geneid | 79258 |
---|---|
ensemblid | ENSG00000142606.16 |
hgncid | 14668 |
symbol | MMEL1 |
name | membrane metalloendopeptidase like 1 |
refseq_nuc | NM_033467.4 |
refseq_prot | NP_258428.2 |
ensembl_nuc | ENST00000378412.8 |
ensembl_prot | ENSP00000367668.3 |
mane_status | MANE Select |
chr | chr1 |
start | 2590639 |
end | 2633016 |
strand | - |
ver | v1.2 |
region | chr1:2590639-2633016 |
region5000 | chr1:2585639-2638016 |
regionname0 | MMEL1_chr1_2590639_2633016 |
regionname5000 | MMEL1_chr1_2585639_2638016 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 779 | 166 | 30 | 30 | 72 | 11 | 22 | 52 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002 | 0/0 | 779 | 161 | 50 | 30 | 63 | 3 | 15 | 50 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0003 | 0/0 | 779 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0004 | 0/0 | 779 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0005 | 0/0 | 779 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0006 | 0/0 | 779 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0007 | 0/0 | 779 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0008 | 0/0 | 779 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0009 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0010 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0011 | 0/0 | 779 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0012 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0013 | 0/0 | 779 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2340 | 160 | 29 | 29 | 68 | 11 | 22 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0002 | 0/0 | 2340 | 137 | 33 | 29 | 58 | 2 | 15 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0003 | 0/0 | 2340 | 11 | 7 | 1 | 2 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0004 | 0/0 | 2340 | 5 | 5 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0005 | 0/0 | 2340 | 3 | 1 | 1 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0006 | 0/0 | 2340 | 3 | 0 | 2 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0007 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0008 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0009 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0010 | 0/0 | 2340 | 2 | 1 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0011 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0012 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0013 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0014 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0015 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0016 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0017 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0018 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0019 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0020 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0021 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0022 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0023 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0024 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0025 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
c0026 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 540 | 211 | 83 | 37 | 64 | 8 | 18 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
t0002 | 0/0 | 540 | 73 | 1 | 14 | 44 | 6 | 8 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
t0003 | 0/0 | 540 | 54 | 1 | 13 | 27 | 1 | 12 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
t0004 | 0/0 | 540 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
t0005 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
t0006 | 0/0 | 540 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
t0007 | 0/0 | 540 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0002 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0027 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2340 | 160 | 29 | 29 | 68 | 11 | 22 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0005 | 0/0 | 2340 | 3 | 1 | 1 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0014 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0021 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0022 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0002 | 0/0 | 2340 | 137 | 33 | 29 | 58 | 2 | 15 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0003 | 0/0 | 2340 | 11 | 7 | 1 | 2 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0004 | 0/0 | 2340 | 5 | 5 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0008 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0012 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0016 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0017 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0018 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0023 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0025 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0003c0006 | 0/0 | 2340 | 3 | 0 | 2 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0004c0007 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0005c0010 | 0/0 | 2340 | 2 | 1 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0006c0009 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0007c0026 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0008c0011 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0009c0024 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0010c0015 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0011c0020 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0012c0013 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0013c0019 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2879 | 88 | 27 | 16 | 24 | 6 | 14 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0001t0002 | 0/0 | 2879 | 70 | 1 | 13 | 43 | 5 | 8 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0001t0005 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0001t0007 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0005t0001 | 0/0 | 2879 | 3 | 1 | 1 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0014t0002 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0021t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0001c0022t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0002t0001 | 0/0 | 2879 | 85 | 33 | 17 | 31 | 1 | 3 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0002t0003 | 0/0 | 2879 | 52 | 0 | 12 | 27 | 1 | 12 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0003t0001 | 0/0 | 2879 | 10 | 7 | 1 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0003t0006 | 0/0 | 2879 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0004t0001 | 0/0 | 2879 | 5 | 5 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0008t0001 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0012t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0016t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0017t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0018t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0023t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0002c0025t0003 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0003c0006t0001 | 0/0 | 2879 | 3 | 0 | 2 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0004c0007t0001 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0005c0010t0001 | 0/0 | 2879 | 2 | 1 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0006c0009t0004 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0007c0026t0002 | 0/0 | 2879 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0008c0011t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0009c0024t0002 | 0/0 | 2879 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0010c0015t0003 | 0/0 | 2879 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0011c0020t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0012c0013t0001 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
a0013c0019t0001 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | copy fasta | chr1 | 2585639 | 2638016 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0027 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0014t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0021t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0001c0022t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0002 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0003t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0008t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0012t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0016t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0017t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0018t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0023t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0002c0025t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0003c0006t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0003c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0004c0007t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0005c0010t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0005c0010t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0006c0009t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0006c0009t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0007c0026t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0008c0011t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0009c0024t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0010c0015t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0011c0020t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0012c0013t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
a0013c0019t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0056 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00099 | hp2 | a0007 | c0026 | t0002 | g0244 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00140 | hp2 | a0002 | c0003 | t0006 | g0131 | EUR | GBR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0183 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00323 | hp1 | a0005 | c0010 | t0001 | g0236 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00408 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00438 | hp1 | a0002 | c0018 | t0001 | g0114 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00544 | hp1 | a0002 | c0002 | t0003 | g0112 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00597 | hp1 | a0002 | c0002 | t0003 | g0122 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00642 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00733 | hp2 | a0002 | c0002 | t0003 | g0015 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00735 | hp2 | a0003 | c0006 | t0001 | g0024 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00738 | hp2 | a0002 | c0002 | t0003 | g0037 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00741 | hp1 | a0009 | c0024 | t0002 | g0136 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG00741 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01069 | hp1 | a0003 | c0006 | t0001 | g0024 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0033 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01255 | hp1 | a0001 | c0005 | t0001 | g0062 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01255 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01346 | hp1 | a0010 | c0015 | t0003 | g0039 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01346 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01361 | hp2 | a0002 | c0002 | t0003 | g0088 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01433 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | IBS | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01884 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01891 | hp1 | a0002 | c0016 | t0001 | g0042 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01978 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02040 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02055 | hp1 | a0005 | c0010 | t0001 | g0241 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02055 | hp2 | a0002 | c0012 | t0001 | g0126 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02074 | hp1 | a0001 | c0014 | t0002 | g0120 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02080 | hp2 | a0012 | c0013 | t0001 | g0097 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02083 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PEL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02280 | hp2 | a0002 | c0008 | t0001 | g0050 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | KHV | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02572 | hp2 | a0011 | c0020 | t0001 | g0266 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02615 | hp2 | a0002 | c0004 | t0001 | g0270 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02630 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02630 | hp2 | a0002 | c0004 | t0001 | g0269 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02647 | hp1 | a0008 | c0011 | t0001 | g0128 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0032 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02698 | hp1 | a0002 | c0002 | t0003 | g0036 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02717 | hp1 | a0002 | c0004 | t0001 | g0275 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02723 | hp2 | a0002 | c0004 | t0001 | g0268 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0092 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02965 | hp2 | a0006 | c0009 | t0004 | g0277 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02976 | hp1 | a0013 | c0019 | t0001 | g0271 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03130 | hp2 | a0002 | c0003 | t0001 | g0278 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03225 | hp2 | a0004 | c0007 | t0001 | g0029 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03453 | hp2 | a0004 | c0007 | t0001 | g0029 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0034 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03579 | hp1 | a0002 | c0003 | t0001 | g0280 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03669 | hp2 | a0002 | c0002 | t0003 | g0099 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0015 | SAS | PJL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0116 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03942 | hp1 | a0003 | c0006 | t0001 | g0157 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04184 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0084 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0106 | SAS | STU | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18747 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18906 | hp2 | a0002 | c0004 | t0001 | g0267 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18940 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18956 | hp2 | a0001 | c0021 | t0001 | g0159 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18963 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18969 | hp2 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18977 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18979 | hp2 | a0002 | c0002 | t0003 | g0080 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18984 | hp1 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18999 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19003 | hp1 | a0002 | c0002 | t0003 | g0089 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19067 | hp2 | a0001 | c0005 | t0001 | g0082 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19079 | hp2 | a0002 | c0023 | t0001 | g0258 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19081 | hp2 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19087 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19089 | hp2 | a0002 | c0017 | t0001 | g0129 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | YRI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | ASW | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | ASW | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0038 | EUR | TSI | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20905 | hp1 | a0002 | c0002 | t0003 | g0105 | SAS | GIH | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0028 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02109 | hp1 | a0002 | c0025 | t0003 | g0225 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02559 | hp1 | a0006 | c0009 | t0004 | g0276 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG06807 | hp1 | a0002 | c0008 | t0001 | g0049 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18955 | hp1 | a0001 | c0022 | t0001 | g0177 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | USA | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | LWK | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0027 | REF | REF | MMEL1_chr1_2585639_2638016 | MMEL1 | chr1 | 2585639 | 2638016 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2591973
|
C | T | 1 | a0009 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2122G>A | p.Asp708Asn | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/24 | 2310/2879 | 2122/2340 | 708/779 | chr1 | 2591973 | ||
chr1:2591992
|
G | T | 1 | a0003 | 3 | HG00735.hp2 HG01069.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.2103C>A | p.Asp701Glu | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/24 | 2291/2879 | 2103/2340 | 701/779 | chr1 | 2591992 | ||
chr1:2592689
|
A | G | 1 | a0005 | 2 | HG00323.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.2033T>C | p.Ile678Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/24 | 2221/2879 | 2033/2340 | 678/779 | chr1 | 2592689 | ||
chr1:2595307
|
A | G | 8 | a0002a0004a0006others(5): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
missense_variant | MODERATE | c.1553T>C | p.Met518Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/24 | 1741/2879 | 1553/2340 | 518/779 | chr1 | 2595307 | ||
chr1:2603958
|
C | G | 1 | a0010 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.967G>C | p.Glu323Gln | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/24 | 1155/2879 | 967/2340 | 323/779 | chr1 | 2603958 | ||
chr1:2604193
|
T | C | 1 | a0006 | 2 | HG02559.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.905A>G | p.Gln302Arg | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1093/2879 | 905/2340 | 302/779 | chr1 | 2604193 | ||
chr1:2604278
|
G | A | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.820C>T | p.Arg274Trp | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1008/2879 | 820/2340 | 274/779 | chr1 | 2604278 | ||
chr1:2606261
|
C | T | 2 | a0004a0013 | 3 | HG02976.hp1 HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.737G>A | p.Arg246Gln | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/24 | 925/2879 | 737/2340 | 246/779 | chr1 | 2606261 | ||
chr1:2606280
|
C | T | 1 | a0012 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.718G>A | p.Asp240Asn | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/24 | 906/2879 | 718/2340 | 240/779 | chr1 | 2606280 | ||
chr1:2609389
|
C | G | 1 | a0008 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.485G>C | p.Arg162Pro | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/24 | 673/2879 | 485/2340 | 162/779 | chr1 | 2609389 | ||
chr1:2609829
|
C | T | 1 | a0013 | 1 | HG02976.hp1 | missense_variant&splice_region_variant | MODERATE | c.295G>A | p.Ala99Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/24 | 483/2879 | 295/2340 | 99/779 | chr1 | 2609829 | ||
chr1:2612197
|
C | A | 1 | a0007 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.162G>T | p.Gln54His | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/24 | 350/2879 | 162/2340 | 54/779 | chr1 | 2612197 | ||
chr1:2629468
|
C | G | 1 | a0004 | 2 | HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.17G>C | p.Gly6Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 205/2879 | 17/2340 | 6/779 | chr1 | 2629468 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2593833
|
C | T | 1 | a0002c0008 | 2 | HG02280.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.1848G>A | p.Thr616Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/24 | 2036/2879 | 1848/2340 | 616/779 | chr1 | 2593833 | ||
chr1:2593842
|
G | A | 1 | a0002c0017 | 1 | NA19089.hp2 | synonymous_variant | LOW | c.1839C>T | p.His613His | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/24 | 2027/2879 | 1839/2340 | 613/779 | chr1 | 2593842 | ||
chr1:2596018
|
C | T | 1 | a0001c0022 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.1491G>A | p.Ala497Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/24 | 1679/2879 | 1491/2340 | 497/779 | chr1 | 2596018 | ||
chr1:2596033
|
C | T | 1 | a0002c0016 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1476G>A | p.Glu492Glu | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/24 | 1664/2879 | 1476/2340 | 492/779 | chr1 | 2596033 | ||
chr1:2604174
|
C | A | 14 | a0001c0005a0001c0021a0002c0002others(11): Show | 157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
synonymous_variant | LOW | c.924G>T | p.Val308Val | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1112/2879 | 924/2340 | 308/779 | chr1 | 2604174 | ||
chr1:2604240
|
C | T | 1 | a0013c0019 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.858G>A | p.Thr286Thr | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/24 | 1046/2879 | 858/2340 | 286/779 | chr1 | 2604240 | ||
chr1:2606362
|
G | A | 6 | a0002c0004a0002c0012a0004c0007others(3): Show | 12 | HG02055.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
synonymous_variant | LOW | c.636C>T | p.Leu212Leu | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/24 | 824/2879 | 636/2340 | 212/779 | chr1 | 2606362 | ||
chr1:2607005
|
C | T | 5 | a0002c0004a0002c0012a0004c0007others(2): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
synonymous_variant | LOW | c.600G>A | p.Pro200Pro | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/24 | 788/2879 | 600/2340 | 200/779 | chr1 | 2607005 | ||
chr1:2609830
|
A | G | 16 | a0001c0005a0001c0014a0001c0021others(13): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
splice_region_variant&synonymous_variant | LOW | c.294T>C | p.Ala98Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/24 | 482/2879 | 294/2340 | 98/779 | chr1 | 2609830 | ||
chr1:2629443
|
G | A | 9 | a0001c0001a0001c0021a0001c0022others(6): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
synonymous_variant | LOW | c.42C>T | p.Ala14Ala | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 230/2879 | 42/2340 | 14/779 | chr1 | 2629443 | ||
chr1:2629464
|
T | G | 15 | a0001c0001a0001c0021a0001c0022others(12): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
synonymous_variant | LOW | c.21A>C | p.Pro7Pro | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 209/2879 | 21/2340 | 7/779 | chr1 | 2629464 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2590765
|
G | T | 3 | a0002c0002t0003a0002c0025t0003a0010c0015t0003 | 54 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 225 | chr1 | 2590765 | |||||
chr1:2590917
|
G | A | 1 | a0002c0003t0006 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 73 | chr1 | 2590917 | |||||
chr1:2590931
|
C | T | 1 | a0001c0001t0007 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 59 | chr1 | 2590931 | |||||
chr1:2590953
|
G | A | 5 | a0001c0001t0002a0001c0001t0007a0001c0014t0002others(2): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 24/24 | 37 | chr1 | 2590953 | |||||
chr1:2629500
|
C | T | 1 | a0006c0009t0004 | 2 | HG02559.hp1 HG02965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-16G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/24 | 16 | chr1 | 2629500 | |||||
chr1:2632905
|
C | T | 1 | a0001c0001t0005 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/24 | 3421 | chr1 | 2632905 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2591413
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2240+144G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591413 | ||||||
chr1:2591461
|
T | C | 1 | a0012c0013t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2240+96A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591461 | ||||||
chr1:2591486
|
T | C | 7 | a0002c0002t0001g0007a0002c0002t0001g0047a0002c0002t0001g0057others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2240+71A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591486 | ||||||
chr1:2591495
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2240+62G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 23/23 | chr1 | 2591495 | ||||||
chr1:2591773
|
G | C | 119 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(116): Show | 155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2164-140C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/23 | chr1 | 2591773 | ||||||
chr1:2591905
|
T | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2163+27A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/23 | chr1 | 2591905 | ||||||
chr1:2591922
|
C | T | 3 | a0002c0002t0001g0102a0002c0002t0001g0103a0002c0012t0001g0126 | 3 | HG02055.hp2 HG02056.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2163+10G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 22/23 | chr1 | 2591922 | ||||||
chr1:2592031
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.2068-4G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592031 | ||||||
chr1:2592221
|
CG | C | 186 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0135others(183): Show | 230 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2068-195delC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592221 | ||||||
chr1:2592224
|
G | T | 1 | a0001c0001t0002g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2068-197C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592224 | ||||||
chr1:2592257
|
C | G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2068-230G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592257 | ||||||
chr1:2592267
|
C | T | 119 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(116): Show | 155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2068-240G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592267 | ||||||
chr1:2592282
|
C | T | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068-255G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592282 | ||||||
chr1:2592283
|
GCCCCCTC others(17): Show |
G | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068-280_2068-257d others(26): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592283 | ||||||
chr1:2592284
|
C | T | 121 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(118): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2068-257G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592284 | ||||||
chr1:2592305
|
T | C | 9 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(6): Show | 13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2068-278A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592305 | ||||||
chr1:2592307
|
C | CCCCCCTC others(41): Show |
5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068-281_2068-280i others(50): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592307 | ||||||
chr1:2592323
|
C | T | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068-296G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592323 | ||||||
chr1:2592330
|
GC | G | 113 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(110): Show | 149 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.2068-304delG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592330 | ||||||
chr1:2592347
|
A | G | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+308T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592347 | ||||||
chr1:2592353
|
ACGCCCCC others(200): Show |
A | 1 | a0002c0002t0001g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2067+95_2067+301de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592353 | ||||||
chr1:2592355
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2067+300C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592355 | ||||||
chr1:2592356
|
CCCCCTCC others(199): Show |
C | 2 | a0002c0002t0001g0060a0002c0002t0003g0085 | 2 | HG02083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2067+93_2067+298de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592356 | ||||||
chr1:2592368
|
C | A | 116 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(113): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2067+287G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592368 | ||||||
chr1:2592369
|
T | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+286A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592369 | ||||||
chr1:2592371
|
T | C | 118 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(115): Show | 155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2067+284A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592371 | ||||||
chr1:2592372
|
G | A | 116 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(113): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2067+283C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592372 | ||||||
chr1:2592375
|
GGCACCCC others(37): Show |
G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+236_2067+279d others(46): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592375 | ||||||
chr1:2592378
|
A | AC | 6 | a0001c0001t0001g0199a0001c0001t0002g0031a0001c0001t0002g0192others(3): Show | 6 | HG00597.hp2 HG01099.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2067+276dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592378 | ||||||
chr1:2592378
|
ACCCCCTC others(223): Show |
A | 111 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(108): Show | 147 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.2067+47_2067+276de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592378 | ||||||
chr1:2592379
|
C | T | 47 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0135others(44): Show | 51 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.2067+276G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592379 | ||||||
chr1:2592379
|
CCCCCTCC others(222): Show |
C | 5 | a0002c0002t0001g0058a0002c0002t0003g0034a0002c0002t0003g0084others(2): Show | 5 | HG02080.hp2 HG03490.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+47_2067+275de others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592379 | ||||||
chr1:2592415
|
T | G | 8 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(5): Show | 11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+240A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592415 | ||||||
chr1:2592420
|
T | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+235A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592420 | ||||||
chr1:2592421
|
G | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+234C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592421 | ||||||
chr1:2592423
|
C | T | 8 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(5): Show | 11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+232G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592423 | ||||||
chr1:2592424
|
G | C | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+231C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592424 | ||||||
chr1:2592424
|
G | GC | 6 | a0001c0001t0002g0221a0002c0003t0001g0013a0002c0003t0001g0028others(3): Show | 9 | HG01123.hp1 HG01192.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2067+230dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592424 | ||||||
chr1:2592425
|
CCCCCTCC others(84): Show |
C | 3 | a0002c0008t0001g0049a0002c0008t0001g0050a0006c0009t0004g0277 | 3 | HG02280.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+139_2067+229d others(93): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592425 | ||||||
chr1:2592438
|
C | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+217G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592438 | ||||||
chr1:2592439
|
A | G | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+216T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592439 | ||||||
chr1:2592440
|
T | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+215A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592440 | ||||||
chr1:2592445
|
A | ATG | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+209_2067+210i others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592445 | ||||||
chr1:2592447
|
G | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+208C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592447 | ||||||
chr1:2592461
|
C | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+194G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592461 | ||||||
chr1:2592461
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.2067+194G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592461 | ||||||
chr1:2592462
|
G | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+193C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592462 | ||||||
chr1:2592463
|
T | C | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+192A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592463 | ||||||
chr1:2592468
|
G | A | 7 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(4): Show | 11 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+187C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592468 | ||||||
chr1:2592468
|
GCGCCCCC others(16): Show |
G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2067+164_2067+186d others(25): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592468 | ||||||
chr1:2592469
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+186G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592469 | ||||||
chr1:2592470
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2067+185C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592470 | ||||||
chr1:2592472
|
CCCCTCCC others(37): Show |
C | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+139_2067+182d others(46): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592472 | ||||||
chr1:2592484
|
C | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+171G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592484 | ||||||
chr1:2592491
|
A | ATG | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+163_2067+164i others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592491 | ||||||
chr1:2592493
|
G | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+162C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592493 | ||||||
chr1:2592508
|
G | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+147C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592508 | ||||||
chr1:2592509
|
C | T | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+146G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592509 | ||||||
chr1:2592530
|
C | A | 3 | a0002c0008t0001g0049a0002c0008t0001g0050a0006c0009t0004g0277 | 3 | HG02280.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+125G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592530 | ||||||
chr1:2592530
|
C | T | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+125G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592530 | ||||||
chr1:2592531
|
G | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2067+124C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592531 | ||||||
chr1:2592532
|
C | T | 7 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(4): Show | 11 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+123G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592532 | ||||||
chr1:2592537
|
A | C | 1 | a0002c0003t0001g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+118T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592537 | ||||||
chr1:2592537
|
A | G | 4 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(1): Show | 7 | HG01123.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+118T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592537 | ||||||
chr1:2592538
|
T | A | 1 | a0002c0003t0001g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+117A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592538 | ||||||
chr1:2592538
|
T | C | 6 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(3): Show | 10 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2067+117A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592538 | ||||||
chr1:2592539
|
G | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(1): Show | 7 | HG01123.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+116C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592539 | ||||||
chr1:2592539
|
G | C | 1 | a0002c0003t0001g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2067+116C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592539 | ||||||
chr1:2592554
|
G | A | 3 | a0002c0008t0001g0049a0002c0008t0001g0050a0006c0009t0004g0277 | 3 | HG02280.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2067+101C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592554 | ||||||
chr1:2592555
|
T | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+100A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592555 | ||||||
chr1:2592560
|
G | A | 8 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(5): Show | 11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+95C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592560 | ||||||
chr1:2592561
|
C | T | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+94G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592561 | ||||||
chr1:2592575
|
A | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+80T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592575 | ||||||
chr1:2592576
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+79A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592576 | ||||||
chr1:2592576
|
T | G | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+79A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592576 | ||||||
chr1:2592578
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+77G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592578 | ||||||
chr1:2592579
|
A | G | 4 | a0001c0001t0002g0246a0001c0001t0002g0247a0002c0008t0001g0049others(1): Show | 4 | HG01168.hp2 HG02129.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+76T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592579 | ||||||
chr1:2592583
|
G | GT | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+71_2067+72ins others(1): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592583 | ||||||
chr1:2592584
|
C | G | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+71G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592584 | ||||||
chr1:2592585
|
A | AC | 11 | a0001c0001t0001g0143a0001c0001t0001g0164a0001c0001t0001g0198others(8): Show | 11 | HG00597.hp2 HG00735.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2067+69dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | ||||||
chr1:2592585
|
A | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+70T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | ||||||
chr1:2592585
|
A | G | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+70T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | ||||||
chr1:2592585
|
ACCCCCTC others(16): Show |
A | 6 | a0002c0002t0001g0060a0002c0002t0001g0095a0002c0002t0003g0085others(3): Show | 6 | HG02083.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2067+47_2067+69del others(23): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592585 | ||||||
chr1:2592598
|
C | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+57G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592598 | ||||||
chr1:2592599
|
C | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+56G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592599 | ||||||
chr1:2592599
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+56G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592599 | ||||||
chr1:2592602
|
G | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+53C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592602 | ||||||
chr1:2592606
|
A | ATGCCCCC others(41): Show |
5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2067+48_2067+49ins others(48): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592606 | ||||||
chr1:2592606
|
A | G | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2067+49T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592606 | ||||||
chr1:2592608
|
G | A | 7 | a0001c0001t0002g0246a0001c0001t0002g0247a0002c0003t0001g0013others(4): Show | 10 | HG01123.hp1 HG01168.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2067+47C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 21/23 | chr1 | 2592608 | ||||||
chr1:2592725
|
G | A | 3 | a0002c0002t0001g0113a0002c0008t0001g0049a0002c0008t0001g0050 | 3 | HG02280.hp2 HG06807.hp1 NA18943.hp1 |
splice_region_variant&intron_variant | LOW | c.2002-5C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 20/23 | chr1 | 2592725 | ||||||
chr1:2592766
|
C | T | 119 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(116): Show | 155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2002-46G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 20/23 | chr1 | 2592766 | ||||||
chr1:2592803
|
C | T | 7 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(4): Show | 10 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2001+30G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 20/23 | chr1 | 2592803 | ||||||
chr1:2593018
|
T | C | 129 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(126): Show | 169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1868-52A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593018 | ||||||
chr1:2593046
|
C | T | 67 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0016others(64): Show | 88 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1868-80G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593046 | ||||||
chr1:2593057
|
C | T | 1 | a0002c0002t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1868-91G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593057 | ||||||
chr1:2593347
|
G | A | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1868-381C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593347 | ||||||
chr1:2593402
|
C | T | 1 | a0002c0002t0001g0021 | 2 | HG01070.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1867+412G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593402 | ||||||
chr1:2593456
|
G | C | 56 | a0002c0002t0001g0003a0002c0002t0001g0009a0002c0002t0001g0017others(53): Show | 74 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1867+358C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593456 | ||||||
chr1:2593476
|
G | T | 119 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(116): Show | 155 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1867+338C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593476 | ||||||
chr1:2593504
|
G | A | 129 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(126): Show | 169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1867+310C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593504 | ||||||
chr1:2593527
|
C | T | 126 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(123): Show | 165 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.1867+287G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593527 | ||||||
chr1:2593573
|
G | A | 1 | a0002c0008t0001g0049 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1867+241C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593573 | ||||||
chr1:2593631
|
C | T | 3 | a0002c0003t0001g0023a0002c0003t0006g0131a0006c0009t0004g0277 | 4 | HG00140.hp2 HG02965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1867+183G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593631 | ||||||
chr1:2593713
|
T | C | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1867+101A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593713 | ||||||
chr1:2593725
|
G | A | 7 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(4): Show | 10 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1867+89C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593725 | ||||||
chr1:2593769
|
C | T | 3 | a0002c0003t0001g0023a0002c0003t0006g0131a0006c0009t0004g0277 | 4 | HG00140.hp2 HG02965.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1867+45G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 19/23 | chr1 | 2593769 | ||||||
chr1:2594084
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1748-151G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 18/23 | chr1 | 2594084 | ||||||
chr1:2594221
|
G | A | 112 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(109): Show | 148 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1747+164C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 18/23 | chr1 | 2594221 | ||||||
chr1:2594226
|
T | C | 129 | a0001c0005t0001g0062a0002c0002t0001g0003a0002c0002t0001g0005others(126): Show | 169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1747+159A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 18/23 | chr1 | 2594226 | ||||||
chr1:2594533
|
G | T | 1 | a0002c0002t0001g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1689-90C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594533 | ||||||
chr1:2594569
|
A | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0166others(1): Show | 4 | NA18956.hp2 NA18974.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-126T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594569 | ||||||
chr1:2594752
|
G | GC | 22 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0149others(19): Show | 22 | HG00597.hp2 HG00741.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1688+37dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594752 | ||||||
chr1:2594761
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1688+29C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 17/23 | chr1 | 2594761 | ||||||
chr1:2594897
|
C | T | 4 | a0002c0002t0001g0047a0002c0002t0001g0058a0002c0002t0001g0063others(1): Show | 4 | HG02922.hp1 HG03130.hp1 HG03225.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1585-4G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2594897 | ||||||
chr1:2594913
|
A | G | 1 | a0005c0010t0001g0241 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1585-20T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2594913 | ||||||
chr1:2595006
|
G | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585-113C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595006 | ||||||
chr1:2595019
|
TG | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1585-127delC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595019 | ||||||
chr1:2595084
|
G | A | 2 | a0002c0002t0001g0051a0002c0002t0001g0052 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1585-191C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595084 | ||||||
chr1:2595098
|
C | T | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1584+178G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595098 | ||||||
chr1:2595132
|
G | A | 16 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0003g0004others(13): Show | 22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1584+144C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595132 | ||||||
chr1:2595182
|
G | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1584+94C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595182 | ||||||
chr1:2595236
|
C | T | 1 | a0001c0001t0007g0218 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1584+40G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 16/23 | chr1 | 2595236 | ||||||
chr1:2595423
|
G | A | 1 | a0001c0005t0001g0062 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1501-64C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595423 | ||||||
chr1:2595497
|
G | A | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1501-138C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595497 | ||||||
chr1:2595741
|
C | G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1500+268G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595741 | ||||||
chr1:2595805
|
T | TGGTCCTG others(33): Show |
6 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1500+164_1500+203d others(42): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595805 | ||||||
chr1:2595805
|
TGGTCCTG others(33): Show |
T | 10 | a0001c0001t0001g0165a0002c0003t0001g0013a0002c0003t0001g0023others(7): Show | 14 | HG00140.hp2 HG01106.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1500+164_1500+203d others(42): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595805 | ||||||
chr1:2595864
|
C | A | 1 | a0002c0003t0001g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1500+145G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595864 | ||||||
chr1:2595891
|
T | C | 1 | a0002c0002t0001g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1500+118A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595891 | ||||||
chr1:2595904
|
C | T | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1500+105G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595904 | ||||||
chr1:2595931
|
G | A | 1 | a0002c0004t0001g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1500+78C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 15/23 | chr1 | 2595931 | ||||||
chr1:2596239
|
A | G | 161 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(158): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1402-132T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596239 | ||||||
chr1:2596255
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1402-148G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596255 | ||||||
chr1:2596391
|
C | T | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1401+170G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596391 | ||||||
chr1:2596420
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1401+141G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596420 | ||||||
chr1:2596462
|
TG | T | 10 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0034others(7): Show | 15 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1401+98delC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 14/23 | chr1 | 2596462 | ||||||
chr1:2596694
|
T | C | 162 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(159): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
splice_region_variant&intron_variant | LOW | c.1273-5A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596694 | ||||||
chr1:2596705
|
G | A | 1 | a0003c0006t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1273-16C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596705 | ||||||
chr1:2596858
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1273-169C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596858 | ||||||
chr1:2596901
|
C | A | 11 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(8): Show | 17 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1273-212G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2596901 | ||||||
chr1:2597132
|
TC | T | 2 | a0002c0002t0001g0010a0008c0011t0001g0128 | 4 | HG01109.hp2 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273-444delG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597132 | ||||||
chr1:2597240
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0253 | 2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1273-551G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597240 | ||||||
chr1:2597243
|
T | C | 159 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(156): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1273-554A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597243 | ||||||
chr1:2597304
|
C | G | 1 | a0002c0002t0001g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1273-615G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597304 | ||||||
chr1:2597336
|
C | A | 13 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(10): Show | 19 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1273-647G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597336 | ||||||
chr1:2597494
|
C | T | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272+713G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597494 | ||||||
chr1:2597513
|
G | A | 1 | a0002c0002t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1272+694C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597513 | ||||||
chr1:2597560
|
G | T | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1272+647C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597560 | ||||||
chr1:2597658
|
T | C | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1272+549A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597658 | ||||||
chr1:2597718
|
C | A | 4 | a0002c0002t0003g0066a0002c0002t0003g0068a0002c0002t0003g0083others(1): Show | 4 | NA18970.hp1 NA18984.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+489G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597718 | ||||||
chr1:2597753
|
A | G | 161 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(158): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1272+454T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597753 | ||||||
chr1:2597829
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1272+378G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597829 | ||||||
chr1:2597842
|
G | A | 2 | a0001c0001t0002g0229a0001c0001t0007g0218 | 2 | HG02080.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1272+365C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597842 | ||||||
chr1:2597844
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1272+363C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597844 | ||||||
chr1:2597921
|
G | A | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1272+286C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597921 | ||||||
chr1:2597960
|
G | T | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1272+247C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597960 | ||||||
chr1:2597998
|
C | T | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1272+209G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2597998 | ||||||
chr1:2598078
|
C | T | 1 | a0002c0002t0003g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1272+129G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2598078 | ||||||
chr1:2598113
|
G | A | 14 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1272+94C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2598113 | ||||||
chr1:2598124
|
G | A | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1272+83C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 13/23 | chr1 | 2598124 | ||||||
chr1:2598806
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1042-16C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598806 | ||||||
chr1:2598820
|
G | GGA | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1042-32_1042-31dup others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598820 | ||||||
chr1:2598856
|
T | C | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1042-66A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598856 | ||||||
chr1:2598902
|
A | AG | 163 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(160): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1042-113dupC | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598902 | ||||||
chr1:2598972
|
C | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1042-182G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2598972 | ||||||
chr1:2599035
|
A | G | 1 | a0001c0001t0007g0218 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1042-245T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599035 | ||||||
chr1:2599119
|
T | C | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-329A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599119 | ||||||
chr1:2599255
|
G | A | 163 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(160): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1042-465C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599255 | ||||||
chr1:2599455
|
C | A | 1 | a0002c0002t0001g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1042-665G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599455 | ||||||
chr1:2599723
|
T | G | 1 | a0002c0017t0001g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1042-933A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599723 | ||||||
chr1:2599772
|
G | A | 1 | a0002c0003t0006g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1042-982C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599772 | ||||||
chr1:2599856
|
C | CAA | 17 | a0001c0001t0001g0135a0001c0001t0001g0145a0001c0001t0001g0150others(14): Show | 20 | HG01106.hp1 HG01106.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1042-1068_1042-106 others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599856 | ||||||
chr1:2599856
|
C | CAAA | 137 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(134): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1042-1069_1042-106 others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599856 | ||||||
chr1:2599933
|
A | C | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-1143T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2599933 | ||||||
chr1:2600028
|
T | C | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-1238A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600028 | ||||||
chr1:2600066
|
C | T | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1042-1276G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600066 | ||||||
chr1:2600075
|
C | A | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-1285G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600075 | ||||||
chr1:2600297
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1042-1507C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600297 | ||||||
chr1:2600334
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1042-1544T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600334 | ||||||
chr1:2600536
|
GAA | G | 9 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(6): Show | 13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-1748_1042-174 others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600536 | ||||||
chr1:2600536
|
GAAA | G | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1042-1749_1042-174 others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600536 | ||||||
chr1:2600539
|
A | G | 9 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(6): Show | 13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-1749T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600539 | ||||||
chr1:2600540
|
A | G | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1042-1750T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600540 | ||||||
chr1:2600541
|
A | G | 39 | a0001c0005t0001g0062a0002c0002t0001g0005a0002c0002t0001g0007others(36): Show | 54 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1042-1751T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600541 | ||||||
chr1:2600570
|
G | T | 1 | a0002c0002t0001g0101 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1042-1780C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600570 | ||||||
chr1:2600607
|
G | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042-1817C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600607 | ||||||
chr1:2600642
|
T | C | 1 | a0002c0002t0001g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1042-1852A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600642 | ||||||
chr1:2600684
|
T | TCAAACAA others(5): Show |
1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1042-1906_1042-189 others(16): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600684 | ||||||
chr1:2600684
|
TCAAACAA others(5): Show |
T | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-1906_1042-189 others(16): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600684 | ||||||
chr1:2600720
|
C | CTGT | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-1933_1042-193 others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600720 | ||||||
chr1:2600977
|
T | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(160): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1042-2187A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2600977 | ||||||
chr1:2601001
|
A | T | 1 | a0002c0017t0001g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1042-2211T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601001 | ||||||
chr1:2601014
|
C | CT | 163 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(160): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1042-2225dupA | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601014 | ||||||
chr1:2601040
|
A | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG02896.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1042-2250T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601040 | ||||||
chr1:2601067
|
G | A | 162 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(159): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1042-2277C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601067 | ||||||
chr1:2601088
|
G | A | 9 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(6): Show | 13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-2298C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601088 | ||||||
chr1:2601185
|
C | T | 160 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(157): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1042-2395G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601185 | ||||||
chr1:2601222
|
T | A | 1 | a0002c0008t0001g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1042-2432A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601222 | ||||||
chr1:2601348
|
C | A | 1 | a0002c0002t0001g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1041+2536G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601348 | ||||||
chr1:2601460
|
C | A | 161 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(158): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1041+2424G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601460 | ||||||
chr1:2601582
|
T | G | 1 | a0002c0017t0001g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1041+2302A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601582 | ||||||
chr1:2601669
|
C | T | 3 | a0002c0002t0001g0054a0002c0002t0001g0081a0002c0002t0001g0090 | 3 | NA18952.hp1 NA18960.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1041+2215G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601669 | ||||||
chr1:2601726
|
G | A | 9 | a0001c0001t0001g0158a0002c0004t0001g0267a0002c0004t0001g0268others(6): Show | 9 | HG02055.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+2158C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601726 | ||||||
chr1:2601786
|
T | C | 1 | a0002c0002t0001g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1041+2098A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601786 | ||||||
chr1:2601811
|
C | A | 120 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(117): Show | 156 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.1041+2073G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601811 | ||||||
chr1:2601902
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1041+1982G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601902 | ||||||
chr1:2601963
|
CAG | C | 11 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(8): Show | 15 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1041+1919_1041+192 others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2601963 | ||||||
chr1:2602003
|
CAGCAATT others(64): Show |
C | 1 | a0001c0021t0001g0159 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1041+1810_1041+188 others(75): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602003 | ||||||
chr1:2602113
|
A | C | 121 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(118): Show | 157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+1771T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602113 | ||||||
chr1:2602115
|
G | GTTCTTAG others(73): Show |
121 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(118): Show | 157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+1768_1041+176 others(84): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602115 | ||||||
chr1:2602166
|
G | A | 113 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(110): Show | 149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1041+1718C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602166 | ||||||
chr1:2602257
|
C | T | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1041+1627G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602257 | ||||||
chr1:2602258
|
G | A | 1 | a0006c0009t0004g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+1626C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602258 | ||||||
chr1:2602267
|
G | A | 121 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(118): Show | 157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+1617C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602267 | ||||||
chr1:2602312
|
G | GGGCGATT others(29): Show |
1 | a0002c0017t0001g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1041+1536_1041+157 others(40): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602312 | ||||||
chr1:2602328
|
C | T | 6 | a0002c0002t0001g0017a0002c0002t0001g0054a0002c0002t0001g0067others(3): Show | 7 | NA18952.hp1 NA18955.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+1556G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602328 | ||||||
chr1:2602393
|
G | A | 2 | a0005c0010t0001g0236a0005c0010t0001g0241 | 2 | HG00323.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1041+1491C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602393 | ||||||
chr1:2602648
|
C | T | 113 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(110): Show | 149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1041+1236G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602648 | ||||||
chr1:2602683
|
C | T | 3 | a0001c0001t0002g0191a0001c0001t0002g0208a0001c0001t0002g0210 | 3 | HG01175.hp2 HG01256.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1041+1201G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602683 | ||||||
chr1:2602738
|
C | T | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1146G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602738 | ||||||
chr1:2602758
|
T | C | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+1126A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602758 | ||||||
chr1:2602808
|
G | C | 11 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(8): Show | 15 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1041+1076C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602808 | ||||||
chr1:2602866
|
AGCTCATC others(19): Show |
A | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+992_1041+1017 others(29): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602866 | ||||||
chr1:2602894
|
T | A | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+990A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602894 | ||||||
chr1:2602895
|
GA | G | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+988delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602895 | ||||||
chr1:2602936
|
G | A | 15 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0003g0004others(12): Show | 21 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1041+948C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602936 | ||||||
chr1:2602947
|
T | A | 7 | a0001c0005t0001g0062a0002c0002t0001g0010a0002c0002t0001g0022others(4): Show | 10 | HG00642.hp2 HG01109.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1041+937A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602947 | ||||||
chr1:2602948
|
C | A | 7 | a0001c0005t0001g0062a0002c0002t0001g0010a0002c0002t0001g0022others(4): Show | 10 | HG00642.hp2 HG01109.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1041+936G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2602948 | ||||||
chr1:2603033
|
G | A | 2 | a0002c0002t0003g0089a0002c0002t0003g0122 | 2 | HG00597.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1041+851C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603033 | ||||||
chr1:2603289
|
C | T | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+595G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603289 | ||||||
chr1:2603362
|
G | C | 121 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(118): Show | 157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1041+522C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603362 | ||||||
chr1:2603513
|
C | A | 1 | a0002c0002t0001g0020 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1041+371G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603513 | ||||||
chr1:2603539
|
G | A | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1041+345C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603539 | ||||||
chr1:2603653
|
ACT | A | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1041+229_1041+230d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603653 | ||||||
chr1:2603763
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0166 | 3 | NA18974.hp1 NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1041+121C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603763 | ||||||
chr1:2603836
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+48G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 11/23 | chr1 | 2603836 | ||||||
chr1:2604001
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.952-28G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/23 | chr1 | 2604001 | ||||||
chr1:2604057
|
C | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 12 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.952-84G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/23 | chr1 | 2604057 | ||||||
chr1:2604130
|
C | A | 7 | a0002c0002t0001g0005a0002c0002t0001g0041a0002c0002t0001g0043others(4): Show | 10 | HG01099.hp1 HG01261.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.951+17G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 10/23 | chr1 | 2604130 | ||||||
chr1:2604318
|
C | T | 1 | a0001c0005t0001g0062 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.817-37G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604318 | ||||||
chr1:2604319
|
A | G | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.817-38T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604319 | ||||||
chr1:2604445
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.817-164G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604445 | ||||||
chr1:2604454
|
C | T | 1 | a0002c0004t0001g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.817-173G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604454 | ||||||
chr1:2604456
|
C | T | 119 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(116): Show | 155 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.817-175G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604456 | ||||||
chr1:2604482
|
G | A | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-201C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604482 | ||||||
chr1:2604563
|
C | G | 121 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(118): Show | 157 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.817-282G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2604563 | ||||||
chr1:2605117
|
C | T | 1 | a0002c0002t0003g0080 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.816+441G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605117 | ||||||
chr1:2605205
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816+353C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605205 | ||||||
chr1:2605374
|
C | A | 13 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(10): Show | 19 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.816+184G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605374 | ||||||
chr1:2605406
|
C | T | 9 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(6): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.816+152G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605406 | ||||||
chr1:2605459
|
G | C | 2 | a0004c0007t0001g0029a0013c0019t0001g0271 | 3 | HG02976.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.816+99C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 9/23 | chr1 | 2605459 | ||||||
chr1:2605633
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0156a0001c0001t0001g0252others(5): Show | 9 | HG00738.hp1 HG01515.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.751-10G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605633 | ||||||
chr1:2605656
|
G | A | 120 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(117): Show | 158 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.751-33C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605656 | ||||||
chr1:2605727
|
A | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.751-104T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605727 | ||||||
chr1:2605790
|
C | T | 7 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(4): Show | 11 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.751-167G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605790 | ||||||
chr1:2605974
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.750+274G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2605974 | ||||||
chr1:2606025
|
A | G | 133 | a0001c0001t0002g0209a0001c0005t0001g0062a0001c0005t0001g0082others(130): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.750+223T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2606025 | ||||||
chr1:2606104
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.750+144G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 8/23 | chr1 | 2606104 | ||||||
chr1:2606399
|
C | T | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.632-33G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606399 | ||||||
chr1:2606550
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.632-184C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606550 | ||||||
chr1:2606566
|
G | A | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.632-200C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606566 | ||||||
chr1:2606570
|
G | A | 1 | a0002c0002t0003g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.632-204C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606570 | ||||||
chr1:2606685
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.631+289G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606685 | ||||||
chr1:2606770
|
G | A | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.631+204C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606770 | ||||||
chr1:2606828
|
C | T | 1 | a0002c0003t0001g0278 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.631+146G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606828 | ||||||
chr1:2606905
|
A | G | 18 | a0002c0003t0001g0013a0002c0003t0001g0023a0002c0003t0001g0028others(15): Show | 23 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.631+69T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606905 | ||||||
chr1:2606910
|
G | A | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.631+64C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606910 | ||||||
chr1:2606941
|
T | G | 1 | a0002c0002t0001g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.631+33A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 7/23 | chr1 | 2606941 | ||||||
chr1:2607081
|
C | T | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.536-12G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607081 | ||||||
chr1:2607136
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.536-67A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607136 | ||||||
chr1:2607143
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.536-74C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607143 | ||||||
chr1:2607196
|
C | T | 1 | a0002c0002t0003g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.536-127G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607196 | ||||||
chr1:2607267
|
C | T | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.536-198G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607267 | ||||||
chr1:2607299
|
C | T | 11 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(8): Show | 17 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.536-230G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607299 | ||||||
chr1:2607387
|
C | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.536-318G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607387 | ||||||
chr1:2607447
|
G | T | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.536-378C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607447 | ||||||
chr1:2607532
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.536-463G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607532 | ||||||
chr1:2607567
|
T | C | 130 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(127): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-498A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607567 | ||||||
chr1:2607742
|
C | T | 130 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(127): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-673G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607742 | ||||||
chr1:2607784
|
C | T | 1 | a0002c0002t0003g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.536-715G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607784 | ||||||
chr1:2607790
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.536-721G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607790 | ||||||
chr1:2607830
|
T | G | 1 | a0002c0003t0001g0023 | 2 | NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.536-761A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607830 | ||||||
chr1:2607961
|
T | C | 116 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(113): Show | 152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.536-892A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2607961 | ||||||
chr1:2608093
|
A | G | 130 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(127): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-1024T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608093 | ||||||
chr1:2608116
|
A | G | 130 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(127): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.536-1047T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608116 | ||||||
chr1:2608151
|
C | T | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.536-1082G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608151 | ||||||
chr1:2608164
|
G | A | 114 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(111): Show | 149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.536-1095C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608164 | ||||||
chr1:2608172
|
C | T | 1 | a0002c0002t0001g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.536-1103G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608172 | ||||||
chr1:2608220
|
G | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.535+1119C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608220 | ||||||
chr1:2608235
|
C | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.535+1104G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608235 | ||||||
chr1:2608357
|
C | T | 114 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(111): Show | 149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.535+982G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608357 | ||||||
chr1:2608389
|
T | C | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.535+950A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608389 | ||||||
chr1:2608462
|
A | C | 130 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(127): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.535+877T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608462 | ||||||
chr1:2608507
|
CAT | C | 114 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(111): Show | 149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.535+830_535+831del others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608507 | ||||||
chr1:2608542
|
CACAT | C | 114 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(111): Show | 149 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.535+793_535+796del others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608542 | ||||||
chr1:2608790
|
G | A | 1 | a0002c0002t0003g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.535+549C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608790 | ||||||
chr1:2608823
|
C | T | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.535+516G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608823 | ||||||
chr1:2608838
|
A | G | 1 | a0002c0002t0003g0078 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.535+501T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608838 | ||||||
chr1:2608860
|
T | C | 1 | a0001c0001t0002g0216 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.535+479A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608860 | ||||||
chr1:2608904
|
A | C | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.535+435T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608904 | ||||||
chr1:2608906
|
C | CACATAT | 187 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0135others(184): Show | 231 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.535+427_535+432dup others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608906 | ||||||
chr1:2608925
|
G | A | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.535+414C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608925 | ||||||
chr1:2608932
|
C | A | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.535+407G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2608932 | ||||||
chr1:2609034
|
T | TAC | 12 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0143others(9): Show | 12 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+303_535+304dup others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
T | TACAC | 15 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0135others(12): Show | 19 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.535+301_535+304dup others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
T | TACACAC | 14 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0149others(11): Show | 14 | HG00544.hp2 HG00609.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.535+299_535+304dup others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0171 | 2 | HG02109.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.535+295_535+304dup others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TAC | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0130a0001c0001t0001g0140others(23): Show | 29 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.535+303_535+304del others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACAC | T | 50 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0184others(47): Show | 65 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.535+301_535+304del others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACAC | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0181a0001c0001t0002g0208others(2): Show | 6 | HG00140.hp1 HG00639.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+299_535+304del others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACACA others(3): Show |
T | 3 | a0002c0002t0001g0093a0002c0002t0001g0094a0002c0003t0001g0023 | 4 | HG02273.hp2 HG02451.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+295_535+304del others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACACA others(5): Show |
T | 15 | a0001c0005t0001g0092a0002c0002t0001g0003a0002c0002t0001g0019others(12): Show | 21 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.535+293_535+304del others(12): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACACA others(7): Show |
T | 96 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0014t0002g0120others(93): Show | 125 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.535+291_535+304del others(14): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACACA others(9): Show |
T | 8 | a0002c0002t0001g0118a0002c0003t0001g0013a0002c0003t0001g0028others(5): Show | 11 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.535+289_535+304del others(16): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACACA others(11): Show |
T | 2 | a0002c0012t0001g0126a0011c0020t0001g0266 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.535+287_535+304del others(18): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609034
|
TACACACA others(13): Show |
T | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 8 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+285_535+304del others(20): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609034 | ||||||
chr1:2609155
|
T | G | 8 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+184A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609155 | ||||||
chr1:2609203
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.535+136G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 6/23 | chr1 | 2609203 | ||||||
chr1:2609473
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.455-54C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/23 | chr1 | 2609473 | ||||||
chr1:2609617
|
G | A | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.454+53C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 5/23 | chr1 | 2609617 | ||||||
chr1:2610117
|
T | C | 2 | a0002c0002t0001g0018a0002c0002t0001g0095 | 3 | HG02083.hp2 NA18951.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.293-286A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610117 | ||||||
chr1:2610220
|
T | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0255 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.293-389A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610220 | ||||||
chr1:2610288
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 12 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-457G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610288 | ||||||
chr1:2610365
|
C | T | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.293-534G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610365 | ||||||
chr1:2610502
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.293-671G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610502 | ||||||
chr1:2610533
|
G | C | 1 | a0002c0016t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.293-702C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610533 | ||||||
chr1:2610724
|
A | AC | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+556dupG | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610724 | ||||||
chr1:2610936
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0064a0002c0002t0001g0108 | 4 | HG00642.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+345T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2610936 | ||||||
chr1:2611053
|
T | G | 1 | a0002c0002t0003g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.292+228A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611053 | ||||||
chr1:2611060
|
C | T | 1 | a0002c0003t0001g0280 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292+221G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611060 | ||||||
chr1:2611080
|
G | A | 1 | a0012c0013t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.292+201C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611080 | ||||||
chr1:2611199
|
C | T | 1 | a0002c0002t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.292+82G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611199 | ||||||
chr1:2611214
|
A | G | 134 | a0001c0001t0001g0130a0001c0001t0005g0030a0001c0005t0001g0062others(131): Show | 174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.292+67T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 4/23 | chr1 | 2611214 | ||||||
chr1:2611372
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.233-32C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611372 | ||||||
chr1:2611415
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233-75C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611415 | ||||||
chr1:2611423
|
TGGTGGGT others(46): Show |
T | 1 | a0002c0004t0001g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233-136_233-84delC others(52): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611423 | ||||||
chr1:2611444
|
G | A | 1 | a0012c0013t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.233-104C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611444 | ||||||
chr1:2611799
|
C | T | 1 | a0002c0002t0001g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.232+328G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611799 | ||||||
chr1:2611862
|
G | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.232+265C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611862 | ||||||
chr1:2611931
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.232+196T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2611931 | ||||||
chr1:2612072
|
G | A | 2 | a0002c0002t0001g0056a0002c0002t0001g0098 | 2 | HG00099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.232+55C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 3/23 | chr1 | 2612072 | ||||||
chr1:2612352
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.155-148C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612352 | ||||||
chr1:2612379
|
C | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0207 | 3 | NA19007.hp1 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.155-175G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612379 | ||||||
chr1:2612436
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155-232G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612436 | ||||||
chr1:2612743
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.155-539C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2612743 | ||||||
chr1:2613200
|
C | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0207 | 3 | NA19007.hp1 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.155-996G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613200 | ||||||
chr1:2613201
|
G | A | 111 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(108): Show | 146 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.155-997C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613201 | ||||||
chr1:2613208
|
G | A | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.155-1004C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613208 | ||||||
chr1:2613567
|
G | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-1363C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613567 | ||||||
chr1:2613649
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0265 | 3 | HG00738.hp1 HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.155-1445G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613649 | ||||||
chr1:2613830
|
G | C | 16 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(13): Show | 20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-1626C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613830 | ||||||
chr1:2613977
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.155-1773C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2613977 | ||||||
chr1:2614215
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.155-2011G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614215 | ||||||
chr1:2614346
|
C | T | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.155-2142G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614346 | ||||||
chr1:2614394
|
C | T | 16 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(13): Show | 20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-2190G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614394 | ||||||
chr1:2614650
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155-2446G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614650 | ||||||
chr1:2614790
|
G | A | 114 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(111): Show | 149 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.155-2586C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614790 | ||||||
chr1:2614852
|
C | T | 11 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0255others(8): Show | 11 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-2648G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614852 | ||||||
chr1:2614904
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155-2700G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614904 | ||||||
chr1:2614906
|
C | A | 2 | a0001c0001t0001g0195a0002c0002t0003g0035 | 2 | HG01358.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155-2702G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2614906 | ||||||
chr1:2615007
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.155-2803G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615007 | ||||||
chr1:2615039
|
A | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0064a0002c0002t0001g0108 | 4 | HG00642.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-2835T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615039 | ||||||
chr1:2615121
|
T | C | 1 | a0002c0002t0001g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.155-2917A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615121 | ||||||
chr1:2615154
|
G | A | 4 | a0002c0002t0001g0019a0002c0002t0001g0055a0002c0002t0001g0056others(1): Show | 5 | HG00099.hp1 HG00639.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-2950C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615154 | ||||||
chr1:2615322
|
G | C | 1 | a0002c0002t0003g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.155-3118C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615322 | ||||||
chr1:2615369
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.155-3165A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615369 | ||||||
chr1:2615568
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.155-3364C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615568 | ||||||
chr1:2615712
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.155-3508G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615712 | ||||||
chr1:2615772
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01256.hp1 HG02683.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.155-3568C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615772 | ||||||
chr1:2615819
|
A | G | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-3615T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615819 | ||||||
chr1:2615838
|
A | T | 4 | a0002c0002t0001g0073a0002c0002t0001g0076a0002c0002t0001g0113others(1): Show | 4 | NA18943.hp1 NA18982.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-3634T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615838 | ||||||
chr1:2615855
|
C | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-3651G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2615855 | ||||||
chr1:2616028
|
C | T | 5 | a0002c0002t0001g0007a0002c0002t0001g0057a0002c0002t0001g0061others(2): Show | 7 | HG01891.hp2 HG02886.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-3824G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616028 | ||||||
chr1:2616121
|
A | T | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.155-3917T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616121 | ||||||
chr1:2616170
|
A | G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155-3966T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616170 | ||||||
chr1:2616342
|
C | CA | 16 | a0001c0001t0002g0232a0001c0005t0001g0062a0002c0002t0001g0045others(13): Show | 16 | HG00140.hp2 HG00741.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.155-4139dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | ||||||
chr1:2616342
|
C | CAA | 100 | a0001c0005t0001g0082a0001c0005t0001g0092a0001c0014t0002g0120others(97): Show | 135 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.155-4140_155-4139d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | ||||||
chr1:2616342
|
C | CAAAA | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-4142_155-4139d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | ||||||
chr1:2616342
|
C | CAAAAA | 6 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(3): Show | 9 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.155-4143_155-4139d others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | ||||||
chr1:2616342
|
CA | C | 12 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0001g0169others(9): Show | 13 | HG00280.hp2 HG01070.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.155-4139delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616342 | ||||||
chr1:2616410
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155-4206G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616410 | ||||||
chr1:2616522
|
A | G | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.155-4318T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616522 | ||||||
chr1:2616589
|
A | G | 280 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(277): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.155-4385T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616589 | ||||||
chr1:2616712
|
A | C | 1 | a0002c0002t0003g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.155-4508T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616712 | ||||||
chr1:2616802
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02723.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-4598G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616802 | ||||||
chr1:2616849
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.155-4645G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616849 | ||||||
chr1:2616910
|
C | G | 1 | a0006c0009t0004g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.155-4706G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616910 | ||||||
chr1:2616944
|
T | G | 2 | a0002c0002t0001g0043a0002c0002t0001g0044 | 2 | HG01261.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.155-4740A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2616944 | ||||||
chr1:2617228
|
C | T | 1 | a0002c0002t0001g0101 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.155-5024G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617228 | ||||||
chr1:2617234
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.155-5030G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617234 | ||||||
chr1:2617238
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.155-5034A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617238 | ||||||
chr1:2617299
|
C | T | 2 | a0002c0002t0003g0032a0002c0002t0003g0033 | 2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.155-5095G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617299 | ||||||
chr1:2617336
|
A | G | 1 | a0002c0012t0001g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.155-5132T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617336 | ||||||
chr1:2617344
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.155-5140C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617344 | ||||||
chr1:2617381
|
C | T | 4 | a0002c0002t0001g0016a0002c0002t0001g0047a0002c0002t0001g0069others(1): Show | 5 | HG02280.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-5177G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617381 | ||||||
chr1:2617382
|
G | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02723.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-5178C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617382 | ||||||
chr1:2617383
|
C | T | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.155-5179G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617383 | ||||||
chr1:2617413
|
A | C | 131 | a0001c0005t0001g0082a0001c0005t0001g0092a0001c0014t0002g0120others(128): Show | 171 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.155-5209T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617413 | ||||||
chr1:2617413
|
A | T | 1 | a0001c0005t0001g0062 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.155-5209T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617413 | ||||||
chr1:2617426
|
C | CA | 21 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0153others(18): Show | 21 | HG00733.hp1 HG00738.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-5223dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | ||||||
chr1:2617426
|
C | CAAAA | 5 | a0002c0003t0001g0028a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 6 | HG01123.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-5226_155-5223d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | ||||||
chr1:2617426
|
C | CAAAAA | 7 | a0002c0003t0001g0013a0002c0003t0001g0280a0002c0004t0001g0269others(4): Show | 9 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-5227_155-5223d others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | ||||||
chr1:2617426
|
CA | C | 102 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0145others(99): Show | 135 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.155-5223delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | ||||||
chr1:2617426
|
CAA | C | 16 | a0001c0001t0001g0168a0001c0001t0001g0174a0002c0002t0001g0007others(13): Show | 19 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.155-5224_155-5223d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617426 | ||||||
chr1:2617460
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.155-5256G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617460 | ||||||
chr1:2617461
|
G | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-5257C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617461 | ||||||
chr1:2617650
|
T | G | 16 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(13): Show | 20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-5446A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617650 | ||||||
chr1:2617710
|
A | G | 16 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(13): Show | 20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-5506T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617710 | ||||||
chr1:2617714
|
T | A | 1 | a0002c0002t0001g0020 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.155-5510A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617714 | ||||||
chr1:2617802
|
G | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-5598C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2617802 | ||||||
chr1:2618163
|
G | A | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.155-5959C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618163 | ||||||
chr1:2618178
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.155-5974A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618178 | ||||||
chr1:2618322
|
T | C | 1 | a0002c0002t0001g0021 | 2 | HG01070.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.155-6118A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618322 | ||||||
chr1:2618681
|
G | T | 1 | a0001c0001t0002g0204 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.155-6477C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618681 | ||||||
chr1:2618812
|
C | A | 1 | a0002c0002t0001g0100 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.155-6608G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618812 | ||||||
chr1:2618904
|
C | T | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.155-6700G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2618904 | ||||||
chr1:2619027
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.155-6823C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619027 | ||||||
chr1:2619197
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.155-6993A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619197 | ||||||
chr1:2619345
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.155-7141C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619345 | ||||||
chr1:2619352
|
A | G | 1 | a0002c0002t0003g0038 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.155-7148T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619352 | ||||||
chr1:2619503
|
C | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-7299G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619503 | ||||||
chr1:2619526
|
C | T | 16 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(13): Show | 20 | HG01123.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-7322G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619526 | ||||||
chr1:2619612
|
C | T | 1 | a0002c0002t0001g0111 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.155-7408G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619612 | ||||||
chr1:2619614
|
T | C | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.155-7410A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619614 | ||||||
chr1:2619655
|
CA | C | 132 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0130others(129): Show | 154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.155-7452delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | ||||||
chr1:2619655
|
CAA | C | 46 | a0001c0001t0001g0141a0001c0001t0001g0169a0001c0001t0001g0170others(43): Show | 62 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.155-7453_155-7452d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | ||||||
chr1:2619655
|
CAAA | C | 19 | a0001c0014t0002g0120a0002c0002t0001g0041a0002c0002t0001g0058others(16): Show | 20 | HG00140.hp2 HG02055.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.155-7454_155-7452d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | ||||||
chr1:2619655
|
CAAAA | C | 68 | a0001c0005t0001g0082a0001c0005t0001g0092a0002c0002t0001g0003others(65): Show | 89 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.155-7455_155-7452d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | ||||||
chr1:2619655
|
CAAAAA | C | 4 | a0002c0002t0003g0008a0002c0002t0003g0053a0002c0002t0003g0066others(1): Show | 6 | HG02523.hp2 NA18956.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-7456_155-7452d others(7): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619655 | ||||||
chr1:2619933
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.155-7729C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619933 | ||||||
chr1:2619989
|
T | C | 1 | a0002c0002t0001g0109 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.155-7785A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2619989 | ||||||
chr1:2620014
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.155-7810C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620014 | ||||||
chr1:2620221
|
T | G | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 147 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.155-8017A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620221 | ||||||
chr1:2620346
|
C | T | 46 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0135others(43): Show | 50 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.155-8142G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620346 | ||||||
chr1:2620461
|
G | A | 79 | a0001c0005t0001g0082a0001c0005t0001g0092a0002c0002t0001g0003others(76): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.155-8257C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620461 | ||||||
chr1:2620632
|
T | C | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.155-8428A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620632 | ||||||
chr1:2620778
|
G | GA | 142 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(139): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.154+8552dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620778 | ||||||
chr1:2620778
|
G | GAA | 113 | a0001c0001t0001g0145a0001c0001t0001g0167a0001c0001t0001g0168others(110): Show | 148 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.154+8551_154+8552d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620778 | ||||||
chr1:2620778
|
G | GAAA | 9 | a0002c0002t0001g0101a0002c0002t0001g0102a0002c0002t0001g0103others(6): Show | 9 | HG01975.hp2 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+8550_154+8552d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2620778 | ||||||
chr1:2621383
|
G | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+7948C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621383 | ||||||
chr1:2621392
|
A | G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+7939T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621392 | ||||||
chr1:2621572
|
A | AT | 104 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(101): Show | 137 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.154+7758dupA | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621572 | ||||||
chr1:2621572
|
A | ATT | 8 | a0002c0002t0001g0005a0002c0002t0001g0041a0002c0002t0001g0043others(5): Show | 11 | HG01099.hp1 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+7757_154+7758d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621572 | ||||||
chr1:2621626
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.154+7705G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621626 | ||||||
chr1:2621644
|
G | A | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+7687C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621644 | ||||||
chr1:2621652
|
C | T | 1 | a0002c0002t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.154+7679G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621652 | ||||||
chr1:2621712
|
C | T | 1 | a0002c0002t0001g0054 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.154+7619G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621712 | ||||||
chr1:2621829
|
T | C | 1 | a0002c0002t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+7502A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621829 | ||||||
chr1:2621943
|
C | T | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+7388G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2621943 | ||||||
chr1:2622055
|
G | A | 8 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+7276C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622055 | ||||||
chr1:2622103
|
TAGG | T | 124 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(121): Show | 164 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.154+7225_154+7227d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622103 | ||||||
chr1:2622185
|
T | C | 117 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(114): Show | 153 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.154+7146A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622185 | ||||||
chr1:2622218
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0138others(8): Show | 12 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+7113G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622218 | ||||||
chr1:2622312
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+7019G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622312 | ||||||
chr1:2622319
|
C | T | 132 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(129): Show | 172 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.154+7012G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622319 | ||||||
chr1:2622571
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.154+6760A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622571 | ||||||
chr1:2622606
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.154+6725G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622606 | ||||||
chr1:2622681
|
T | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0135a0001c0001t0001g0158others(10): Show | 16 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.154+6650A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622681 | ||||||
chr1:2622747
|
T | C | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+6584A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622747 | ||||||
chr1:2622815
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02717.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.154+6516G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622815 | ||||||
chr1:2622848
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154+6483G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622848 | ||||||
chr1:2622883
|
CA | C | 21 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0145others(18): Show | 21 | HG00597.hp2 HG01515.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.154+6447delT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | ||||||
chr1:2622883
|
CAA | C | 9 | a0002c0002t0001g0117a0002c0003t0001g0013a0002c0003t0001g0023others(6): Show | 13 | HG00140.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.154+6446_154+6447d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | ||||||
chr1:2622883
|
CAAA | C | 11 | a0002c0002t0001g0022a0002c0002t0001g0108a0002c0002t0001g0109others(8): Show | 12 | HG00438.hp1 HG00544.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+6445_154+6447d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | ||||||
chr1:2622883
|
CAAAA | C | 103 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(100): Show | 138 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.154+6444_154+6447d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622883 | ||||||
chr1:2622905
|
T | G | 122 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(119): Show | 161 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.154+6426A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2622905 | ||||||
chr1:2623124
|
A | G | 115 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(112): Show | 151 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.154+6207T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623124 | ||||||
chr1:2623164
|
T | TA | 13 | a0001c0001t0001g0166a0001c0001t0001g0265a0001c0001t0002g0238others(10): Show | 13 | HG00597.hp1 HG00738.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.154+6166dupT | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623164 | ||||||
chr1:2623275
|
G | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+6056C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623275 | ||||||
chr1:2623314
|
A | C | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.154+6017T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623314 | ||||||
chr1:2623506
|
C | T | 1 | a0002c0002t0003g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.154+5825G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623506 | ||||||
chr1:2623690
|
C | T | 11 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(8): Show | 17 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.154+5641G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623690 | ||||||
chr1:2623810
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.154+5521G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623810 | ||||||
chr1:2623859
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.154+5472G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623859 | ||||||
chr1:2623875
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.154+5456T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2623875 | ||||||
chr1:2624025
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154+5306C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624025 | ||||||
chr1:2624158
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.154+5173G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624158 | ||||||
chr1:2624201
|
T | A | 125 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(122): Show | 161 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.154+5130A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624201 | ||||||
chr1:2624278
|
G | A | 1 | a0011c0020t0001g0266 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154+5053C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624278 | ||||||
chr1:2624337
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG00735.hp1 HG01361.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.154+4994G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624337 | ||||||
chr1:2624371
|
A | G | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+4960T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624371 | ||||||
chr1:2624381
|
C | T | 1 | a0002c0017t0001g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.154+4950G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624381 | ||||||
chr1:2624572
|
T | C | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+4759A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624572 | ||||||
chr1:2624686
|
C | T | 113 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(110): Show | 148 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.154+4645G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624686 | ||||||
chr1:2624847
|
C | T | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+4484G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624847 | ||||||
chr1:2624907
|
C | T | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+4424G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624907 | ||||||
chr1:2624948
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.154+4383C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2624948 | ||||||
chr1:2625090
|
A | G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+4241T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625090 | ||||||
chr1:2625109
|
C | T | 116 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(113): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.154+4222G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625109 | ||||||
chr1:2625268
|
G | C | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.154+4063C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625268 | ||||||
chr1:2625270
|
G | A | 116 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(113): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.154+4061C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625270 | ||||||
chr1:2625318
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+4013G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625318 | ||||||
chr1:2625327
|
G | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+4004C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625327 | ||||||
chr1:2625328
|
A | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+4003T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625328 | ||||||
chr1:2625469
|
C | T | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+3862G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625469 | ||||||
chr1:2625548
|
G | A | 2 | a0001c0001t0002g0243a0007c0026t0002g0244 | 2 | HG00099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.154+3783C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625548 | ||||||
chr1:2625752
|
C | T | 164 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(161): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.154+3579G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625752 | ||||||
chr1:2625837
|
T | C | 1 | a0001c0001t0002g0014 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.154+3494A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625837 | ||||||
chr1:2625872
|
C | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+3459G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625872 | ||||||
chr1:2625937
|
G | GGAA | 148 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(145): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.154+3391_154+3393d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2625937 | ||||||
chr1:2626092
|
C | T | 164 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(161): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.154+3239G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626092 | ||||||
chr1:2626215
|
T | C | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154+3116A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626215 | ||||||
chr1:2626217
|
G | A | 1 | a0001c0001t0002g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.154+3114C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626217 | ||||||
chr1:2626608
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.154+2723G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626608 | ||||||
chr1:2626770
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+2561G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626770 | ||||||
chr1:2626771
|
G | A | 2 | a0002c0002t0001g0010a0008c0011t0001g0128 | 4 | HG01109.hp2 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+2560C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626771 | ||||||
chr1:2626869
|
A | C | 164 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(161): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.154+2462T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2626869 | ||||||
chr1:2627178
|
G | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.154+2153C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627178 | ||||||
chr1:2627179
|
T | TTC | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.154+2151_154+2152i others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627179 | ||||||
chr1:2627180
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02109.hp2 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.154+2151C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627180 | ||||||
chr1:2627255
|
C | T | 2 | a0002c0012t0001g0126a0006c0009t0004g0277 | 2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.154+2076G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627255 | ||||||
chr1:2627256
|
G | A | 1 | a0002c0003t0001g0280 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.154+2075C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627256 | ||||||
chr1:2627257
|
C | A | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154+2074G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627257 | ||||||
chr1:2627301
|
C | T | 165 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(162): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.154+2030G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627301 | ||||||
chr1:2627444
|
T | C | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+1887A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627444 | ||||||
chr1:2627747
|
A | G | 2 | a0002c0002t0001g0051a0002c0002t0001g0052 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.154+1584T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627747 | ||||||
chr1:2627834
|
C | A | 1 | a0002c0004t0001g0275 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.154+1497G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627834 | ||||||
chr1:2627984
|
G | A | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1347C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2627984 | ||||||
chr1:2628064
|
G | A | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.154+1267C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628064 | ||||||
chr1:2628150
|
T | G | 165 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(162): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.154+1181A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628150 | ||||||
chr1:2628167
|
C | T | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1164G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628167 | ||||||
chr1:2628191
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.154+1140C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628191 | ||||||
chr1:2628295
|
G | T | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.154+1036C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628295 | ||||||
chr1:2628299
|
C | A | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.154+1032G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628299 | ||||||
chr1:2628459
|
T | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG01168.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.154+872A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628459 | ||||||
chr1:2628461
|
C | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+870G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628461 | ||||||
chr1:2628548
|
G | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+783C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628548 | ||||||
chr1:2628659
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.154+672C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628659 | ||||||
chr1:2628679
|
TGGGGGCG others(23): Show |
T | 2 | a0002c0008t0001g0049a0002c0008t0001g0050 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154+622_154+651del others(30): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628679 | ||||||
chr1:2628915
|
C | A | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+416G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628915 | ||||||
chr1:2628957
|
G | A | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.154+374C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2628957 | ||||||
chr1:2629028
|
CGGCGGAG others(5): Show |
C | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+291_154+302del others(12): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2629028 | ||||||
chr1:2629176
|
C | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154+155G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2629176 | ||||||
chr1:2629296
|
A | G | 166 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(163): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.154+35T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 2/23 | chr1 | 2629296 | ||||||
chr1:2629536
|
C | CAGGGGAG | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-37-22_-37-16dupCT others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629536 | ||||||
chr1:2629580
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-37-59C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629580 | ||||||
chr1:2629820
|
GCCC | G | 165 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(162): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-37-302_-37-300del others(3): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629820 | ||||||
chr1:2629828
|
C | A | 3 | a0002c0002t0003g0006a0002c0002t0003g0038a0010c0015t0003g0039 | 5 | HG00642.hp1 HG01346.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-307G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629828 | ||||||
chr1:2629828
|
C | G | 1 | a0002c0002t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-37-307G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629828 | ||||||
chr1:2629829
|
C | A | 1 | a0002c0002t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-37-308G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629829 | ||||||
chr1:2629847
|
T | G | 165 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(162): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-37-326A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629847 | ||||||
chr1:2629938
|
G | A | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-417C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2629938 | ||||||
chr1:2630051
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-37-530C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630051 | ||||||
chr1:2630125
|
C | A | 1 | a0001c0001t0001g0135 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-37-604G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630125 | ||||||
chr1:2630136
|
T | A | 5 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-615A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630136 | ||||||
chr1:2630313
|
TGA | T | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-794_-37-793del others(2): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630313 | ||||||
chr1:2630408
|
G | T | 7 | a0002c0002t0001g0005a0002c0002t0001g0041a0002c0002t0001g0043others(4): Show | 10 | HG01099.hp1 HG01261.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-37-887C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630408 | ||||||
chr1:2630449
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0005g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37-942_-37-929del others(14): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630449 | ||||||
chr1:2630455
|
T | C | 1 | a0002c0012t0001g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-37-934A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630455 | ||||||
chr1:2630477
|
TGTGTGTG others(3): Show |
T | 7 | a0002c0004t0001g0267a0002c0004t0001g0268a0002c0004t0001g0269others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-966_-37-957del others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630477 | ||||||
chr1:2630516
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-37-995C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630516 | ||||||
chr1:2630541
|
GTC | G | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1022_-37-1021d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630541 | ||||||
chr1:2630546
|
C | T | 1 | a0002c0003t0001g0023 | 2 | NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-37-1025G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630546 | ||||||
chr1:2630570
|
TGTGA | T | 9 | a0001c0001t0001g0139a0001c0001t0001g0173a0001c0001t0001g0174others(6): Show | 9 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-1053_-37-1050d others(6): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630570 | ||||||
chr1:2630586
|
CGT | C | 92 | a0001c0001t0001g0025a0001c0001t0001g0130a0001c0001t0001g0137others(89): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-37-1067_-37-1066d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630586 | ||||||
chr1:2630587
|
G | C | 1 | a0002c0002t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-37-1066C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630587 | ||||||
chr1:2630638
|
C | T | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-37-1117G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630638 | ||||||
chr1:2630696
|
CGTG | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1178_-37-1176d others(5): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630696 | ||||||
chr1:2630730
|
C | T | 151 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(148): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-37-1209G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630730 | ||||||
chr1:2630746
|
CAT | C | 2 | a0002c0002t0001g0010a0008c0011t0001g0128 | 4 | HG01109.hp2 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-1227_-37-1226d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630746 | ||||||
chr1:2630777
|
CGT | C | 17 | a0001c0001t0001g0027a0001c0001t0001g0251a0001c0001t0001g0252others(14): Show | 19 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37-1258_-37-1257d others(4): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630777 | ||||||
chr1:2630835
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-37-1314G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630835 | ||||||
chr1:2630861
|
C | G | 1 | a0002c0004t0001g0275 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-37-1340G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2630861 | ||||||
chr1:2631020
|
T | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1499A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631020 | ||||||
chr1:2631328
|
T | G | 1 | a0013c0019t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-38+1538A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631328 | ||||||
chr1:2631523
|
C | T | 1 | a0006c0009t0004g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+1343G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631523 | ||||||
chr1:2631557
|
G | C | 5 | a0002c0003t0001g0013a0002c0003t0001g0028a0002c0003t0001g0278others(2): Show | 8 | HG01123.hp1 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38+1309C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631557 | ||||||
chr1:2631659
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-38+1207G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631659 | ||||||
chr1:2631663
|
C | T | 1 | a0009c0024t0002g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-38+1203G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631663 | ||||||
chr1:2631698
|
G | A | 1 | a0002c0017t0001g0129 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-38+1168C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631698 | ||||||
chr1:2631811
|
G | T | 148 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(145): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-38+1055C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631811 | ||||||
chr1:2631823
|
C | T | 2 | a0006c0009t0004g0276a0006c0009t0004g0277 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+1043G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2631823 | ||||||
chr1:2632100
|
C | T | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-38+766G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632100 | ||||||
chr1:2632197
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-38+669G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632197 | ||||||
chr1:2632398
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG02896.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+468C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632398 | ||||||
chr1:2632408
|
T | C | 1 | a0002c0004t0001g0275 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-38+458A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632408 | ||||||
chr1:2632462
|
T | C | 1 | a0002c0003t0006g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-38+404A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632462 | ||||||
chr1:2632528
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01256.hp1 HG02683.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-38+338G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632528 | ||||||
chr1:2632530
|
C | T | 1 | a0006c0009t0004g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+336G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632530 | ||||||
chr1:2632533
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+333G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632533 | ||||||
chr1:2632535
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+331G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632535 | ||||||
chr1:2632536
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+330T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632536 | ||||||
chr1:2632539
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+327G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632539 | ||||||
chr1:2632540
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+326T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632540 | ||||||
chr1:2632542
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+324T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632542 | ||||||
chr1:2632544
|
T | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+322A>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632544 | ||||||
chr1:2632545
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+321T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632545 | ||||||
chr1:2632547
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+319T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632547 | ||||||
chr1:2632550
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+316G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632550 | ||||||
chr1:2632551
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+315G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632551 | ||||||
chr1:2632557
|
A | G | 2 | a0002c0003t0001g0023a0002c0003t0006g0131 | 3 | HG00140.hp2 NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-38+309T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632557 | ||||||
chr1:2632562
|
G | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+304C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632562 | ||||||
chr1:2632564
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+302G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632564 | ||||||
chr1:2632568
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+298A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632568 | ||||||
chr1:2632573
|
G | A | 112 | a0001c0005t0001g0062a0001c0005t0001g0082a0001c0005t0001g0092others(109): Show | 145 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-38+293C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632573 | ||||||
chr1:2632575
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+291C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632575 | ||||||
chr1:2632577
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+289G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632577 | ||||||
chr1:2632580
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+286C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632580 | ||||||
chr1:2632588
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+278A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632588 | ||||||
chr1:2632591
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+275G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632591 | ||||||
chr1:2632592
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+274A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632592 | ||||||
chr1:2632601
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+265C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632601 | ||||||
chr1:2632604
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+262C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632604 | ||||||
chr1:2632605
|
G | GATTGATC others(4): Show |
1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+260_-38+261ins others(11): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632605 | ||||||
chr1:2632608
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+258G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632608 | ||||||
chr1:2632614
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+252G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632614 | ||||||
chr1:2632618
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+248G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632618 | ||||||
chr1:2632624
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+242T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632624 | ||||||
chr1:2632625
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+241G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632625 | ||||||
chr1:2632626
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+240T>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632626 | ||||||
chr1:2632633
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+233C>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632633 | ||||||
chr1:2632635
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+231G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632635 | ||||||
chr1:2632638
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+228A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632638 | ||||||
chr1:2632648
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+218A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632648 | ||||||
chr1:2632655
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+211C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632655 | ||||||
chr1:2632662
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+204T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632662 | ||||||
chr1:2632664
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+202G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632664 | ||||||
chr1:2632672
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+194A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632672 | ||||||
chr1:2632680
|
GATAAACC others(3): Show |
G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+176_-38+185del others(10): Show |
MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632680 | ||||||
chr1:2632708
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+158A>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632708 | ||||||
chr1:2632710
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+156G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632710 | ||||||
chr1:2632711
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+155G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632711 | ||||||
chr1:2632714
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+152C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632714 | ||||||
chr1:2632716
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+150G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632716 | ||||||
chr1:2632717
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+149T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632717 | ||||||
chr1:2632718
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+148G>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632718 | ||||||
chr1:2632719
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-38+147T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632719 | ||||||
chr1:2632724
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+142T>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632724 | ||||||
chr1:2632725
|
G | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+141C>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632725 | ||||||
chr1:2632726
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+140T>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632726 | ||||||
chr1:2632739
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-38+127G>C | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632739 | ||||||
chr1:2632744
|
T | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0027others(160): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-38+122A>G | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632744 | ||||||
chr1:2632751
|
C | T | 1 | a0001c0001t0002g0014 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.-38+115G>A | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632751 | ||||||
chr1:2632840
|
G | A | 1 | a0004c0007t0001g0029 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-38+26C>T | MMEL1 | ENSG00000142606.16 | transcript | ENST00000378412.8 | protein_coding | 1/23 | chr1 | 2632840 |