+1122dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075718 | ||||||
chr22:50075969
|
C | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 21 | HG00544.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.597+872G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50075969 | ||||||
chr22:50076032
|
T | C | 15 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+809A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076032 | ||||||
chr22:50076076
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.597+765G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076076 | ||||||
chr22:50076182
|
C | CAT | 15 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+658_597+659ins others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076182 | ||||||
chr22:50076226
|
A | G | 3 | a0001c0001t0009g0011a0001c0001t0009g0078a0001c0001t0009g0088 | 4 | HG01255.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+615T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076226 | ||||||
chr22:50076283
|
G | A | 6 | a0002c0002t0007g0165a0002c0002t0007g0166a0002c0002t0007g0167others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+558C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076283 | ||||||
chr22:50076393
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.597+448T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076393 | ||||||
chr22:50076415
|
C | T | 1 | a0001c0007t0001g0054 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.597+426G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076415 | ||||||
chr22:50076470
|
A | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0026others(68): Show | 79 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.597+371T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076470 | ||||||
chr22:50076554
|
C | CA | 6 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0048others(3): Show | 6 | HG00099.hp1 HG02293.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+286dupT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076554 | ||||||
chr22:50076554
|
CA | C | 6 | a0001c0001t0001g0042a0001c0001t0002g0114a0001c0001t0003g0182others(3): Show | 7 | HG00673.hp2 HG01192.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+286delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076554 | ||||||
chr22:50076577
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0065 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.597+264C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076577 | ||||||
chr22:50076807
|
T | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(11): Show | 17 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.597+34A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 7/11 | chr22 | 50076807 | ||||||
chr22:50077030
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 190 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.526-118C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077030 | ||||||
chr22:50077208
|
G | A | 1 | a0001c0001t0025g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.525+193C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077208 | ||||||
chr22:50077248
|
C | T | 21 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0003g0004others(18): Show | 23 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.525+153G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077248 | ||||||
chr22:50077337
|
C | T | 15 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.525+64G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077337 | ||||||
chr22:50077379
|
C | T | 15 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.525+22G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 6/11 | chr22 | 50077379 | ||||||
chr22:50077512
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.424-10C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077512 | ||||||
chr22:50077611
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0011g0081a0001c0001t0018g0082 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.424-109G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077611 | ||||||
chr22:50077766
|
T | C | 43 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0001others(40): Show | 48 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.424-264A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077766 | ||||||
chr22:50077792
|
G | A | 1 | a0006c0008t0007g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.424-290C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077792 | ||||||
chr22:50077865
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.424-363T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077865 | ||||||
chr22:50077939
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 5 | HG02258.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-437C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077939 | ||||||
chr22:50077991
|
A | AT | 33 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0080others(30): Show | 37 | HG00741.hp1 HG01106.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.424-490dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | ||||||
chr22:50077991
|
A | ATT | 6 | a0001c0005t0013g0064a0002c0002t0007g0165a0002c0002t0007g0166others(3): Show | 6 | HG00673.hp1 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-491_424-490dup others(2): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | ||||||
chr22:50077991
|
A | ATTT | 14 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0114others(11): Show | 15 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-492_424-490dup others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | ||||||
chr22:50077991
|
AT | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02055.hp2 HG02056.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-490delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50077991 | ||||||
chr22:50078178
|
G | C | 1 | a0001c0001t0012g0108 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.424-676C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078178 | ||||||
chr22:50078226
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0065 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.424-724C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078226 | ||||||
chr22:50078608
|
G | A | 2 | a0001c0001t0002g0156a0001c0001t0025g0190 | 2 | HG02257.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.424-1106C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078608 | ||||||
chr22:50078631
|
C | G | 1 | a0001c0001t0002g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.424-1129G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078631 | ||||||
chr22:50078736
|
CA | C | 5 | a0001c0001t0002g0125a0001c0001t0002g0130a0001c0001t0021g0189others(2): Show | 5 | HG00438.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+1181delT | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078736 | ||||||
chr22:50078900
|
G | A | 15 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.423+1018C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50078900 | ||||||
chr22:50079009
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0074 | 3 | HG02055.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.423+909G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079009 | ||||||
chr22:50079252
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0065 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.423+666G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079252 | ||||||
chr22:50079313
|
A | G | 15 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.423+605T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079313 | ||||||
chr22:50079348
|
C | T | 21 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0003g0004others(18): Show | 23 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+570G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079348 | ||||||
chr22:50079500
|
C | CT | 20 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0026others(17): Show | 23 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+417dupA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | ||||||
chr22:50079500
|
C | CTTT | 9 | a0001c0001t0001g0120a0001c0001t0002g0114a0001c0001t0002g0117others(6): Show | 10 | HG00673.hp2 HG01358.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+415_423+417dup others(3): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | ||||||
chr22:50079500
|
C | CTTTT | 6 | a0001c0001t0002g0106a0001c0001t0002g0113a0001c0001t0006g0112others(3): Show | 6 | HG00621.hp1 HG00733.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+414_423+417dup others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | ||||||
chr22:50079500
|
CT | C | 24 | a0001c0001t0001g0045a0001c0001t0001g0185a0001c0001t0001g0188others(21): Show | 26 | HG00741.hp1 HG01070.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.423+417delA | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | ||||||
chr22:50079500
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.423+406_423+417del others(12): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079500 | ||||||
chr22:50079767
|
T | C | 2 | a0001c0001t0021g0189a0001c0001t0025g0190 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.423+151A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079767 | ||||||
chr22:50079797
|
A | C | 2 | a0004c0004t0004g0164a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.423+121T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079797 | ||||||
chr22:50079810
|
T | C | 17 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(14): Show | 18 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.423+108A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079810 | ||||||
chr22:50079896
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.423+22G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 5/11 | chr22 | 50079896 | ||||||
chr22:50080222
|
G | A | 2 | a0001c0001t0021g0189a0001c0001t0025g0190 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.321+122C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 4/11 | chr22 | 50080222 | ||||||
chr22:50080266
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.321+78T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 4/11 | chr22 | 50080266 | ||||||
chr22:50080294
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 207 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.321+50T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 4/11 | chr22 | 50080294 | ||||||
chr22:50080749
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268-352T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50080749 | ||||||
chr22:50080903
|
G | C | 2 | a0001c0001t0020g0021a0004c0004t0004g0164 | 2 | HG00438.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.268-506C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50080903 | ||||||
chr22:50080982
|
G | A | 1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-585C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50080982 | ||||||
chr22:50081007
|
A | AAAAAAGA others(23): Show |
1 | a0001c0001t0002g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.268-640_268-611dup others(30): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081007 | ||||||
chr22:50081009
|
A | AAAAAGAA others(10): Show |
1 | a0001c0001t0001g0067 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAG | 7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 8 | HG01243.hp2 HG01256.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.268-616_268-613dup others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(1): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0090a0001c0001t0001g0093others(5): Show | 9 | HG00544.hp1 HG01243.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-620_268-613dup others(8): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(5): Show |
10 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0047others(7): Show | 11 | HG01358.hp1 HG01361.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.268-624_268-613dup others(12): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(9): Show |
15 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 18 | HG01256.hp1 HG01258.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.268-628_268-613dup others(16): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(13): Show |
19 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0031others(16): Show | 22 | HG00733.hp1 HG00733.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.268-632_268-613dup others(20): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(30): Show |
1 | a0004c0004t0022g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(37): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(17): Show |
22 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0023others(19): Show | 24 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.268-636_268-613dup others(24): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(21): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0076others(13): Show | 17 | HG00741.hp1 HG01070.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-640_268-613dup others(28): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(25): Show |
7 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0188others(4): Show | 8 | HG01255.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-644_268-613dup others(32): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(31): Show |
2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(38): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(29): Show |
2 | a0001c0001t0001g0032a0001c0001t0012g0108 | 2 | HG02148.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.268-648_268-613dup others(36): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAAGAAA others(33): Show |
3 | a0001c0001t0001g0036a0001c0001t0016g0107a0001c0001t0021g0189 | 3 | NA18952.hp1 NA19043.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.268-652_268-613dup others(40): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0040 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(19): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAGAAAG others(16): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0052 | 2 | HG03942.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(23): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAGAAAG others(24): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0128a0001c0001t0008g0049 | 3 | HG03239.hp1 NA19062.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(31): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAGAAAG others(28): Show |
1 | a0003c0003t0001g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(35): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAAGAGAA others(18): Show |
1 | a0001c0001t0001g0034 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(25): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAGAAAGA others(11): Show |
2 | a0001c0001t0001g0039a0001c0001t0008g0029 | 2 | HG01175.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.268-613_268-612ins others(18): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAGAAAGA others(15): Show |
1 | a0001c0001t0006g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAGAAAGA others(19): Show |
1 | a0001c0001t0001g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AAGAAGAA others(10): Show |
1 | a0001c0001t0001g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AGAAAGAA others(14): Show |
1 | a0001c0001t0020g0021 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(21): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AGAAAGAA others(22): Show |
1 | a0001c0001t0001g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268-613_268-612ins others(29): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
A | AGAAAGAA others(34): Show |
1 | a0001c0001t0001g0035 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.268-613_268-612ins others(41): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081009
|
AAAAG | A | 2 | a0001c0001t0005g0002a0001c0001t0005g0028 | 4 | HG02055.hp1 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-616_268-613del others(4): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081009 | ||||||
chr22:50081013
|
G | GAAAGAAA others(15): Show |
1 | a0001c0001t0001g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.268-638_268-617dup others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081013 | ||||||
chr22:50081013
|
G | GAAAGAAA others(19): Show |
6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0016others(3): Show | 7 | HG01106.hp1 HG02280.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-642_268-617dup others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081013 | ||||||
chr22:50081014
|
A | AAAGAAAG others(20): Show |
1 | a0001c0001t0002g0127 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.268-644_268-618dup others(27): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081014 | ||||||
chr22:50081017
|
G | GAAAGAAA others(15): Show |
25 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0102others(22): Show | 29 | HG00099.hp2 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.268-642_268-621dup others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081017 | ||||||
chr22:50081017
|
G | GAAAGAAA others(19): Show |
4 | a0001c0001t0002g0124a0001c0001t0002g0136a0001c0001t0002g0137others(1): Show | 4 | HG02015.hp1 HG02148.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-646_268-621dup others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081017 | ||||||
chr22:50081021
|
G | GAAAGAAA others(11): Show |
2 | a0001c0001t0002g0123a0001c0001t0002g0162 | 2 | HG02135.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.268-642_268-625dup others(18): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081021 | ||||||
chr22:50081025
|
G | GAAAGAAA others(7): Show |
1 | a0005c0006t0002g0157 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.268-642_268-629dup others(14): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081025 | ||||||
chr22:50081029
|
G | GAAAGAAA others(16): Show |
1 | a0001c0001t0002g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.268-633_268-632ins others(23): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081029 | ||||||
chr22:50081033
|
G | GAAAGAAA others(43): Show |
1 | a0001c0005t0013g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-637_268-636ins others(50): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081033 | ||||||
chr22:50081037
|
G | GAAAGAAA others(38): Show |
1 | a0001c0001t0004g0187 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.268-641_268-640ins others(45): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081037 | ||||||
chr22:50081049
|
G | GAAAGAAA others(7): Show |
1 | a0001c0001t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.268-653_268-652ins others(14): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | ||||||
chr22:50081049
|
G | GAAAGAAA others(11): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.268-653_268-652ins others(18): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | ||||||
chr22:50081049
|
G | GAAAGAAA others(15): Show |
1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.268-653_268-652ins others(22): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | ||||||
chr22:50081049
|
G | GAAAGAAA others(19): Show |
1 | a0001c0001t0001g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.268-653_268-652ins others(26): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | ||||||
chr22:50081049
|
G | GAAAGAAA others(23): Show |
1 | a0001c0001t0001g0003 | 3 | HG00741.hp2 HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.268-653_268-652ins others(30): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | ||||||
chr22:50081049
|
G | GAAAGAAA others(27): Show |
2 | a0001c0001t0001g0069a0003c0003t0001g0068 | 2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.268-653_268-652ins others(34): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081049 | ||||||
chr22:50081151
|
C | T | 17 | a0001c0001t0001g0120a0001c0001t0002g0106a0001c0001t0002g0113others(14): Show | 18 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.268-754G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081151 | ||||||
chr22:50081203
|
C | T | 1 | a0001c0009t0014g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.268-806G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081203 | ||||||
chr22:50081215
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(60): Show | 74 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.268-818A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081215 | ||||||
chr22:50081338
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-941C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081338 | ||||||
chr22:50081439
|
ACAGCCTT others(8): Show |
A | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.268-1057_268-1043d others(17): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081439 | ||||||
chr22:50081444
|
C | T | 3 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126 | 3 | HG02015.hp1 HG02074.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.268-1047G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081444 | ||||||
chr22:50081549
|
G | A | 3 | a0001c0001t0002g0106a0001c0001t0010g0014a0001c0001t0016g0107 | 4 | HG02004.hp2 HG02273.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-1152C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081549 | ||||||
chr22:50081553
|
C | A | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.268-1156G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081553 | ||||||
chr22:50081610
|
C | T | 3 | a0001c0001t0002g0106a0001c0001t0010g0014a0001c0001t0016g0107 | 4 | HG02004.hp2 HG02273.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-1213G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081610 | ||||||
chr22:50081623
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.268-1226C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081623 | ||||||
chr22:50081703
|
G | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0067a0001c0001t0001g0069others(7): Show | 12 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-1306C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081703 | ||||||
chr22:50081762
|
G | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0002g0113others(14): Show | 18 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.267+1322C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081762 | ||||||
chr22:50081955
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG00733.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.267+1129C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50081955 | ||||||
chr22:50082044
|
C | T | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+1040G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082044 | ||||||
chr22:50082050
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.267+1034G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082050 | ||||||
chr22:50082124
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.267+960G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082124 | ||||||
chr22:50082139
|
G | C | 2 | a0001c0001t0001g0161a0001c0001t0025g0190 | 2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.267+945C>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082139 | ||||||
chr22:50082157
|
C | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(5): Show | 8 | HG00438.hp2 HG02015.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+927G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082157 | ||||||
chr22:50082163
|
G | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 21 | HG00544.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.267+921C>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082163 | ||||||
chr22:50082167
|
GTGGGGTC others(24): Show |
G | 3 | a0001c0001t0001g0104a0001c0009t0014g0105a0004c0004t0022g0163 | 3 | HG01496.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.267+886_267+916del others(31): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082167 | ||||||
chr22:50082174
|
CCGCGGCT others(55): Show |
C | 15 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(12): Show | 16 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.267+848_267+909del others(62): Show |
MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082174 | ||||||
chr22:50082205
|
C | G | 1 | a0001c0001t0011g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.267+879G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082205 | ||||||
chr22:50082247
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.267+837C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082247 | ||||||
chr22:50082290
|
A | C | 1 | a0004c0004t0022g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.267+794T>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082290 | ||||||
chr22:50082409
|
C | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0031others(85): Show | 101 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.267+675G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082409 | ||||||
chr22:50082450
|
A | G | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+634T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082450 | ||||||
chr22:50082467
|
G | A | 1 | a0004c0004t0004g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.267+617C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082467 | ||||||
chr22:50082701
|
A | G | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+383T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082701 | ||||||
chr22:50082728
|
A | G | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+356T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082728 | ||||||
chr22:50082910
|
C | A | 1 | a0001c0001t0005g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.267+174G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 3/11 | chr22 | 50082910 | ||||||
chr22:50083305
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.178-132T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083305 | ||||||
chr22:50083346
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.178-173G>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083346 | ||||||
chr22:50083346
|
C | T | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-173G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083346 | ||||||
chr22:50083352
|
C | A | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-179G>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083352 | ||||||
chr22:50083707
|
T | C | 16 | a0001c0001t0001g0120a0001c0001t0002g0113a0001c0001t0002g0114others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-534A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083707 | ||||||
chr22:50083724
|
G | A | 44 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0133others(41): Show | 49 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.178-551C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083724 | ||||||
chr22:50083886
|
T | C | 102 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0031others(99): Show | 115 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.178-713A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50083886 | ||||||
chr22:50084032
|
G | A | 4 | a0001c0001t0001g0161a0001c0001t0002g0162a0001c0001t0021g0189others(1): Show | 4 | HG02135.hp2 HG02257.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+694C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084032 | ||||||
chr22:50084037
|
C | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 48 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.177+689G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084037 | ||||||
chr22:50084095
|
C | T | 2 | a0004c0004t0004g0164a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+631G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084095 | ||||||
chr22:50084248
|
G | A | 2 | a0004c0004t0004g0164a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+478C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084248 | ||||||
chr22:50084273
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 5 | HG02258.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+453G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084273 | ||||||
chr22:50084501
|
A | G | 2 | a0004c0004t0004g0164a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+225T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084501 | ||||||
chr22:50084649
|
C | T | 1 | a0001c0001t0008g0029 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+77G>A | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 2/11 | chr22 | 50084649 | ||||||
chr22:50084978
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0005g0002a0001c0001t0005g0005others(2): Show | 8 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-59-17T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50084978 | ||||||
chr22:50084988
|
G | A | 2 | a0004c0004t0004g0164a0004c0004t0022g0163 | 2 | HG03471.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-59-27C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50084988 | ||||||
chr22:50085004
|
T | C | 25 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0003g0004others(22): Show | 27 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-59-43A>G | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50085004 | ||||||
chr22:50085241
|
G | A | 2 | a0001c0001t0021g0189a0001c0001t0025g0190 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-60+114C>T | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50085241 | ||||||
chr22:50085316
|
A | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(5): Show | 8 | HG00438.hp2 HG02015.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.-60+39T>C | MLC1 | ENSG00000100427.16 | transcript | ENST00000311597.10 | protein_coding | 1/11 | chr22 | 50085316 |