geneid | 157777 |
---|---|
ensemblid | ENSG00000178460.18 |
hgncid | 26368 |
symbol | MCMDC2 |
name | minichromosome maintenance domain containing 2 |
refseq_nuc | NM_173518.5 |
refseq_prot | NP_775789.3 |
ensembl_nuc | ENST00000422365.7 |
ensembl_prot | ENSP00000413632.2 |
mane_status | MANE Select |
chr | chr8 |
start | 66870771 |
end | 66922048 |
strand | + |
ver | v1.2 |
region | chr8:66870771-66922048 |
region5000 | chr8:66865771-66927048 |
regionname0 | MCMDC2_chr8_66870771_66922048 |
regionname5000 | MCMDC2_chr8_66865771_66927048 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 681 | 148 | 44 | 30 | 46 | 7 | 19 | 35 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0002 | 0/0 | 681 | 12 | 2 | 5 | 1 | 0 | 4 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0003 | 0/0 | 681 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0004 | 0/0 | 681 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0005 | 0/0 | 681 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0006 | 0/0 | 681 | 7 | 0 | 4 | 0 | 3 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0007 | 0/0 | 681 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0008 | 0/0 | 681 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0009 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0010 | 0/0 | 681 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0011 | 0/0 | 681 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0012 | 0/0 | 681 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0013 | 0/0 | 681 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2046 | 147 | 44 | 30 | 46 | 7 | 18 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0002 | 0/0 | 2046 | 10 | 0 | 5 | 1 | 0 | 4 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0003 | 0/0 | 2046 | 10 | 10 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0004 | 0/0 | 2046 | 9 | 7 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0005 | 0/0 | 2046 | 7 | 6 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0006 | 0/0 | 2046 | 7 | 0 | 4 | 0 | 3 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0007 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0008 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0009 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0010 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0011 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0012 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0013 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0014 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
c0015 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3029 | 120 | 24 | 37 | 34 | 10 | 13 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0002 | 0/0 | 3029 | 38 | 22 | 5 | 1 | 0 | 10 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0003 | 0/0 | 3029 | 9 | 7 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0004 | 0/0 | 3029 | 8 | 8 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0005 | 0/0 | 3029 | 8 | 0 | 0 | 8 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0006 | 0/0 | 3029 | 5 | 5 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0007 | 0/0 | 3029 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0008 | 0/0 | 3029 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0009 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0010 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0011 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0012 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0013 | 0/0 | 3029 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0014 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0015 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0016 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0017 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
t0018 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2046 | 147 | 44 | 30 | 46 | 7 | 18 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0015 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0002c0002 | 0/0 | 2046 | 10 | 0 | 5 | 1 | 0 | 4 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0002c0009 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0003c0003 | 0/0 | 2046 | 10 | 10 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0004c0004 | 0/0 | 2046 | 9 | 7 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0005c0005 | 0/0 | 2046 | 7 | 6 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0006c0006 | 0/0 | 2046 | 7 | 0 | 4 | 0 | 3 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0007c0007 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0008c0008 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0009c0011 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0010c0013 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0011c0012 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0012c0014 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0013c0010 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5074 | 99 | 16 | 30 | 33 | 7 | 11 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0002 | 0/0 | 5074 | 23 | 16 | 0 | 1 | 0 | 6 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0005 | 0/0 | 5074 | 8 | 0 | 0 | 8 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0006 | 0/0 | 5074 | 5 | 5 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0007 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0008 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0009 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0011 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0012 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0013 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0014 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0015 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0016 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0001t0017 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0001c0015t0001 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0002c0002t0002 | 0/0 | 5074 | 9 | 0 | 5 | 0 | 0 | 4 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0002c0002t0018 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0002c0009t0002 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0003c0003t0002 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0003c0003t0004 | 0/0 | 5074 | 8 | 8 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0004c0004t0003 | 0/0 | 5074 | 9 | 7 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0005c0005t0001 | 0/0 | 5074 | 7 | 6 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0006c0006t0001 | 0/0 | 5074 | 7 | 0 | 4 | 0 | 3 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0007c0007t0001 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0008c0008t0002 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0009c0011t0010 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0010c0013t0001 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0011c0012t0001 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0012c0014t0001 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
a0013c0010t0001 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | copy fasta | chr8 | 66865771 | 66927048 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0013g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0016g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0001t0017g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0001c0015t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0002t0018g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0009t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0002c0009t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0003c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0004c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0005c0005t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0006c0006t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0006c0006t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0006c0006t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0006c0006t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0006c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0006c0006t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0007c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0007c0007t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0008c0008t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0008c0008t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0009c0011t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0010c0013t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0011c0012t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0012c0014t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
a0013c0010t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0006 | c0006 | t0001 | g0015 | EUR | GBR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00733 | hp1 | a0006 | c0006 | t0001 | g0127 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0171 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01070 | hp1 | a0004 | c0004 | t0003 | g0005 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01071 | hp2 | a0004 | c0004 | t0003 | g0005 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01081 | hp2 | a0006 | c0006 | t0001 | g0126 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0172 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01192 | hp2 | a0006 | c0006 | t0001 | g0129 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01243 | hp1 | a0005 | c0005 | t0001 | g0161 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01255 | hp1 | a0006 | c0006 | t0001 | g0125 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01346 | hp1 | a0013 | c0010 | t0001 | g0086 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01346 | hp2 | a0012 | c0014 | t0001 | g0092 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01516 | hp2 | a0006 | c0006 | t0001 | g0015 | EUR | IBS | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01891 | hp2 | a0005 | c0005 | t0001 | g0160 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0173 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0163 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02055 | hp2 | a0008 | c0008 | t0002 | g0155 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02056 | hp2 | a0002 | c0002 | t0018 | g0168 | EAS | KHV | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02145 | hp2 | a0005 | c0005 | t0001 | g0159 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | PEL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02615 | hp1 | a0003 | c0003 | t0004 | g0106 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0114 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02647 | hp1 | a0004 | c0004 | t0003 | g0040 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0165 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02717 | hp2 | a0004 | c0004 | t0003 | g0035 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0166 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02818 | hp1 | a0004 | c0004 | t0003 | g0036 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02896 | hp1 | a0003 | c0003 | t0004 | g0148 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02922 | hp2 | a0004 | c0004 | t0003 | g0039 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02965 | hp1 | a0005 | c0005 | t0001 | g0042 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02965 | hp2 | a0003 | c0003 | t0004 | g0142 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02976 | hp1 | a0009 | c0011 | t0010 | g0056 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0169 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03041 | hp1 | a0004 | c0004 | t0003 | g0041 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0158 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0178 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03130 | hp2 | a0008 | c0008 | t0002 | g0032 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03139 | hp1 | a0005 | c0005 | t0001 | g0043 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0110 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03225 | hp2 | a0005 | c0005 | t0001 | g0061 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03453 | hp1 | a0001 | c0001 | t0017 | g0157 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03453 | hp2 | a0003 | c0003 | t0004 | g0111 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03490 | hp1 | a0001 | c0015 | t0001 | g0055 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03516 | hp1 | a0002 | c0009 | t0002 | g0162 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03516 | hp2 | a0003 | c0003 | t0002 | g0001 | AFR | ESN | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03579 | hp1 | a0003 | c0003 | t0002 | g0001 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03654 | hp1 | a0010 | c0013 | t0001 | g0011 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03688 | hp1 | a0001 | c0001 | t0013 | g0013 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0170 | SAS | BEB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18522 | hp1 | a0004 | c0004 | t0003 | g0038 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18906 | hp2 | a0005 | c0005 | t0001 | g0060 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18946 | hp1 | a0011 | c0012 | t0001 | g0147 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18946 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18994 | hp1 | a0001 | c0001 | t0016 | g0027 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18994 | hp2 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19012 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19012 | hp2 | a0001 | c0001 | t0012 | g0117 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA19240 | hp2 | a0007 | c0007 | t0001 | g0017 | AFR | YRI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ASW | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20129 | hp2 | a0007 | c0007 | t0001 | g0018 | AFR | ASW | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20752 | hp1 | a0006 | c0006 | t0001 | g0128 | EUR | TSI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | GIH | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02109 | hp2 | a0003 | c0003 | t0004 | g0141 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02486 | hp2 | a0003 | c0003 | t0004 | g0109 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02559 | hp1 | a0002 | c0009 | t0002 | g0164 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG02559 | hp2 | a0004 | c0004 | t0003 | g0037 | AFR | ACB | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | USA | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0130 | REF | REF | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0074 | REF | REF | MCMDC2_chr8_66865771_66927048 | MCMDC2 | chr8 | 66865771 | 66927048 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66874350
|
A | G | 1 | a0003 | 10 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
missense_variant | MODERATE | c.119A>G | p.Tyr40Cys | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 3/15 | 268/5074 | 119/2046 | 40/681 | chr8 | 66874350 | ||
chr8:66874398
|
C | T | 1 | a0006 | 7 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
missense_variant | MODERATE | c.167C>T | p.Ala56Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 3/15 | 316/5074 | 167/2046 | 56/681 | chr8 | 66874398 | ||
chr8:66874582
|
C | T | 1 | a0002 | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
missense_variant | MODERATE | c.281C>T | p.Thr94Met | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/15 | 430/5074 | 281/2046 | 94/681 | chr8 | 66874582 | ||
chr8:66877355
|
A | G | 1 | a0008 | 2 | HG02055.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.292A>G | p.Ile98Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 441/5074 | 292/2046 | 98/681 | chr8 | 66877355 | ||
chr8:66877444
|
T | G | 1 | a0013 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.381T>G | p.Phe127Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 530/5074 | 381/2046 | 127/681 | chr8 | 66877444 | ||
chr8:66877473
|
T | A | 1 | a0005 | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
missense_variant | MODERATE | c.410T>A | p.Met137Lys | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 559/5074 | 410/2046 | 137/681 | chr8 | 66877473 | ||
chr8:66883885
|
C | G | 1 | a0012 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.964C>G | p.Leu322Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/15 | 1113/5074 | 964/2046 | 322/681 | chr8 | 66883885 | ||
chr8:66883928
|
G | A | 1 | a0009 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1007G>A | p.Arg336His | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/15 | 1156/5074 | 1007/2046 | 336/681 | chr8 | 66883928 | ||
chr8:66890906
|
G | T | 1 | a0010 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1115G>T | p.Arg372Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/15 | 1264/5074 | 1115/2046 | 372/681 | chr8 | 66890906 | ||
chr8:66896859
|
C | T | 1 | a0011 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1526C>T | p.Pro509Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/15 | 1675/5074 | 1526/2046 | 509/681 | chr8 | 66896859 | ||
chr8:66896903
|
C | T | 1 | a0004 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
missense_variant | MODERATE | c.1570C>T | p.Pro524Ser | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/15 | 1719/5074 | 1570/2046 | 524/681 | chr8 | 66896903 | ||
chr8:66896925
|
C | G | 1 | a0007 | 2 | NA19240.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1592C>G | p.Ala531Gly | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/15 | 1741/5074 | 1592/2046 | 531/681 | chr8 | 66896925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66877471
|
A | C | 1 | a0001c0015 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.408A>C | p.Ala136Ala | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/15 | 557/5074 | 408/2046 | 136/681 | chr8 | 66877471 | ||
chr8:66890892
|
C | A | 1 | a0009c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1101C>A | p.Val367Val | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/15 | 1250/5074 | 1101/2046 | 367/681 | chr8 | 66890892 | ||
chr8:66901247
|
G | A | 1 | a0002c0002 | 10 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
synonymous_variant | LOW | c.1668G>A | p.Leu556Leu | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/15 | 1817/5074 | 1668/2046 | 556/681 | chr8 | 66901247 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66870828
|
C | T | 1 | a0001c0001t0008 | 2 | HG02486.hp1 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-92C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/15 | 3313 | chr8 | 66870828 | |||||
chr8:66874117
|
A | G | 1 | a0002c0002t0018 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 2/15 | 24 | chr8 | 66874117 | |||||
chr8:66919368
|
A | C | 2 | a0001c0001t0007a0001c0001t0017 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 199 | chr8 | 66919368 | |||||
chr8:66919632
|
T | A | 1 | a0001c0001t0009 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 463 | chr8 | 66919632 | |||||
chr8:66920152
|
G | A | 1 | a0009c0011t0010 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 983 | chr8 | 66920152 | |||||
chr8:66920281
|
T | C | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1112T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1112 | chr8 | 66920281 | |||||
chr8:66920386
|
A | G | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1217A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1217 | chr8 | 66920386 | |||||
chr8:66920423
|
G | A | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1254G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1254 | chr8 | 66920423 | |||||
chr8:66920473
|
A | G | 15 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(12): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1304A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1304 | chr8 | 66920473 | |||||
chr8:66920518
|
G | A | 1 | a0001c0001t0006 | 5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1349 | chr8 | 66920518 | |||||
chr8:66920572
|
C | T | 1 | a0001c0001t0013 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 1403 | chr8 | 66920572 | |||||
chr8:66921263
|
C | G | 1 | a0001c0001t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2094C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2094 | chr8 | 66921263 | |||||
chr8:66921268
|
C | T | 1 | a0001c0001t0016 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2099 | chr8 | 66921268 | |||||
chr8:66921346
|
C | A | 3 | a0001c0001t0005a0001c0001t0014a0001c0001t0016 | 10 | NA18946.hp2 NA18952.hp2 NA18957.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2177C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2177 | chr8 | 66921346 | |||||
chr8:66921515
|
C | A | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2346C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2346 | chr8 | 66921515 | |||||
chr8:66921574
|
T | C | 1 | a0003c0003t0004 | 8 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2405T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2405 | chr8 | 66921574 | |||||
chr8:66921696
|
G | A | 1 | a0001c0001t0014 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2527G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2527 | chr8 | 66921696 | |||||
chr8:66921935
|
T | A | 1 | a0004c0004t0003 | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2766T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2766 | chr8 | 66921935 | |||||
chr8:66921936
|
G | A | 1 | a0001c0001t0011 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2767G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2767 | chr8 | 66921936 | |||||
chr8:66921983
|
A | G | 1 | a0001c0001t0012 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2814A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2814 | chr8 | 66921983 | |||||
chr8:66922038
|
C | G | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(7): Show | 50 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2869C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 15/15 | 2869 | chr8 | 66922038 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66870864
|
A | G | 9 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89+33A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66870864 | ||||||
chr8:66871057
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-89+226G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871057 | ||||||
chr8:66871108
|
C | G | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-89+277C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871108 | ||||||
chr8:66871120
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-89+289A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871120 | ||||||
chr8:66871401
|
A | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG00733.hp2 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-89+570A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871401 | ||||||
chr8:66871478
|
C | T | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.-89+647C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871478 | ||||||
chr8:66871519
|
G | A | 2 | a0007c0007t0001g0017a0007c0007t0001g0018 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-89+688G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871519 | ||||||
chr8:66871610
|
A | G | 3 | a0005c0005t0001g0159a0005c0005t0001g0160a0005c0005t0001g0161 | 3 | HG01243.hp1 HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-89+779A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871610 | ||||||
chr8:66871640
|
G | T | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-89+809G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871640 | ||||||
chr8:66871729
|
A | G | 4 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+898A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66871729 | ||||||
chr8:66871900
|
C | CA | 48 | a0001c0001t0001g0044a0001c0001t0001g0179a0001c0001t0002g0003others(45): Show | 52 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-89+1083dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66871900 | |||||
chr8:66871900
|
C | CAA | 15 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(12): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-89+1082_-89+1083d others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66871900 | |||||
chr8:66872587
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-88-1466C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872587 | ||||||
chr8:66872590
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.-88-1463T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872590 | ||||||
chr8:66872606
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-88-1447G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872606 | ||||||
chr8:66872774
|
A | G | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-88-1279A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872774 | ||||||
chr8:66872787
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-88-1266G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872787 | ||||||
chr8:66872894
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88-1159C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872894 | ||||||
chr8:66872957
|
C | CA | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 11 | HG01261.hp2 HG01515.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-88-1074dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | |||||
chr8:66872957
|
C | CAA | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88-1075_-88-1074d others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | |||||
chr8:66872957
|
CA | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0176others(2): Show | 5 | HG01074.hp2 HG01515.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-88-1074delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | |||||
chr8:66872957
|
CAAAAAAA others(6): Show |
C | 1 | a0004c0004t0003g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-88-1086_-88-1074d others(15): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 66872957 | |||||
chr8:66872977
|
A | C | 2 | a0001c0001t0001g0150a0001c0001t0007g0158 | 2 | HG00639.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-88-1076A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872977 | ||||||
chr8:66872980
|
C | A | 1 | a0002c0009t0002g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-88-1073C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66872980 | ||||||
chr8:66873340
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-88-713G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873340 | ||||||
chr8:66873467
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-88-586A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873467 | ||||||
chr8:66873559
|
C | T | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.-88-494C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873559 | ||||||
chr8:66873628
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88-425C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873628 | ||||||
chr8:66873722
|
C | G | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-88-331C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 1/14 | chr8 | 66873722 | ||||||
chr8:66874249
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.94+15G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 2/14 | chr8 | 66874249 | ||||||
chr8:66874662
|
A | C | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+76A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66874662 | ||||||
chr8:66874851
|
C | T | 22 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(19): Show | 24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.285+265C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66874851 | ||||||
chr8:66875199
|
T | C | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.285+613T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875199 | ||||||
chr8:66875277
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.285+691T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875277 | ||||||
chr8:66875383
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.285+797A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875383 | ||||||
chr8:66875617
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.285+1031T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875617 | ||||||
chr8:66875646
|
T | C | 1 | a0001c0015t0001g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.285+1060T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875646 | ||||||
chr8:66875653
|
A | G | 1 | a0001c0001t0007g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285+1067A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875653 | ||||||
chr8:66875798
|
C | A | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.285+1212C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875798 | ||||||
chr8:66875995
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG01243.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.286-1354G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66875995 | ||||||
chr8:66876002
|
A | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.286-1347A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876002 | ||||||
chr8:66876003
|
T | C | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.286-1346T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876003 | ||||||
chr8:66876124
|
C | T | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.286-1225C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876124 | ||||||
chr8:66876399
|
G | A | 9 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-950G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876399 | ||||||
chr8:66876512
|
G | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.286-837G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876512 | ||||||
chr8:66876518
|
T | G | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.286-831T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876518 | ||||||
chr8:66876523
|
G | A | 1 | a0008c0008t0002g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.286-826G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876523 | ||||||
chr8:66876534
|
T | C | 2 | a0005c0005t0001g0060a0005c0005t0001g0061 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.286-815T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876534 | ||||||
chr8:66876712
|
A | G | 2 | a0004c0004t0003g0005a0004c0004t0003g0040 | 3 | HG01070.hp1 HG01071.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.286-637A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876712 | ||||||
chr8:66876757
|
ATGGAGTC others(18): Show |
A | 10 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(7): Show | 10 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-575_286-551del others(25): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr8 | 66876757 | |||||
chr8:66876799
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.286-550T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876799 | ||||||
chr8:66876828
|
T | G | 13 | a0001c0001t0015g0178a0002c0002t0002g0163a0002c0002t0002g0165others(10): Show | 13 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.286-521T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876828 | ||||||
chr8:66876877
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-472T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876877 | ||||||
chr8:66876885
|
C | T | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286-464C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876885 | ||||||
chr8:66876981
|
C | T | 5 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-368C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66876981 | ||||||
chr8:66877007
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.286-342G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66877007 | ||||||
chr8:66877054
|
C | T | 9 | a0002c0002t0002g0163a0002c0002t0002g0166a0002c0002t0002g0167others(6): Show | 9 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-295C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66877054 | ||||||
chr8:66877055
|
G | A | 1 | a0004c0004t0003g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.286-294G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 4/14 | chr8 | 66877055 | ||||||
chr8:66877627
|
A | C | 9 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+83A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66877627 | ||||||
chr8:66877863
|
T | TA | 5 | a0001c0001t0002g0020a0001c0001t0002g0021a0003c0003t0002g0001others(2): Show | 6 | HG02258.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+340dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 66877863 | |||||
chr8:66877863
|
T | TAA | 7 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0180others(4): Show | 7 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+339_481+340dup others(2): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 66877863 | |||||
chr8:66877863
|
TA | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0143a0001c0001t0001g0145others(2): Show | 5 | HG01516.hp1 HG02897.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+340delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 66877863 | |||||
chr8:66877886
|
T | C | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+342T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66877886 | ||||||
chr8:66878012
|
G | T | 5 | a0004c0004t0003g0036a0004c0004t0003g0037a0004c0004t0003g0038others(2): Show | 5 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+468G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878012 | ||||||
chr8:66878035
|
C | T | 3 | a0003c0003t0004g0141a0003c0003t0004g0142a0008c0008t0002g0032 | 3 | HG02109.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.481+491C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878035 | ||||||
chr8:66878102
|
C | T | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482-472C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878102 | ||||||
chr8:66878392
|
A | C | 9 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0167others(6): Show | 9 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-182A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878392 | ||||||
chr8:66878407
|
G | A | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.482-167G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878407 | ||||||
chr8:66878415
|
T | A | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482-159T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 5/14 | chr8 | 66878415 | ||||||
chr8:66878928
|
A | G | 2 | a0005c0005t0001g0060a0005c0005t0001g0061 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.709+9A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66878928 | ||||||
chr8:66879007
|
A | G | 2 | a0001c0001t0002g0185a0001c0001t0002g0186 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.709+88A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879007 | ||||||
chr8:66879008
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.709+89C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879008 | ||||||
chr8:66879284
|
T | C | 35 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(32): Show | 37 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.709+365T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879284 | ||||||
chr8:66879486
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.709+567G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879486 | ||||||
chr8:66879543
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.709+624A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879543 | ||||||
chr8:66879619
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.709+700G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879619 | ||||||
chr8:66879663
|
T | G | 1 | a0001c0001t0011g0064 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.709+744T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879663 | ||||||
chr8:66879762
|
A | G | 22 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(19): Show | 24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.709+843A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66879762 | ||||||
chr8:66880318
|
C | G | 1 | a0001c0001t0002g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.710-531C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880318 | ||||||
chr8:66880472
|
T | C | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.710-377T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880472 | ||||||
chr8:66880684
|
A | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.710-165A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880684 | ||||||
chr8:66880821
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.710-28T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 7/14 | chr8 | 66880821 | ||||||
chr8:66881006
|
A | G | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+32A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881006 | ||||||
chr8:66881243
|
A | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+269A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881243 | ||||||
chr8:66881516
|
A | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+542A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881516 | ||||||
chr8:66881636
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.835+662A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881636 | ||||||
chr8:66881690
|
G | T | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.835+716G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881690 | ||||||
chr8:66881834
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.835+860A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66881834 | ||||||
chr8:66882431
|
T | G | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.836-1326T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882431 | ||||||
chr8:66882547
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.836-1210A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882547 | ||||||
chr8:66882589
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.836-1168C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882589 | ||||||
chr8:66882865
|
G | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-892G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882865 | ||||||
chr8:66882976
|
C | A | 5 | a0001c0001t0001g0066a0001c0001t0006g0007a0001c0001t0006g0065others(2): Show | 6 | HG01891.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.836-781C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66882976 | ||||||
chr8:66883170
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.836-587A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883170 | ||||||
chr8:66883262
|
T | G | 35 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(32): Show | 37 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.836-495T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883262 | ||||||
chr8:66883309
|
C | G | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.836-448C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883309 | ||||||
chr8:66883567
|
G | A | 2 | a0001c0001t0006g0007a0001c0001t0006g0065 | 3 | HG01891.hp1 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.836-190G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 8/14 | chr8 | 66883567 | ||||||
chr8:66884253
|
CT | C | 9 | a0001c0001t0001g0066a0004c0004t0003g0005a0004c0004t0003g0035others(6): Show | 10 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1073+260delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884253 | ||||||
chr8:66884306
|
C | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1073+312C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884306 | ||||||
chr8:66884324
|
C | A | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1073+330C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884324 | ||||||
chr8:66884416
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG01070.hp2 HG01255.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+422G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884416 | ||||||
chr8:66884738
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1073+744A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884738 | ||||||
chr8:66884743
|
C | G | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1073+749C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884743 | ||||||
chr8:66884884
|
CTCCA | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1073+891_1073+894d others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66884884 | ||||||
chr8:66885027
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1073+1033T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885027 | ||||||
chr8:66885071
|
A | G | 189 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1073+1077A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885071 | ||||||
chr8:66885161
|
G | A | 14 | a0001c0001t0001g0075a0001c0001t0002g0016a0001c0001t0002g0019others(11): Show | 15 | HG01081.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1073+1167G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885161 | ||||||
chr8:66885167
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1073+1173A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885167 | ||||||
chr8:66885195
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1073+1201T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885195 | ||||||
chr8:66885204
|
G | T | 4 | a0001c0001t0006g0007a0001c0001t0006g0065a0001c0001t0006g0067others(1): Show | 5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1210G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885204 | ||||||
chr8:66885206
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1073+1212G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885206 | ||||||
chr8:66885455
|
A | G | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1073+1461A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885455 | ||||||
chr8:66885479
|
G | A | 2 | a0002c0002t0002g0167a0002c0002t0018g0168 | 2 | HG02056.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1073+1485G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885479 | ||||||
chr8:66885611
|
TG | T | 5 | a0001c0001t0001g0066a0001c0001t0006g0007a0001c0001t0006g0065others(2): Show | 6 | HG01891.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1073+1618delG | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885611 | ||||||
chr8:66885824
|
A | G | 1 | a0001c0001t0006g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1073+1830A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885824 | ||||||
chr8:66885955
|
A | G | 1 | a0003c0003t0004g0142 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1073+1961A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66885955 | ||||||
chr8:66886046
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+2052G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886046 | ||||||
chr8:66886092
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1073+2098T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886092 | ||||||
chr8:66886121
|
A | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG01243.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1073+2127A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886121 | ||||||
chr8:66886145
|
G | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1073+2151G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886145 | ||||||
chr8:66886158
|
C | CT | 12 | a0001c0001t0001g0132a0001c0001t0002g0024a0001c0001t0002g0184others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1073+2187dupT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66886158 | |||||
chr8:66886158
|
CT | C | 15 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0079others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1073+2187delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66886158 | |||||
chr8:66886186
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1073+2192C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886186 | ||||||
chr8:66886535
|
G | T | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1073+2541G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886535 | ||||||
chr8:66886570
|
T | G | 1 | a0004c0004t0003g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1073+2576T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886570 | ||||||
chr8:66886815
|
G | A | 184 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 196 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.1073+2821G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886815 | ||||||
chr8:66886849
|
A | G | 6 | a0006c0006t0001g0015a0006c0006t0001g0125a0006c0006t0001g0126others(3): Show | 7 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+2855A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66886849 | ||||||
chr8:66887265
|
C | T | 9 | a0001c0001t0005g0002a0001c0001t0005g0004a0001c0001t0005g0023others(6): Show | 10 | NA18946.hp2 NA18952.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.1073+3271C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887265 | ||||||
chr8:66887310
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1073+3316T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887310 | ||||||
chr8:66887315
|
G | A | 9 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+3321G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887315 | ||||||
chr8:66887384
|
C | CA | 6 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0087others(3): Show | 7 | HG00642.hp1 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073+3408dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66887384 | |||||
chr8:66887384
|
CA | C | 53 | a0001c0001t0001g0124a0001c0001t0002g0003a0001c0001t0002g0016others(50): Show | 57 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(54): Show |
intron_variant | MODIFIER | c.1073+3408delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66887384 | |||||
chr8:66887384
|
CAA | C | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1073+3407_1073+340 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66887384 | |||||
chr8:66887399
|
A | G | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1073+3405A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887399 | ||||||
chr8:66887547
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-3318C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887547 | ||||||
chr8:66887856
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1074-3009A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887856 | ||||||
chr8:66887873
|
CAG | C | 5 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0122others(2): Show | 5 | HG00621.hp1 HG01081.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-2991_1074-299 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887873 | ||||||
chr8:66887903
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-2962T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66887903 | ||||||
chr8:66888111
|
C | T | 18 | a0001c0001t0001g0121a0001c0001t0002g0003a0001c0001t0002g0022others(15): Show | 20 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(17): Show |
intron_variant | MODIFIER | c.1074-2754C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888111 | ||||||
chr8:66888112
|
G | A | 2 | a0002c0009t0002g0162a0002c0009t0002g0164 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1074-2753G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888112 | ||||||
chr8:66888247
|
AT | A | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1074-2611delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66888247 | |||||
chr8:66888389
|
T | C | 1 | a0001c0001t0005g0023 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1074-2476T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888389 | ||||||
chr8:66888430
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1074-2435T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888430 | ||||||
chr8:66888742
|
T | C | 13 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(10): Show | 14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074-2123T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888742 | ||||||
chr8:66888821
|
G | A | 22 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(19): Show | 24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074-2044G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66888821 | ||||||
chr8:66889075
|
G | A | 1 | a0013c0010t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1074-1790G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889075 | ||||||
chr8:66889379
|
C | T | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1074-1486C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889379 | ||||||
chr8:66889472
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0120 | 3 | HG00544.hp2 NA19011.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1074-1393C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889472 | ||||||
chr8:66889549
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1074-1316G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889549 | ||||||
chr8:66889591
|
A | G | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1074-1274A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889591 | ||||||
chr8:66889754
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1074-1111C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889754 | ||||||
chr8:66889968
|
A | G | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1074-897A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66889968 | ||||||
chr8:66890001
|
A | AT | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-863dupT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 66890001 | |||||
chr8:66890030
|
C | G | 22 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(19): Show | 24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074-835C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890030 | ||||||
chr8:66890169
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1074-696C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890169 | ||||||
chr8:66890402
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1074-463C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890402 | ||||||
chr8:66890519
|
G | C | 13 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(10): Show | 14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074-346G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890519 | ||||||
chr8:66890555
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-310C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 9/14 | chr8 | 66890555 | ||||||
chr8:66891293
|
T | A | 187 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(184): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1279+223T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891293 | ||||||
chr8:66891434
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0149 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1279+364A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891434 | ||||||
chr8:66891504
|
G | A | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+434G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891504 | ||||||
chr8:66891518
|
T | A | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1279+448T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891518 | ||||||
chr8:66891720
|
C | T | 1 | a0001c0001t0012g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1279+650C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891720 | ||||||
chr8:66891917
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1279+847T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891917 | ||||||
chr8:66891981
|
C | T | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+911C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891981 | ||||||
chr8:66891995
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1279+925G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66891995 | ||||||
chr8:66892260
|
C | G | 22 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(19): Show | 24 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1279+1190C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892260 | ||||||
chr8:66892542
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1279+1472C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892542 | ||||||
chr8:66892581
|
G | C | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+1511G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892581 | ||||||
chr8:66892815
|
C | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279+1745C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892815 | ||||||
chr8:66892956
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1279+1886T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66892956 | ||||||
chr8:66893174
|
T | G | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279+2104T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66893174 | ||||||
chr8:66893688
|
A | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-2482A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66893688 | ||||||
chr8:66893851
|
G | A | 187 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(184): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1280-2319G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66893851 | ||||||
chr8:66893865
|
TG | T | 125 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0049others(122): Show | 133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1280-2303delG | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66893865 | |||||
chr8:66894221
|
A | G | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1280-1949A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894221 | ||||||
chr8:66894285
|
A | C | 1 | a0006c0006t0001g0015 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1280-1885A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894285 | ||||||
chr8:66894374
|
T | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-1796T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894374 | ||||||
chr8:66894405
|
A | G | 2 | a0001c0001t0002g0185a0001c0001t0002g0186 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1280-1765A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894405 | ||||||
chr8:66894665
|
G | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-1505G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894665 | ||||||
chr8:66894714
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1280-1456C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894714 | ||||||
chr8:66894830
|
A | T | 1 | a0001c0001t0006g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1280-1340A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894830 | ||||||
chr8:66894914
|
G | A | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1280-1256G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66894914 | ||||||
chr8:66895014
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1280-1156C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895014 | ||||||
chr8:66895163
|
C | T | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1280-1007C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895163 | ||||||
chr8:66895400
|
C | CT | 5 | a0006c0006t0001g0015a0006c0006t0001g0126a0006c0006t0001g0127others(2): Show | 6 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-754dupT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66895400 | |||||
chr8:66895400
|
C | CTT | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-755_1280-754d others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66895400 | |||||
chr8:66895400
|
CT | C | 9 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0001g0119others(6): Show | 10 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1280-754delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 66895400 | |||||
chr8:66895462
|
A | G | 1 | a0005c0005t0001g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1280-708A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895462 | ||||||
chr8:66895944
|
G | A | 43 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(40): Show | 46 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1280-226G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 10/14 | chr8 | 66895944 | ||||||
chr8:66896573
|
T | A | 9 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447-207T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 11/14 | chr8 | 66896573 | ||||||
chr8:66896620
|
A | T | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1447-160A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 11/14 | chr8 | 66896620 | ||||||
chr8:66896774
|
A | G | 1 | a0003c0003t0004g0114 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.1447-6A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 11/14 | chr8 | 66896774 | ||||||
chr8:66897413
|
AAAAAAAA others(1): Show |
A | 10 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(7): Show | 10 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1626+469_1626+476d others(10): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66897413 | |||||
chr8:66897728
|
C | A | 6 | a0006c0006t0001g0015a0006c0006t0001g0125a0006c0006t0001g0126others(3): Show | 7 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626+769C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66897728 | ||||||
chr8:66897915
|
T | C | 1 | a0004c0004t0003g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1626+956T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66897915 | ||||||
chr8:66898001
|
C | T | 6 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+1042C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898001 | ||||||
chr8:66898149
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1626+1190T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898149 | ||||||
chr8:66898166
|
C | T | 1 | a0004c0004t0003g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1626+1207C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898166 | ||||||
chr8:66898342
|
T | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1626+1383T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898342 | ||||||
chr8:66898366
|
C | T | 2 | a0007c0007t0001g0017a0007c0007t0001g0018 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1626+1407C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898366 | ||||||
chr8:66898624
|
C | CA | 6 | a0001c0001t0001g0090a0001c0001t0001g0145a0001c0001t0002g0152others(3): Show | 6 | HG01106.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+1684dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66898624 | |||||
chr8:66898624
|
CA | C | 31 | a0001c0001t0001g0072a0001c0001t0001g0083a0001c0001t0001g0113others(28): Show | 32 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(29): Show |
intron_variant | MODIFIER | c.1626+1684delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66898624 | |||||
chr8:66898737
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1626+1778G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898737 | ||||||
chr8:66898752
|
G | A | 13 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(10): Show | 14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1626+1793G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898752 | ||||||
chr8:66898868
|
A | G | 6 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+1909A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66898868 | ||||||
chr8:66899343
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1627-1863C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899343 | ||||||
chr8:66899624
|
C | T | 189 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1627-1582C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899624 | ||||||
chr8:66899644
|
C | T | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1627-1562C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899644 | ||||||
chr8:66899680
|
T | C | 1 | a0004c0004t0003g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1627-1526T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899680 | ||||||
chr8:66899710
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1627-1496A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899710 | ||||||
chr8:66899791
|
C | T | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1627-1415C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899791 | ||||||
chr8:66899892
|
C | T | 2 | a0002c0009t0002g0162a0002c0009t0002g0164 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1627-1314C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899892 | ||||||
chr8:66899920
|
G | A | 1 | a0012c0014t0001g0092 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1627-1286G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66899920 | ||||||
chr8:66899965
|
C | CA | 13 | a0001c0001t0008g0006a0002c0002t0002g0163a0002c0002t0002g0165others(10): Show | 14 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627-1232dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 66899965 | |||||
chr8:66900089
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1627-1117C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900089 | ||||||
chr8:66900163
|
G | A | 1 | a0007c0007t0001g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627-1043G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900163 | ||||||
chr8:66900164
|
C | T | 1 | a0003c0003t0002g0001 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1627-1042C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900164 | ||||||
chr8:66900298
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1627-908C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900298 | ||||||
chr8:66900308
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1627-898C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900308 | ||||||
chr8:66900335
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0088others(3): Show | 7 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-871G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900335 | ||||||
chr8:66900336
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1627-870G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900336 | ||||||
chr8:66900398
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1627-808A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900398 | ||||||
chr8:66900457
|
A | C | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1627-749A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900457 | ||||||
chr8:66900667
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1627-539C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900667 | ||||||
chr8:66900803
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1627-403G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900803 | ||||||
chr8:66900857
|
C | T | 1 | a0005c0005t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1627-349C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66900857 | ||||||
chr8:66901029
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1627-177A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66901029 | ||||||
chr8:66901086
|
C | T | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1627-120C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66901086 | ||||||
chr8:66901155
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1627-51T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 12/14 | chr8 | 66901155 | ||||||
chr8:66901398
|
A | G | 184 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 196 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.1769+50A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901398 | ||||||
chr8:66901630
|
T | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1769+282T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901630 | ||||||
chr8:66901674
|
G | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1769+326G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901674 | ||||||
chr8:66901833
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0124 | 2 | NA18957.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1769+485A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901833 | ||||||
chr8:66901944
|
A | T | 1 | a0001c0001t0002g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1769+596A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66901944 | ||||||
chr8:66902006
|
G | T | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1769+658G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902006 | ||||||
chr8:66902127
|
A | AAGAACAG others(54): Show |
1 | a0001c0001t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1769+783_1769+843d others(63): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902127 | |||||
chr8:66902408
|
G | C | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1769+1060G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902408 | ||||||
chr8:66902684
|
T | C | 1 | a0001c0001t0016g0027 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1769+1336T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902684 | ||||||
chr8:66902692
|
C | CA | 20 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0101others(17): Show | 22 | HG01346.hp2 HG01358.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+1364dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | |||||
chr8:66902692
|
C | CAA | 11 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0054others(8): Show | 12 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1769+1363_1769+136 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | |||||
chr8:66902692
|
C | CAAA | 6 | a0001c0001t0002g0016a0001c0001t0002g0181a0001c0001t0002g0184others(3): Show | 6 | HG02109.hp1 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1362_1769+136 others(7): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | |||||
chr8:66902692
|
C | CAAAA | 6 | a0001c0001t0001g0048a0001c0001t0001g0105a0001c0001t0002g0021others(3): Show | 6 | HG01981.hp1 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1361_1769+136 others(8): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | |||||
chr8:66902692
|
CAA | C | 14 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0119others(11): Show | 17 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1769+1363_1769+136 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902692 | |||||
chr8:66902705
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0017g0157 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1769+1359_1769+137 others(18): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902705 | |||||
chr8:66902707
|
AAAAAATA others(1): Show |
A | 7 | a0001c0001t0001g0120a0002c0002t0002g0163a0002c0002t0002g0165others(4): Show | 7 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1769+1361_1769+136 others(12): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902707 | |||||
chr8:66902707
|
AAAAAATA others(7): Show |
A | 2 | a0001c0001t0007g0156a0001c0001t0007g0158 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1769+1361_1769+137 others(18): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902707 | |||||
chr8:66902709
|
A | T | 13 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0121others(10): Show | 13 | HG01074.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1769+1361A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902709 | ||||||
chr8:66902711
|
A | AAAAAAAA others(16): Show |
1 | a0004c0004t0003g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(27): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AAAAAAAA others(15): Show |
1 | a0004c0004t0003g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(26): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AAAAAAAA others(16): Show |
1 | a0004c0004t0003g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(27): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AAAAAAAA others(15): Show |
1 | a0004c0004t0003g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(26): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AAAAAAAA others(12): Show |
1 | a0004c0004t0003g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(23): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AAAAAAAA others(13): Show |
1 | a0004c0004t0003g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1769+1364_1769+136 others(24): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1769+1364_1769+136 others(14): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AATATAT | 6 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0062others(3): Show | 7 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1769+1389_1769+139 others(10): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0108 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1769+1385_1769+139 others(14): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902711
|
A | T | 37 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0051others(34): Show | 40 | HG00544.hp2 HG00621.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1769+1363A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902711 | ||||||
chr8:66902711
|
AAT | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0144a0001c0001t0002g0034others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1769+1393_1769+139 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66902711 | |||||
chr8:66902712
|
AT | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG00639.hp1 HG00639.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1365delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902712 | ||||||
chr8:66902712
|
ATAT | A | 3 | a0001c0001t0002g0033a0006c0006t0001g0126a0008c0008t0002g0032 | 3 | HG01081.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1769+1365_1769+136 others(7): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902712 | ||||||
chr8:66902713
|
T | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0058others(51): Show | 58 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1769+1365T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902713 | ||||||
chr8:66902715
|
T | A | 44 | a0001c0001t0001g0009a0001c0001t0001g0081a0001c0001t0001g0082others(41): Show | 48 | HG00639.hp1 HG00735.hp2 HG01993.hp2 others(45): Show |
intron_variant | MODIFIER | c.1769+1367T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902715 | ||||||
chr8:66902717
|
T | A | 21 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0002g0016others(18): Show | 21 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1769+1369T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902717 | ||||||
chr8:66902719
|
T | A | 9 | a0001c0001t0002g0033a0001c0001t0002g0152a0001c0001t0002g0153others(6): Show | 9 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1769+1371T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902719 | ||||||
chr8:66902721
|
T | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0004c0004t0003g0035others(3): Show | 6 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769+1373T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902721 | ||||||
chr8:66902723
|
T | A | 3 | a0004c0004t0003g0035a0004c0004t0003g0038a0008c0008t0002g0032 | 3 | HG02717.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1769+1375T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902723 | ||||||
chr8:66902725
|
T | A | 1 | a0004c0004t0003g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1769+1377T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902725 | ||||||
chr8:66902739
|
T | C | 1 | a0001c0001t0005g0029 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1769+1391T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902739 | ||||||
chr8:66902741
|
T | C | 21 | a0001c0001t0001g0105a0001c0001t0002g0003a0001c0001t0002g0022others(18): Show | 23 | HG01255.hp1 HG02738.hp1 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.1769+1393T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902741 | ||||||
chr8:66902834
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1769+1486A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902834 | ||||||
chr8:66902859
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1769+1511C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66902859 | ||||||
chr8:66903120
|
C | CA | 38 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 41 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1769+1786dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66903120 | |||||
chr8:66903186
|
A | G | 1 | a0011c0012t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1769+1838A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903186 | ||||||
chr8:66903329
|
ATTTATAC others(8): Show |
A | 2 | a0001c0001t0001g0080a0001c0001t0001g0096 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1770-1894_1770-188 others(19): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66903329 | |||||
chr8:66903346
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0096 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1770-1880T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903346 | ||||||
chr8:66903501
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1770-1725G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903501 | ||||||
chr8:66903536
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1770-1690C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903536 | ||||||
chr8:66903637
|
G | C | 5 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1770-1589G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903637 | ||||||
chr8:66903845
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1770-1381G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66903845 | ||||||
chr8:66904565
|
T | TA | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1770-660dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 66904565 | |||||
chr8:66904947
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1770-279C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 13/14 | chr8 | 66904947 | ||||||
chr8:66905460
|
T | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1879+125T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905460 | ||||||
chr8:66905503
|
T | C | 1 | a0004c0004t0003g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1879+168T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905503 | ||||||
chr8:66905788
|
C | T | 1 | a0011c0012t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1879+453C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905788 | ||||||
chr8:66905847
|
G | A | 19 | a0001c0001t0001g0066a0001c0001t0006g0007a0001c0001t0006g0065others(16): Show | 21 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1879+512G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905847 | ||||||
chr8:66905918
|
T | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1879+583T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905918 | ||||||
chr8:66905927
|
A | C | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+592A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905927 | ||||||
chr8:66905973
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1879+638C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66905973 | ||||||
chr8:66906019
|
AG | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1879+685delG | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906019 | ||||||
chr8:66906020
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+685G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906020 | ||||||
chr8:66906054
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1879+719C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906054 | ||||||
chr8:66906237
|
G | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0180a0001c0001t0002g0181others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1879+902G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906237 | ||||||
chr8:66906784
|
A | T | 13 | a0001c0001t0001g0150a0001c0001t0007g0156a0001c0001t0007g0158others(10): Show | 13 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1879+1449A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906784 | ||||||
chr8:66906787
|
T | A | 1 | a0008c0008t0002g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1879+1452T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66906787 | ||||||
chr8:66907191
|
G | A | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1879+1856G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907191 | ||||||
chr8:66907313
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1879+1978G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907313 | ||||||
chr8:66907423
|
A | T | 1 | a0001c0001t0005g0045 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1879+2088A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907423 | ||||||
chr8:66907604
|
G | A | 13 | a0001c0001t0015g0178a0002c0002t0002g0163a0002c0002t0002g0165others(10): Show | 13 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1879+2269G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907604 | ||||||
chr8:66907644
|
G | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG00733.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1879+2309G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907644 | ||||||
chr8:66907869
|
CT | C | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+2542delT | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66907869 | |||||
chr8:66907978
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1879+2643C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66907978 | ||||||
chr8:66908165
|
G | A | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1879+2830G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908165 | ||||||
chr8:66908251
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+2916G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908251 | ||||||
chr8:66908380
|
C | A | 1 | a0004c0004t0003g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1879+3045C>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908380 | ||||||
chr8:66908409
|
T | A | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1879+3074T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908409 | ||||||
chr8:66908523
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+3188C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908523 | ||||||
chr8:66908551
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1879+3216G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66908551 | ||||||
chr8:66909176
|
C | T | 4 | a0001c0001t0002g0152a0001c0001t0002g0153a0008c0008t0002g0032others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879+3841C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909176 | ||||||
chr8:66909429
|
G | T | 1 | a0003c0003t0004g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1879+4094G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909429 | ||||||
chr8:66909437
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1879+4102G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909437 | ||||||
chr8:66909809
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+4474G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909809 | ||||||
chr8:66909821
|
A | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0049others(20): Show | 24 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1879+4486A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909821 | ||||||
chr8:66909961
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1879+4626G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66909961 | ||||||
chr8:66910079
|
G | A | 8 | a0003c0003t0004g0106a0003c0003t0004g0109a0003c0003t0004g0110others(5): Show | 8 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1879+4744G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910079 | ||||||
chr8:66910180
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1879+4845T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910180 | ||||||
chr8:66910240
|
T | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(58): Show | 66 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1879+4905T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910240 | ||||||
chr8:66910247
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+4912C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910247 | ||||||
chr8:66910324
|
T | A | 33 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(30): Show | 35 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.1879+4989T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910324 | ||||||
chr8:66910325
|
C | G | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1879+4990C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910325 | ||||||
chr8:66910581
|
G | C | 1 | a0001c0001t0006g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1879+5246G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910581 | ||||||
chr8:66910666
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1879+5331G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910666 | ||||||
chr8:66910867
|
C | G | 2 | a0002c0002t0002g0169a0002c0002t0002g0170 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1879+5532C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66910867 | ||||||
chr8:66911498
|
G | A | 9 | a0001c0001t0001g0133a0004c0004t0003g0005a0004c0004t0003g0035others(6): Show | 10 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1879+6163G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911498 | ||||||
chr8:66911611
|
A | ATCAGGAG others(1261): Show |
8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1879+6291_1879+629 others(1272): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66911611 | |||||
chr8:66911628
|
A | C | 1 | a0011c0012t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1879+6293A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911628 | ||||||
chr8:66911754
|
C | T | 26 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(23): Show | 27 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.1879+6419C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911754 | ||||||
chr8:66911771
|
C | T | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1879+6436C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66911771 | ||||||
chr8:66912028
|
G | A | 7 | a0005c0005t0001g0042a0005c0005t0001g0043a0005c0005t0001g0060others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1879+6693G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912028 | ||||||
chr8:66912237
|
C | T | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-6766C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912237 | ||||||
chr8:66912238
|
G | A | 3 | a0001c0001t0002g0184a0001c0001t0002g0185a0001c0001t0002g0186 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1880-6765G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912238 | ||||||
chr8:66912378
|
C | T | 14 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(11): Show | 15 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1880-6625C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912378 | ||||||
chr8:66912382
|
G | C | 1 | a0003c0003t0004g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1880-6621G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912382 | ||||||
chr8:66912458
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-6545G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912458 | ||||||
chr8:66912592
|
A | C | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG01070.hp2 HG01255.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1880-6411A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912592 | ||||||
chr8:66912898
|
G | A | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-6105G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66912898 | ||||||
chr8:66913688
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-5315G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913688 | ||||||
chr8:66913731
|
C | T | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1880-5272C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913731 | ||||||
chr8:66913833
|
G | A | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1880-5170G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913833 | ||||||
chr8:66913915
|
G | A | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1880-5088G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66913915 | ||||||
chr8:66913962
|
T | TA | 23 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0145others(20): Show | 23 | HG00099.hp2 HG00741.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1880-5018dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66913962 | |||||
chr8:66913962
|
T | TAA | 6 | a0001c0001t0008g0006a0002c0002t0002g0166a0002c0002t0002g0171others(3): Show | 7 | HG00741.hp2 HG01978.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1880-5019_1880-501 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66913962 | |||||
chr8:66913962
|
TA | T | 33 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0139others(30): Show | 36 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1880-5018delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66913962 | |||||
chr8:66914076
|
G | A | 1 | a0001c0001t0008g0006 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1880-4927G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914076 | ||||||
chr8:66914122
|
A | T | 1 | a0002c0009t0002g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1880-4881A>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914122 | ||||||
chr8:66914177
|
A | G | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1880-4826A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914177 | ||||||
chr8:66914217
|
A | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0075others(4): Show | 8 | HG00544.hp2 HG00621.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1880-4786A>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914217 | ||||||
chr8:66914283
|
C | CA | 17 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0095others(14): Show | 19 | HG00099.hp1 HG00741.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-4699dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | |||||
chr8:66914283
|
CA | C | 74 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(71): Show | 76 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.1880-4699delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | |||||
chr8:66914283
|
CAA | C | 7 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(4): Show | 8 | HG02258.hp1 HG02809.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.1880-4700_1880-469 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | |||||
chr8:66914283
|
CAAA | C | 19 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(16): Show | 21 | HG02055.hp2 HG02615.hp2 HG02738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1880-4701_1880-469 others(7): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66914283 | |||||
chr8:66914525
|
G | C | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-4478G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914525 | ||||||
chr8:66914793
|
G | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-4210G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914793 | ||||||
chr8:66914834
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1880-4169G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914834 | ||||||
chr8:66914855
|
G | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1880-4148G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914855 | ||||||
chr8:66914972
|
T | C | 96 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0049others(93): Show | 102 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.1880-4031T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66914972 | ||||||
chr8:66915162
|
T | TA | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-3833dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915162 | |||||
chr8:66915171
|
T | A | 8 | a0004c0004t0003g0005a0004c0004t0003g0035a0004c0004t0003g0036others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-3832T>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915171 | ||||||
chr8:66915329
|
G | A | 1 | a0002c0002t0018g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1880-3674G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915329 | ||||||
chr8:66915367
|
G | A | 1 | a0009c0011t0010g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1880-3636G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915367 | ||||||
chr8:66915451
|
C | CA | 12 | a0002c0002t0002g0163a0002c0002t0002g0165a0002c0002t0002g0166others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1880-3540dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915451 | |||||
chr8:66915451
|
CA | C | 17 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(14): Show | 19 | HG02738.hp1 HG03017.hp2 HG03540.hp1 others(16): Show |
intron_variant | MODIFIER | c.1880-3540delA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915451 | |||||
chr8:66915495
|
TTA | T | 48 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(45): Show | 51 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(48): Show |
intron_variant | MODIFIER | c.1880-3502_1880-350 others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915495 | |||||
chr8:66915548
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1880-3455G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915548 | ||||||
chr8:66915640
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1880-3363C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915640 | ||||||
chr8:66915641
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1880-3362G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915641 | ||||||
chr8:66915750
|
G | T | 2 | a0005c0005t0001g0060a0005c0005t0001g0061 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1880-3253G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915750 | ||||||
chr8:66915910
|
G | GA | 60 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(57): Show | 65 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.1880-3091dupA | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66915910 | |||||
chr8:66915970
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1880-3033T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66915970 | ||||||
chr8:66916161
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0102others(1): Show | 4 | HG00280.hp1 HG01071.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1880-2842G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66916161 | ||||||
chr8:66916186
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0075others(4): Show | 8 | HG00544.hp2 HG00621.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1880-2817A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66916186 | ||||||
chr8:66916545
|
C | G | 37 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0024others(34): Show | 39 | HG00741.hp2 HG01192.hp1 HG01978.hp1 others(36): Show |
intron_variant | MODIFIER | c.1880-2458C>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66916545 | ||||||
chr8:66917158
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1880-1845A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917158 | ||||||
chr8:66917194
|
T | C | 14 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(11): Show | 15 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1880-1809T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917194 | ||||||
chr8:66917290
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 5 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1880-1713C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917290 | ||||||
chr8:66917892
|
T | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0016a0001c0001t0002g0019others(58): Show | 66 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1880-1111T>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66917892 | ||||||
chr8:66918027
|
A | G | 2 | a0002c0009t0002g0162a0002c0009t0002g0164 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1880-976A>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918027 | ||||||
chr8:66918067
|
TTTTG | T | 3 | a0001c0001t0007g0156a0001c0001t0007g0158a0001c0001t0017g0157 | 3 | HG03098.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1880-932_1880-929d others(6): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66918067 | |||||
chr8:66918222
|
C | T | 3 | a0006c0006t0001g0015a0006c0006t0001g0125a0006c0006t0001g0129 | 4 | HG00099.hp1 HG01192.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1880-781C>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918222 | ||||||
chr8:66918271
|
T | TTG | 24 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0049others(21): Show | 25 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1880-731_1880-730i others(4): Show |
MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 66918271 | |||||
chr8:66918800
|
G | C | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1880-203G>C | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918800 | ||||||
chr8:66918844
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1880-159G>A | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918844 | ||||||
chr8:66918898
|
T | G | 1 | a0001c0001t0015g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1880-105T>G | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918898 | ||||||
chr8:66918971
|
G | T | 1 | a0004c0004t0003g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1880-32G>T | MCMDC2 | ENSG00000178460.18 | transcript | ENST00000422365.7 | protein_coding | 14/14 | chr8 | 66918971 |