geneid | 64087 |
---|---|
ensemblid | ENSG00000131844.17 |
hgncid | 6937 |
symbol | MCCC2 |
name | methylcrotonyl-CoA carboxylase subunit 2 |
refseq_nuc | NM_022132.5 |
refseq_prot | NP_071415.1 |
ensembl_nuc | ENST00000340941.11 |
ensembl_prot | ENSP00000343657.6 |
mane_status | MANE Select |
chr | chr5 |
start | 71587340 |
end | 71658706 |
strand | + |
ver | v1.2 |
region | chr5:71587340-71658706 |
region5000 | chr5:71582340-71663706 |
regionname0 | MCCC2_chr5_71587340_71658706 |
regionname5000 | MCCC2_chr5_71582340_71663706 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 563 | 346 | 81 | 59 | 156 | 8 | 40 | 116 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0002 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0003 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0004 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0005 | 0/0 | 563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1692 | 296 | 58 | 48 | 148 | 6 | 35 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0002 | 1/0 | 1692 | 43 | 21 | 8 | 7 | 2 | 4 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0003 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0004 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0005 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0006 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0007 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0008 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0009 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0010 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
c0011 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1933 | 119 | 11 | 22 | 76 | 2 | 8 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0002 | 0/0 | 1933 | 107 | 16 | 18 | 56 | 2 | 15 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0003 | 1/0 | 1933 | 47 | 24 | 10 | 7 | 2 | 3 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0004 | 0/0 | 1933 | 46 | 12 | 5 | 14 | 2 | 13 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0005 | 0/0 | 1933 | 5 | 0 | 2 | 3 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0006 | 0/0 | 1933 | 4 | 4 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0007 | 0/0 | 1933 | 2 | 1 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0008 | 0/0 | 1933 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0009 | 0/0 | 1933 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0010 | 0/0 | 1933 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0011 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0012 | 0/0 | 1933 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0013 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0014 | 0/0 | 1933 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0015 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0016 | 0/0 | 1933 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0017 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0018 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0019 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0020 | 0/0 | 1933 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0021 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0022 | 0/1 | 1933 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0023 | 0/0 | 1933 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
t0024 | 0/0 | 1933 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1692 | 296 | 58 | 48 | 148 | 6 | 35 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0002 | 1/0 | 1692 | 43 | 21 | 8 | 7 | 2 | 4 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0003 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0006 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0007 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0010 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0011 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0002c0004 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0003c0008 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0004c0009 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0005c0005 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3624 | 119 | 11 | 22 | 76 | 2 | 8 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0002 | 0/0 | 3624 | 101 | 15 | 16 | 53 | 2 | 15 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0003 | 0/0 | 3624 | 4 | 3 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0004 | 0/0 | 3624 | 44 | 12 | 4 | 14 | 2 | 12 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0005 | 0/0 | 3624 | 5 | 0 | 2 | 3 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0006 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0007 | 0/0 | 3624 | 2 | 1 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0008 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0009 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0010 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0011 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0012 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0013 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0014 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0015 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0017 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0018 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0019 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0020 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0021 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0022 | 0/1 | 3624 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0001t0023 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0002t0002 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0002t0003 | 1/0 | 3624 | 40 | 19 | 8 | 7 | 2 | 3 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0002t0016 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0002t0024 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0003t0003 | 0/0 | 3624 | 3 | 2 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0006t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0007t0002 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0010t0004 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0001c0011t0004 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0002c0004t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0003c0008t0006 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0004c0009t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
a0005c0005t0002 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | copy fasta | chr5 | 71582340 | 71663706 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0012g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0014g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0017g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0019g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0020g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0021g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0022g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0001t0023g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0016g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0002t0024g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0006t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0007t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0010t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0001c0011t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0002c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0003c0008t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0004c0009t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
a0005c0005t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0193 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00140 | hp1 | a0001 | c0002 | t0003 | g0058 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0076 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00423 | hp1 | a0001 | c0001 | t0023 | g0103 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0196 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00733 | hp1 | a0001 | c0001 | t0020 | g0166 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00733 | hp2 | a0001 | c0001 | t0014 | g0256 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00741 | hp1 | a0001 | c0007 | t0002 | g0192 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0040 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0034 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01109 | hp2 | a0005 | c0005 | t0002 | g0281 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01167 | hp2 | a0001 | c0003 | t0003 | g0194 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01884 | hp1 | a0001 | c0001 | t0017 | g0011 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0086 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01978 | hp1 | a0001 | c0010 | t0004 | g0249 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01981 | hp2 | a0001 | c0002 | t0003 | g0052 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0233 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02027 | hp1 | a0001 | c0001 | t0012 | g0092 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CDX | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CDX | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02257 | hp1 | a0001 | c0001 | t0015 | g0019 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0253 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0276 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0057 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0337 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02647 | hp2 | a0001 | c0002 | t0024 | g0026 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0051 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0085 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0077 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02717 | hp2 | a0001 | c0001 | t0021 | g0228 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0079 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0278 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0047 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02809 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0234 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0235 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0036 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0242 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0049 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03098 | hp2 | a0001 | c0003 | t0003 | g0226 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0254 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03225 | hp1 | a0001 | c0003 | t0003 | g0220 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0224 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0252 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03540 | hp1 | a0003 | c0008 | t0006 | g0080 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0257 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0174 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0306 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04199 | hp1 | a0001 | c0002 | t0016 | g0053 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG04228 | hp2 | a0001 | c0011 | t0004 | g0082 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18906 | hp1 | a0001 | c0001 | t0019 | g0025 | AFR | YRI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0038 | AFR | YRI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18942 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18966 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18981 | hp1 | a0002 | c0004 | t0002 | g0332 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18982 | hp1 | a0004 | c0009 | t0002 | g0305 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18993 | hp2 | a0001 | c0006 | t0002 | g0274 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19001 | hp1 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19043 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ASW | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0251 | AFR | ASW | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0258 | EUR | TSI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0050 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0022 | g0134 | REF | REF | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0054 | REF | REF | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:71596298
|
G | A | 1 | a0002 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.215G>A | p.Arg72Gln | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/17 | 301/3624 | 215/1692 | 72/563 | chr5 | 71596298 | ||
chr5:71604443
|
T | A | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.599T>A | p.Ile200Asn | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/17 | 685/3624 | 599/1692 | 200/563 | chr5 | 71604443 | ||
chr5:71634977
|
G | T | 1 | a0004 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.838G>T | p.Asp280Tyr | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 9/17 | 924/3624 | 838/1692 | 280/563 | chr5 | 71634977 | ||
chr5:71650134
|
A | G | 1 | a0003 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1439A>G | p.Asn480Ser | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/17 | 1525/3624 | 1439/1692 | 480/563 | chr5 | 71650134 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:71587515
|
G | T | 1 | a0001c0011 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.90G>T | p.Ser30Ser | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/17 | 176/3624 | 90/1692 | 30/563 | chr5 | 71587515 | ||
chr5:71626744
|
A | C | 1 | a0001c0010 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.729A>C | p.Gly243Gly | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/17 | 815/3624 | 729/1692 | 243/563 | chr5 | 71626744 | ||
chr5:71632135
|
T | C | 1 | a0001c0006 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.753T>C | p.Thr251Thr | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/17 | 839/3624 | 753/1692 | 251/563 | chr5 | 71632135 | ||
chr5:71635216
|
T | C | 1 | a0001c0007 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.969T>C | p.Ala323Ala | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/17 | 1055/3624 | 969/1692 | 323/563 | chr5 | 71635216 | ||
chr5:71649248
|
A | G | 9 | a0001c0001a0001c0006a0001c0007others(6): Show | 304 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
synonymous_variant | LOW | c.1368A>G | p.Ala456Ala | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/17 | 1454/3624 | 1368/1692 | 456/563 | chr5 | 71649248 | ||
chr5:71656746
|
A | G | 1 | a0001c0003 | 3 | HG01167.hp2 HG03098.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1578A>G | p.Val526Val | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1664/3624 | 1578/1692 | 526/563 | chr5 | 71656746 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:71587388
|
G | A | 1 | a0001c0001t0011 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/17 | 38 | chr5 | 71587388 | |||||
chr5:71587406
|
C | G | 1 | a0001c0001t0010 | 2 | HG02622.hp1 HG03540.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/17 | chr5 | 71587406 | ||||||
chr5:71656890
|
T | C | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 30 | chr5 | 71656890 | |||||
chr5:71657038
|
T | C | 1 | a0001c0001t0013 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 178 | chr5 | 71657038 | |||||
chr5:71657051
|
A | T | 1 | a0001c0002t0024 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 191 | chr5 | 71657051 | |||||
chr5:71657064
|
T | C | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 204 | chr5 | 71657064 | |||||
chr5:71657105
|
T | C | 2 | a0001c0001t0007a0001c0001t0015 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*245T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 245 | chr5 | 71657105 | |||||
chr5:71657107
|
C | T | 21 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(18): Show | 287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*247C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 247 | chr5 | 71657107 | |||||
chr5:71657210
|
C | G | 1 | a0001c0001t0009 | 2 | HG02895.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*350C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 350 | chr5 | 71657210 | |||||
chr5:71657238
|
T | A | 1 | a0001c0002t0016 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 378 | chr5 | 71657238 | |||||
chr5:71657287
|
G | A | 1 | a0001c0001t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 427 | chr5 | 71657287 | |||||
chr5:71657386
|
C | T | 1 | a0001c0001t0015 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*526C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 526 | chr5 | 71657386 | |||||
chr5:71657437
|
T | A | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG00733.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*577T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 577 | chr5 | 71657437 | |||||
chr5:71657453
|
G | T | 3 | a0001c0001t0004a0001c0010t0004a0001c0011t0004 | 46 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*593G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 593 | chr5 | 71657453 | |||||
chr5:71657585
|
C | T | 1 | a0001c0001t0023 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*725C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 725 | chr5 | 71657585 | |||||
chr5:71657940
|
G | T | 2 | a0001c0001t0007a0001c0001t0015 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1080G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1080 | chr5 | 71657940 | |||||
chr5:71658058
|
C | T | 5 | a0001c0001t0001a0001c0001t0012a0001c0001t0020others(2): Show | 123 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1198 | chr5 | 71658058 | |||||
chr5:71658103
|
G | C | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | 293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*1243G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1243 | chr5 | 71658103 | |||||
chr5:71658207
|
C | T | 1 | a0001c0001t0008 | 2 | HG03486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1347C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1347 | chr5 | 71658207 | |||||
chr5:71658211
|
G | A | 1 | a0001c0001t0022 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1351G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1351 | chr5 | 71658211 | |||||
chr5:71658241
|
A | C | 3 | a0001c0001t0006a0001c0001t0017a0003c0008t0006 | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1381A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1381 | chr5 | 71658241 | |||||
chr5:71658326
|
T | C | 1 | a0001c0001t0005 | 5 | HG00673.hp1 HG01496.hp2 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1466T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1466 | chr5 | 71658326 | |||||
chr5:71658433
|
C | G | 5 | a0001c0001t0006a0001c0001t0014a0001c0001t0017others(2): Show | 7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1573C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1573 | chr5 | 71658433 | |||||
chr5:71658564
|
G | A | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1704G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1704 | chr5 | 71658564 | |||||
chr5:71658664
|
A | G | 1 | a0001c0001t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1804A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1804 | chr5 | 71658664 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:71587938
|
A | G | 1 | a0001c0001t0010g0337 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129+384A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71587938 | ||||||
chr5:71588078
|
G | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0329a0001c0001t0002g0330others(6): Show | 11 | HG02056.hp2 NA18950.hp2 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+524G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588078 | ||||||
chr5:71588138
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.129+584G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588138 | ||||||
chr5:71588172
|
G | A | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+618G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588172 | ||||||
chr5:71588229
|
A | G | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+675A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588229 | ||||||
chr5:71588268
|
C | CA | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG02109.hp1 HG04204.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+734dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71588268 | |||||
chr5:71588268
|
CA | C | 137 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(134): Show | 143 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.129+734delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71588268 | |||||
chr5:71588419
|
C | A | 1 | a0001c0001t0004g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.129+865C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588419 | ||||||
chr5:71588487
|
A | G | 3 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0328 | 3 | HG00438.hp2 HG02040.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.129+933A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588487 | ||||||
chr5:71588547
|
C | T | 140 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(137): Show | 146 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.129+993C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588547 | ||||||
chr5:71588670
|
T | C | 1 | a0001c0001t0015g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129+1116T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588670 | ||||||
chr5:71588675
|
A | T | 92 | a0001c0001t0001g0261a0001c0001t0001g0296a0001c0001t0001g0297others(89): Show | 97 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.129+1121A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588675 | ||||||
chr5:71588735
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.129+1181G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588735 | ||||||
chr5:71588860
|
G | C | 132 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(129): Show | 138 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.129+1306G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588860 | ||||||
chr5:71589020
|
A | G | 2 | a0001c0002t0003g0002a0001c0002t0003g0193 | 4 | HG00099.hp2 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1466A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589020 | ||||||
chr5:71589208
|
T | G | 140 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(137): Show | 146 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.129+1654T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589208 | ||||||
chr5:71589421
|
C | T | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+1867C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589421 | ||||||
chr5:71589566
|
A | C | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129+2012A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589566 | ||||||
chr5:71589585
|
T | C | 123 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(120): Show | 129 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.129+2031T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589585 | ||||||
chr5:71589711
|
T | C | 133 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(130): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.129+2157T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589711 | ||||||
chr5:71589776
|
T | C | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129+2222T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589776 | ||||||
chr5:71589791
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 122 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.129+2237A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589791 | ||||||
chr5:71590096
|
C | A | 1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.129+2542C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590096 | ||||||
chr5:71590097
|
G | T | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+2543G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590097 | ||||||
chr5:71590109
|
A | AAC | 10 | a0001c0001t0002g0241a0001c0001t0004g0195a0001c0001t0004g0206others(7): Show | 10 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+2575_129+2576d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71590109 | |||||
chr5:71590109
|
AAC | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 137 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.129+2575_129+2576d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71590109 | |||||
chr5:71590146
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.129+2592C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590146 | ||||||
chr5:71590312
|
T | A | 122 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(119): Show | 128 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.130-2614T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590312 | ||||||
chr5:71590553
|
A | C | 1 | a0001c0001t0009g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.130-2373A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590553 | ||||||
chr5:71590554
|
G | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.130-2372G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590554 | ||||||
chr5:71590809
|
T | G | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130-2117T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590809 | ||||||
chr5:71590816
|
C | CA | 118 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(115): Show | 124 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.130-2096dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71590816 | |||||
chr5:71591105
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.130-1821A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591105 | ||||||
chr5:71591363
|
A | C | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130-1563A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591363 | ||||||
chr5:71591434
|
GT | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.130-1473delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71591434 | |||||
chr5:71591464
|
T | G | 1 | a0001c0001t0015g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130-1462T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591464 | ||||||
chr5:71591626
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.130-1300G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591626 | ||||||
chr5:71591628
|
G | A | 3 | a0001c0001t0001g0218a0001c0002t0003g0217a0001c0002t0003g0219 | 3 | NA18747.hp2 NA18945.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.130-1298G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591628 | ||||||
chr5:71591633
|
C | G | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG00673.hp2 NA18986.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1293C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591633 | ||||||
chr5:71591662
|
C | T | 4 | a0001c0001t0007g0196a0001c0001t0010g0257a0001c0001t0010g0337others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1264C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591662 | ||||||
chr5:71591668
|
C | T | 2 | a0001c0002t0003g0085a0001c0002t0003g0254 | 2 | HG02698.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.130-1258C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591668 | ||||||
chr5:71591732
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.130-1194T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591732 | ||||||
chr5:71591734
|
G | A | 1 | a0001c0002t0003g0022 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130-1192G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591734 | ||||||
chr5:71592020
|
C | T | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130-906C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592020 | ||||||
chr5:71592296
|
G | A | 5 | a0001c0001t0007g0196a0001c0001t0010g0257a0001c0001t0010g0337others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-630G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592296 | ||||||
chr5:71592397
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.130-529A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592397 | ||||||
chr5:71592415
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.130-511A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592415 | ||||||
chr5:71592838
|
G | GT | 26 | a0001c0001t0001g0017a0001c0001t0001g0176a0001c0001t0001g0177others(23): Show | 26 | HG00544.hp2 HG00735.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-72dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71592838 | |||||
chr5:71592847
|
T | C | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130-79T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592847 | ||||||
chr5:71593069
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.196+77A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593069 | ||||||
chr5:71593081
|
C | T | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.196+89C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593081 | ||||||
chr5:71593086
|
G | GAT | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0181others(1): Show | 4 | HG00544.hp2 HG02071.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+97_196+98dupAT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71593086 | |||||
chr5:71593090
|
T | TA | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.196+98_196+99insA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593090 | ||||||
chr5:71593091
|
T | A | 2 | a0001c0001t0007g0253a0001c0002t0003g0023 | 2 | HG01069.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.196+99T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593091 | ||||||
chr5:71593092
|
T | A | 2 | a0001c0001t0002g0021a0001c0001t0015g0019 | 2 | HG01243.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.196+100T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593092 | ||||||
chr5:71593094
|
T | A | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196+102T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593094 | ||||||
chr5:71593096
|
T | A | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196+104T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593096 | ||||||
chr5:71593298
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.196+306C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593298 | ||||||
chr5:71593495
|
G | A | 1 | a0001c0001t0015g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+503G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593495 | ||||||
chr5:71593500
|
GA | G | 2 | a0001c0002t0003g0002a0001c0002t0003g0193 | 4 | HG00099.hp2 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+512delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71593500 | |||||
chr5:71593585
|
C | T | 4 | a0001c0001t0001g0314a0001c0001t0001g0317a0001c0001t0002g0315others(1): Show | 4 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+593C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593585 | ||||||
chr5:71593790
|
A | G | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+798A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593790 | ||||||
chr5:71593960
|
C | T | 4 | a0001c0001t0007g0196a0001c0001t0010g0257a0001c0001t0010g0337others(1): Show | 4 | HG00642.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+968C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593960 | ||||||
chr5:71594043
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.196+1051G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594043 | ||||||
chr5:71594178
|
A | T | 4 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+1186A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594178 | ||||||
chr5:71594522
|
C | T | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.196+1530C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594522 | ||||||
chr5:71594527
|
C | CA | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.196+1551dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71594527 | |||||
chr5:71594565
|
A | C | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+1573A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594565 | ||||||
chr5:71594569
|
T | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.196+1577T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594569 | ||||||
chr5:71594586
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196+1594A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594586 | ||||||
chr5:71594624
|
G | A | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+1632G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594624 | ||||||
chr5:71594625
|
T | C | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.196+1633T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594625 | ||||||
chr5:71594897
|
TC | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.197-1382delC | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594897 | ||||||
chr5:71594898
|
C | CT | 9 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(6): Show | 9 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-1367dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71594898 | |||||
chr5:71594898
|
C | T | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.197-1382C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594898 | ||||||
chr5:71594939
|
C | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0214others(1): Show | 4 | HG00733.hp1 HG01099.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1341C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594939 | ||||||
chr5:71594961
|
C | T | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.197-1319C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594961 | ||||||
chr5:71594985
|
G | GC | 247 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.197-1289dupC | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71594985 | |||||
chr5:71595072
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.197-1208A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595072 | ||||||
chr5:71595106
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.197-1174T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595106 | ||||||
chr5:71595428
|
C | CA | 44 | a0001c0001t0001g0218a0001c0001t0002g0008a0001c0001t0002g0021others(41): Show | 45 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-834dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | |||||
chr5:71595428
|
C | CAA | 94 | a0001c0001t0001g0018a0001c0001t0001g0160a0001c0001t0001g0161others(91): Show | 99 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.197-835_197-834dup others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | |||||
chr5:71595428
|
C | CAAA | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 110 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.197-836_197-834dup others(3): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | |||||
chr5:71595428
|
C | CAAAA | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0176others(3): Show | 6 | HG02027.hp1 HG03927.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-837_197-834dup others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | |||||
chr5:71595856
|
C | G | 7 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0075others(4): Show | 7 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-424C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595856 | ||||||
chr5:71595913
|
A | T | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-367A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595913 | ||||||
chr5:71596079
|
A | AT | 113 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.197-192dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71596079 | |||||
chr5:71596200
|
GATTAAGT | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.197-75_197-69delAG others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71596200 | |||||
chr5:71596659
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.281+295T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596659 | ||||||
chr5:71596664
|
G | C | 1 | a0001c0001t0002g0003 | 3 | HG00280.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.281+300G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596664 | ||||||
chr5:71596811
|
G | A | 1 | a0001c0002t0024g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281+447G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596811 | ||||||
chr5:71596896
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.281+532T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596896 | ||||||
chr5:71596939
|
C | A | 1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.281+575C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596939 | ||||||
chr5:71596939
|
CA | C | 29 | a0001c0001t0001g0071a0001c0001t0002g0061a0001c0001t0002g0062others(26): Show | 29 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.281+587delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71596939 | |||||
chr5:71596981
|
T | C | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281+617T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596981 | ||||||
chr5:71597036
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.281+672T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597036 | ||||||
chr5:71597228
|
T | C | 1 | a0001c0002t0003g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.281+864T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597228 | ||||||
chr5:71597385
|
A | C | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281+1021A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597385 | ||||||
chr5:71597511
|
G | C | 2 | a0001c0001t0001g0261a0001c0001t0002g0260 | 2 | HG01123.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.281+1147G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597511 | ||||||
chr5:71597524
|
C | CATAGGGT others(40): Show |
1 | a0001c0011t0004g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.281+1163_281+1209d others(49): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71597524 | |||||
chr5:71597529
|
GGTA | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.281+1174_281+1176d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71597529 | |||||
chr5:71597635
|
A | G | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.281+1271A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597635 | ||||||
chr5:71597932
|
C | T | 1 | a0001c0002t0003g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.281+1568C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597932 | ||||||
chr5:71598071
|
C | CT | 17 | a0001c0001t0001g0071a0001c0001t0001g0183a0001c0001t0001g0218others(14): Show | 17 | HG00140.hp1 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.282-1568dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598071 | |||||
chr5:71598079
|
T | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0317 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.282-1580T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598079 | ||||||
chr5:71598136
|
G | A | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.282-1523G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598136 | ||||||
chr5:71598180
|
T | C | 4 | a0001c0001t0001g0314a0001c0001t0001g0317a0001c0001t0002g0315others(1): Show | 4 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-1479T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598180 | ||||||
chr5:71598337
|
G | A | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.282-1322G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598337 | ||||||
chr5:71598368
|
G | A | 1 | a0001c0003t0003g0220 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282-1291G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598368 | ||||||
chr5:71598378
|
T | A | 1 | a0001c0001t0015g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282-1281T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598378 | ||||||
chr5:71598417
|
A | G | 1 | a0001c0001t0020g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.282-1242A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598417 | ||||||
chr5:71598444
|
A | T | 23 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(20): Show | 23 | HG00642.hp1 HG00741.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.282-1215A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598444 | ||||||
chr5:71598448
|
T | A | 91 | a0001c0001t0001g0261a0001c0001t0001g0296a0001c0001t0001g0297others(88): Show | 96 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.282-1211T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598448 | ||||||
chr5:71598464
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.282-1195G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598464 | ||||||
chr5:71598474
|
C | G | 5 | a0001c0001t0001g0163a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG00673.hp2 NA18971.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1185C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598474 | ||||||
chr5:71598533
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.282-1126G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598533 | ||||||
chr5:71598606
|
A | AT | 12 | a0001c0001t0001g0317a0001c0001t0002g0202a0001c0001t0002g0205others(9): Show | 12 | HG00621.hp2 HG01168.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-1032dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | |||||
chr5:71598606
|
AT | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 137 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.282-1032delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | |||||
chr5:71598606
|
ATT | A | 7 | a0001c0001t0001g0094a0001c0001t0001g0186a0001c0001t0004g0209others(4): Show | 7 | HG00741.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-1033_282-1032d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | |||||
chr5:71598606
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.282-1041_282-1032d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | |||||
chr5:71598910
|
C | G | 1 | a0001c0002t0003g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.282-749C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598910 | ||||||
chr5:71598926
|
A | AT | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 120 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.282-720dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598926 | |||||
chr5:71598958
|
C | T | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.282-701C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598958 | ||||||
chr5:71599133
|
C | T | 120 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(117): Show | 126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.282-526C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599133 | ||||||
chr5:71599136
|
G | A | 5 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0269others(2): Show | 5 | HG02155.hp1 NA18989.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-523G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599136 | ||||||
chr5:71599146
|
T | C | 4 | a0001c0001t0001g0218a0001c0002t0003g0217a0001c0002t0003g0219others(1): Show | 4 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-513T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599146 | ||||||
chr5:71599238
|
C | T | 9 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.282-421C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599238 | ||||||
chr5:71599300
|
G | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0214a0001c0001t0020g0166 | 3 | HG00733.hp1 HG01261.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.282-359G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599300 | ||||||
chr5:71599325
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 122 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.282-334G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599325 | ||||||
chr5:71599436
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.282-223C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599436 | ||||||
chr5:71599451
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.282-208T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599451 | ||||||
chr5:71599601
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.282-58G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599601 | ||||||
chr5:71599901
|
C | T | 1 | a0001c0001t0002g0328 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.383+141C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71599901 | ||||||
chr5:71600022
|
C | T | 3 | a0001c0001t0002g0227a0001c0001t0017g0011a0001c0001t0021g0228 | 3 | HG01884.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383+262C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600022 | ||||||
chr5:71600077
|
A | T | 2 | a0001c0001t0002g0227a0001c0001t0021g0228 | 2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383+317A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600077 | ||||||
chr5:71600079
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383+319C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600079 | ||||||
chr5:71600158
|
C | T | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.383+398C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600158 | ||||||
chr5:71600196
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0177 | 2 | HG03927.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.383+436G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600196 | ||||||
chr5:71600301
|
T | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(320): Show | 334 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.383+541T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600301 | ||||||
chr5:71600399
|
C | T | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.383+639C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600399 | ||||||
chr5:71600564
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.383+804C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600564 | ||||||
chr5:71600749
|
T | A | 1 | a0001c0001t0004g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.383+989T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600749 | ||||||
chr5:71601126
|
A | C | 1 | a0001c0001t0015g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.383+1366A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601126 | ||||||
chr5:71601228
|
C | T | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.384-1278C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601228 | ||||||
chr5:71601426
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0151others(5): Show | 8 | HG02040.hp2 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-1080C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601426 | ||||||
chr5:71601574
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.384-932C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601574 | ||||||
chr5:71601624
|
G | T | 112 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(109): Show | 118 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.384-882G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601624 | ||||||
chr5:71601733
|
T | C | 2 | a0001c0001t0007g0196a0001c0001t0017g0011 | 2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.384-773T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601733 | ||||||
chr5:71601844
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0151a0001c0001t0001g0152 | 3 | HG02080.hp1 NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.384-662G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601844 | ||||||
chr5:71602129
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.384-377G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602129 | ||||||
chr5:71602217
|
A | G | 2 | a0001c0001t0002g0301a0001c0001t0002g0302 | 2 | NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.384-289A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602217 | ||||||
chr5:71602426
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.384-80T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602426 | ||||||
chr5:71602463
|
A | G | 4 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-43A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602463 | ||||||
chr5:71602837
|
A | G | 1 | a0001c0001t0002g0323 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.511+204A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71602837 | ||||||
chr5:71602839
|
A | G | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.511+206A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71602839 | ||||||
chr5:71602848
|
C | T | 4 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0248others(1): Show | 4 | HG01433.hp2 HG01978.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+215C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71602848 | ||||||
chr5:71603040
|
T | G | 2 | a0001c0001t0007g0196a0001c0001t0017g0011 | 2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.511+407T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603040 | ||||||
chr5:71603150
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.511+517C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603150 | ||||||
chr5:71603287
|
G | A | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.511+654G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603287 | ||||||
chr5:71603407
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 148 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.511+774G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603407 | ||||||
chr5:71603411
|
G | T | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511+778G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603411 | ||||||
chr5:71603415
|
CA | C | 133 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0097others(130): Show | 140 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.511+806delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr5 | 71603415 | |||||
chr5:71603415
|
CAA | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0015others(127): Show | 133 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.511+805_511+806del others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr5 | 71603415 | |||||
chr5:71603469
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(301): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.511+836A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603469 | ||||||
chr5:71603485
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0225a0001c0003t0003g0194others(2): Show | 6 | HG01167.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.511+852C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603485 | ||||||
chr5:71603692
|
C | G | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.512-664C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603692 | ||||||
chr5:71603811
|
G | T | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.512-545G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603811 | ||||||
chr5:71603854
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.512-502C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603854 | ||||||
chr5:71604109
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.512-247G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71604109 | ||||||
chr5:71604165
|
T | A | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.512-191T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71604165 | ||||||
chr5:71604242
|
G | A | 11 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(8): Show | 11 | HG00741.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.512-114G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71604242 | ||||||
chr5:71604525
|
G | T | 9 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+57G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604525 | ||||||
chr5:71604582
|
C | CT | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 126 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.624+128dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71604582 | |||||
chr5:71604582
|
CT | C | 14 | a0001c0001t0001g0071a0001c0001t0001g0213a0001c0001t0002g0061others(11): Show | 14 | HG01070.hp2 HG01123.hp2 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.624+128delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71604582 | |||||
chr5:71604730
|
G | A | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+262G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604730 | ||||||
chr5:71604734
|
C | T | 1 | a0003c0008t0006g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.624+266C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604734 | ||||||
chr5:71604752
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.624+284C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604752 | ||||||
chr5:71604910
|
C | T | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.624+442C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604910 | ||||||
chr5:71605030
|
C | T | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+562C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605030 | ||||||
chr5:71605031
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.624+563G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605031 | ||||||
chr5:71605043
|
C | T | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.624+575C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605043 | ||||||
chr5:71605052
|
GT | G | 125 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(122): Show | 131 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.624+585delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605052 | ||||||
chr5:71605112
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(249): Show | 262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.624+644A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605112 | ||||||
chr5:71605166
|
G | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.624+698G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605166 | ||||||
chr5:71605235
|
C | A | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+767C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605235 | ||||||
chr5:71605426
|
G | T | 1 | a0001c0001t0002g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.624+958G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605426 | ||||||
chr5:71605520
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0023g0103 | 2 | HG00423.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.624+1052T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605520 | ||||||
chr5:71605536
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.624+1068C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605536 | ||||||
chr5:71605580
|
T | G | 1 | a0001c0002t0003g0012 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.624+1112T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605580 | ||||||
chr5:71605634
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(290): Show | 303 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.624+1166C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605634 | ||||||
chr5:71605653
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.624+1185C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605653 | ||||||
chr5:71605662
|
G | C | 8 | a0001c0001t0004g0195a0001c0001t0004g0206a0001c0001t0004g0236others(5): Show | 8 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.624+1194G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605662 | ||||||
chr5:71605930
|
C | T | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+1462C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605930 | ||||||
chr5:71606050
|
C | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0147a0001c0001t0001g0167others(1): Show | 4 | HG03927.hp2 NA18612.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1582C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606050 | ||||||
chr5:71606068
|
G | C | 1 | a0001c0010t0004g0249 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.624+1600G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606068 | ||||||
chr5:71606129
|
G | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.624+1661G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606129 | ||||||
chr5:71606189
|
G | C | 1 | a0001c0001t0004g0267 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.624+1721G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606189 | ||||||
chr5:71606654
|
A | T | 1 | a0001c0001t0004g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.624+2186A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606654 | ||||||
chr5:71606759
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.624+2291T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606759 | ||||||
chr5:71606760
|
A | C | 1 | a0001c0002t0003g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.624+2292A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606760 | ||||||
chr5:71606761
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.624+2293A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606761 | ||||||
chr5:71606840
|
G | A | 11 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(8): Show | 11 | HG00741.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2372G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606840 | ||||||
chr5:71606904
|
C | G | 1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624+2436C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606904 | ||||||
chr5:71607059
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.624+2591C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607059 | ||||||
chr5:71607091
|
A | C | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+2623A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607091 | ||||||
chr5:71607092
|
A | C | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+2624A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607092 | ||||||
chr5:71607125
|
T | C | 2 | a0001c0001t0004g0246a0001c0001t0004g0247 | 2 | HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.624+2657T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607125 | ||||||
chr5:71607131
|
G | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0273a0001c0001t0002g0275others(3): Show | 7 | HG01346.hp1 HG03239.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+2663G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607131 | ||||||
chr5:71607163
|
T | C | 2 | a0001c0001t0002g0221a0001c0001t0002g0229 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.624+2695T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607163 | ||||||
chr5:71607277
|
A | T | 1 | a0001c0001t0004g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.624+2809A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607277 | ||||||
chr5:71607292
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.624+2824G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607292 | ||||||
chr5:71607362
|
G | A | 2 | a0001c0001t0001g0190a0001c0002t0003g0254 | 2 | HG03130.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.624+2894G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607362 | ||||||
chr5:71607491
|
C | T | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+3023C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607491 | ||||||
chr5:71607498
|
T | A | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+3030T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607498 | ||||||
chr5:71607662
|
T | G | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+3194T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607662 | ||||||
chr5:71607669
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.624+3201A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607669 | ||||||
chr5:71607732
|
C | T | 126 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(123): Show | 132 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.624+3264C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607732 | ||||||
chr5:71607750
|
C | T | 126 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(123): Show | 132 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.624+3282C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607750 | ||||||
chr5:71607840
|
G | A | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+3372G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607840 | ||||||
chr5:71607881
|
C | T | 113 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(110): Show | 119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.624+3413C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607881 | ||||||
chr5:71607882
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.624+3414A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607882 | ||||||
chr5:71607955
|
C | T | 8 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+3487C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607955 | ||||||
chr5:71608047
|
A | G | 2 | a0001c0002t0003g0041a0001c0002t0003g0042 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.624+3579A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608047 | ||||||
chr5:71608093
|
C | T | 2 | a0001c0001t0007g0253a0001c0002t0003g0224 | 2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.624+3625C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608093 | ||||||
chr5:71608248
|
C | A | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+3780C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608248 | ||||||
chr5:71608294
|
C | G | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+3826C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608294 | ||||||
chr5:71608397
|
A | G | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+3929A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608397 | ||||||
chr5:71608554
|
T | C | 2 | a0001c0001t0007g0196a0001c0001t0017g0011 | 2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.624+4086T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608554 | ||||||
chr5:71608632
|
G | C | 8 | a0001c0002t0003g0002a0001c0002t0003g0023a0001c0002t0003g0051others(5): Show | 10 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.624+4164G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608632 | ||||||
chr5:71608756
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.624+4288C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608756 | ||||||
chr5:71608896
|
C | T | 1 | a0001c0002t0024g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.624+4428C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608896 | ||||||
chr5:71608930
|
G | A | 1 | a0001c0001t0005g0276 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.624+4462G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608930 | ||||||
chr5:71608957
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.624+4489C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608957 | ||||||
chr5:71609000
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.624+4532A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609000 | ||||||
chr5:71609117
|
C | T | 1 | a0001c0001t0004g0101 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.624+4649C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609117 | ||||||
chr5:71609160
|
T | G | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+4692T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609160 | ||||||
chr5:71609186
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624+4718C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609186 | ||||||
chr5:71609257
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+4789T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609257 | ||||||
chr5:71609267
|
C | G | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.624+4799C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609267 | ||||||
chr5:71609301
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.624+4833G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609301 | ||||||
chr5:71609388
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.624+4920G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609388 | ||||||
chr5:71609482
|
A | G | 4 | a0001c0001t0004g0033a0001c0001t0004g0068a0001c0001t0004g0174others(1): Show | 4 | HG02056.hp1 HG02080.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+5014A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609482 | ||||||
chr5:71609582
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.624+5114C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609582 | ||||||
chr5:71609802
|
T | C | 1 | a0001c0001t0004g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.624+5334T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609802 | ||||||
chr5:71609817
|
A | G | 1 | a0001c0001t0004g0105 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.624+5349A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609817 | ||||||
chr5:71609827
|
G | A | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+5359G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609827 | ||||||
chr5:71609834
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0019g0025 | 2 | HG01978.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.624+5366A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609834 | ||||||
chr5:71609850
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.624+5382G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609850 | ||||||
chr5:71609922
|
C | T | 27 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0200others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.624+5454C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609922 | ||||||
chr5:71610067
|
G | T | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+5599G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610067 | ||||||
chr5:71610091
|
C | T | 1 | a0001c0001t0004g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.624+5623C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610091 | ||||||
chr5:71610119
|
T | G | 10 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+5651T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610119 | ||||||
chr5:71610170
|
G | A | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+5702G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610170 | ||||||
chr5:71610224
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.624+5756C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610224 | ||||||
chr5:71610231
|
G | T | 1 | a0001c0001t0001g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.624+5763G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610231 | ||||||
chr5:71610249
|
G | T | 116 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(113): Show | 122 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.624+5781G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610249 | ||||||
chr5:71610301
|
G | A | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+5833G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610301 | ||||||
chr5:71610325
|
G | A | 2 | a0001c0001t0007g0196a0001c0001t0017g0011 | 2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.624+5857G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610325 | ||||||
chr5:71610335
|
G | A | 1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624+5867G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610335 | ||||||
chr5:71610407
|
T | C | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.624+5939T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610407 | ||||||
chr5:71610440
|
C | T | 2 | a0001c0001t0004g0245a0001c0001t0004g0250 | 2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.624+5972C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610440 | ||||||
chr5:71610541
|
G | A | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.624+6073G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610541 | ||||||
chr5:71610558
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.624+6090G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610558 | ||||||
chr5:71610567
|
C | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(7): Show | 12 | HG00544.hp2 HG01257.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.624+6099C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610567 | ||||||
chr5:71610570
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(7): Show | 12 | HG00544.hp2 HG01257.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.624+6102A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610570 | ||||||
chr5:71610725
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.624+6257G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610725 | ||||||
chr5:71610814
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.624+6346G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610814 | ||||||
chr5:71610846
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.624+6378C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610846 | ||||||
chr5:71610858
|
T | C | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+6390T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610858 | ||||||
chr5:71610863
|
G | A | 4 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+6395G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610863 | ||||||
chr5:71610992
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.624+6524C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610992 | ||||||
chr5:71610999
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.624+6531C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610999 | ||||||
chr5:71611021
|
G | A | 1 | a0001c0001t0005g0272 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.624+6553G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611021 | ||||||
chr5:71611280
|
A | G | 8 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245others(5): Show | 8 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+6812A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611280 | ||||||
chr5:71611345
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.624+6877C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611345 | ||||||
chr5:71611346
|
G | A | 2 | a0001c0001t0002g0021a0001c0001t0015g0019 | 2 | HG01243.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.624+6878G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611346 | ||||||
chr5:71611403
|
C | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 148 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.624+6935C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611403 | ||||||
chr5:71611422
|
A | G | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+6954A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611422 | ||||||
chr5:71611552
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0180 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.624+7084C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611552 | ||||||
chr5:71611610
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+7142T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611610 | ||||||
chr5:71611631
|
G | A | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+7163G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611631 | ||||||
chr5:71611668
|
G | A | 115 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(112): Show | 121 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.624+7200G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611668 | ||||||
chr5:71611697
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.624+7229G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611697 | ||||||
chr5:71611711
|
G | A | 115 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(112): Show | 121 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.624+7243G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611711 | ||||||
chr5:71611799
|
T | G | 7 | a0001c0002t0003g0027a0001c0002t0003g0028a0001c0002t0003g0029others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+7331T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611799 | ||||||
chr5:71611838
|
G | T | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+7370G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611838 | ||||||
chr5:71611881
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.624+7413C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611881 | ||||||
chr5:71611890
|
G | A | 1 | a0001c0001t0004g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+7422G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611890 | ||||||
chr5:71611986
|
C | T | 1 | a0001c0001t0007g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+7518C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611986 | ||||||
chr5:71612030
|
T | C | 4 | a0001c0001t0001g0314a0001c0001t0001g0317a0001c0001t0002g0315others(1): Show | 4 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+7562T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612030 | ||||||
chr5:71612033
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.624+7565C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612033 | ||||||
chr5:71612055
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.624+7587C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612055 | ||||||
chr5:71612159
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.624+7691T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612159 | ||||||
chr5:71612321
|
A | T | 1 | a0001c0001t0004g0245 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.624+7853A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612321 | ||||||
chr5:71612390
|
G | A | 11 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(8): Show | 11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+7922G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612390 | ||||||
chr5:71612443
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.624+7975C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612443 | ||||||
chr5:71612472
|
G | A | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.624+8004G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612472 | ||||||
chr5:71612526
|
A | G | 1 | a0001c0001t0002g0288 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.624+8058A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612526 | ||||||
chr5:71612665
|
C | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 150 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.624+8197C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612665 | ||||||
chr5:71613268
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.624+8800A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71613268 | ||||||
chr5:71613415
|
A | T | 11 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(8): Show | 11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+8947A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71613415 | ||||||
chr5:71613521
|
C | T | 11 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(8): Show | 11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+9053C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71613521 | ||||||
chr5:71614029
|
T | TACACAC | 14 | a0001c0001t0001g0104a0001c0001t0002g0323a0001c0001t0004g0059others(11): Show | 14 | HG00642.hp1 HG01099.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.624+9577_624+9582d others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | |||||
chr5:71614029
|
T | TACACACA others(1): Show |
16 | a0001c0001t0001g0087a0001c0001t0001g0141a0001c0001t0001g0145others(13): Show | 16 | HG00673.hp2 HG01243.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.624+9575_624+9582d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | |||||
chr5:71614029
|
T | TACACACA others(3): Show |
110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 114 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.624+9573_624+9582d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | |||||
chr5:71614029
|
T | TACACACA others(5): Show |
113 | a0001c0001t0001g0018a0001c0001t0001g0091a0001c0001t0001g0097others(110): Show | 119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.624+9571_624+9582d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | |||||
chr5:71614029
|
T | TACACACA others(7): Show |
15 | a0001c0001t0001g0215a0001c0001t0002g0197a0001c0001t0002g0202others(12): Show | 15 | HG00735.hp1 HG01167.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.624+9569_624+9582d others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | |||||
chr5:71614029
|
T | TACACACA others(9): Show |
1 | a0001c0001t0002g0326 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.624+9567_624+9582d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | |||||
chr5:71614359
|
G | A | 1 | a0005c0005t0002g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.624+9891G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71614359 | ||||||
chr5:71614442
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 271 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.624+9974T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71614442 | ||||||
chr5:71614484
|
C | CT | 120 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(117): Show | 125 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.624+10031dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614484 | |||||
chr5:71614484
|
C | CTTT | 9 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(6): Show | 9 | HG01433.hp2 HG01978.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+10029_624+1003 others(7): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614484 | |||||
chr5:71614484
|
CT | C | 8 | a0001c0001t0001g0095a0001c0001t0002g0290a0001c0001t0004g0209others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.624+10031delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614484 | |||||
chr5:71614922
|
C | G | 1 | a0001c0001t0004g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+10454C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71614922 | ||||||
chr5:71615035
|
C | T | 1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624+10567C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615035 | ||||||
chr5:71615166
|
C | T | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.624+10698C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615166 | ||||||
chr5:71615323
|
C | T | 11 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(8): Show | 11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+10855C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615323 | ||||||
chr5:71615532
|
C | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.624+11064C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615532 | ||||||
chr5:71615570
|
G | A | 11 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(8): Show | 11 | HG00741.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-11070G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615570 | ||||||
chr5:71615696
|
C | G | 1 | a0001c0001t0002g0287 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.625-10944C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615696 | ||||||
chr5:71615732
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-10908C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615732 | ||||||
chr5:71615956
|
G | A | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-10684G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615956 | ||||||
chr5:71615967
|
A | G | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.625-10673A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615967 | ||||||
chr5:71616110
|
T | C | 1 | a0001c0002t0003g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.625-10530T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616110 | ||||||
chr5:71616120
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 150 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.625-10520C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616120 | ||||||
chr5:71616162
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.625-10478C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616162 | ||||||
chr5:71616666
|
G | C | 5 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0048others(2): Show | 5 | HG00741.hp2 HG02258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-9974G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616666 | ||||||
chr5:71616676
|
T | C | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-9964T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616676 | ||||||
chr5:71616716
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.625-9924C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616716 | ||||||
chr5:71616854
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 151 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.625-9786C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616854 | ||||||
chr5:71616982
|
A | G | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-9658A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616982 | ||||||
chr5:71617042
|
CA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-9594delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71617042 | |||||
chr5:71617227
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.625-9413T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617227 | ||||||
chr5:71617471
|
C | T | 2 | a0001c0003t0003g0194a0001c0003t0003g0226 | 2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.625-9169C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617471 | ||||||
chr5:71617612
|
T | C | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.625-9028T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617612 | ||||||
chr5:71617854
|
A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 150 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.625-8786A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617854 | ||||||
chr5:71618081
|
G | C | 115 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(112): Show | 121 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.625-8559G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618081 | ||||||
chr5:71618236
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.625-8404T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618236 | ||||||
chr5:71618437
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 151 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.625-8203C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618437 | ||||||
chr5:71618462
|
ATTCT | A | 10 | a0001c0001t0001g0261a0001c0001t0002g0003a0001c0001t0002g0198others(7): Show | 12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-8166_625-8163d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618462 | |||||
chr5:71618488
|
T | TCTTC | 9 | a0001c0001t0002g0271a0001c0001t0002g0287a0001c0001t0002g0316others(6): Show | 10 | HG01074.hp1 HG01109.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-8092_625-8089d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
T | TCTTCCTT others(1): Show |
5 | a0001c0001t0002g0320a0001c0002t0003g0027a0001c0002t0003g0037others(2): Show | 5 | HG02074.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-8096_625-8089d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
T | TCTTCCTT others(5): Show |
1 | a0001c0002t0003g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.625-8100_625-8089d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTC | T | 45 | a0001c0001t0001g0314a0001c0001t0001g0317a0001c0001t0001g0318others(42): Show | 49 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.625-8092_625-8089d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(1): Show |
T | 48 | a0001c0001t0001g0071a0001c0001t0001g0218a0001c0001t0001g0296others(45): Show | 49 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.625-8096_625-8089d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(5): Show |
T | 46 | a0001c0001t0001g0261a0001c0001t0002g0009a0001c0001t0002g0061others(43): Show | 47 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.625-8100_625-8089d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(9): Show |
T | 9 | a0001c0001t0002g0231a0001c0001t0002g0286a0001c0001t0002g0307others(6): Show | 9 | HG01168.hp1 HG01358.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-8104_625-8089d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(13): Show |
T | 8 | a0001c0001t0002g0222a0001c0001t0002g0227a0001c0001t0002g0300others(5): Show | 8 | HG01261.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.625-8108_625-8089d others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(17): Show |
T | 3 | a0001c0001t0006g0024a0001c0001t0006g0208a0001c0001t0007g0196 | 3 | HG00642.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.625-8112_625-8089d others(26): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(21): Show |
T | 13 | a0001c0001t0001g0102a0001c0001t0001g0112a0001c0001t0002g0093others(10): Show | 13 | HG00280.hp1 HG01433.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.625-8116_625-8089d others(30): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(25): Show |
T | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-8120_625-8089d others(34): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(29): Show |
T | 1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.625-8124_625-8089d others(38): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618488
|
TCTTCCTT others(37): Show |
T | 1 | a0003c0008t0006g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-8132_625-8089d others(46): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | |||||
chr5:71618494
|
TTCCTTCC others(3): Show |
T | 1 | a0001c0001t0006g0207 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.625-8145_625-8136d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618494 | ||||||
chr5:71618501
|
C | CTTCCTTC others(5): Show |
1 | a0001c0002t0003g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.625-8128_625-8127i others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618501 | |||||
chr5:71618503
|
T | TCCTTCCT others(5): Show |
1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.625-8126_625-8125i others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618503 | |||||
chr5:71618512
|
CCTTCCTT others(33): Show |
C | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.625-8124_625-8085d others(42): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618512 | |||||
chr5:71618548
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 152 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.625-8092C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618548 | ||||||
chr5:71618548
|
CCTTT | C | 3 | a0001c0002t0003g0002a0001c0002t0003g0052a0001c0002t0003g0193 | 5 | HG00099.hp2 HG01255.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-8081_625-8078d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618548 | |||||
chr5:71618552
|
T | C | 3 | a0001c0002t0003g0023a0001c0002t0003g0051a0001c0002t0003g0058 | 3 | HG00140.hp1 HG01069.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.625-8088T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618552 | ||||||
chr5:71618607
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.625-8033G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618607 | ||||||
chr5:71618624
|
T | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.625-8016T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618624 | ||||||
chr5:71618655
|
G | A | 10 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-7985G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618655 | ||||||
chr5:71619117
|
C | T | 3 | a0001c0001t0010g0257a0001c0001t0010g0337a0001c0002t0003g0254 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-7523C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619117 | ||||||
chr5:71619227
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.625-7413A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619227 | ||||||
chr5:71619256
|
T | G | 1 | a0001c0002t0003g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.625-7384T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619256 | ||||||
chr5:71619346
|
C | T | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.625-7294C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619346 | ||||||
chr5:71619583
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-7057C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619583 | ||||||
chr5:71619661
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-6979G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619661 | ||||||
chr5:71619718
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 120 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.625-6922A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619718 | ||||||
chr5:71619761
|
G | A | 3 | a0001c0001t0010g0257a0001c0001t0010g0337a0001c0002t0003g0254 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-6879G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619761 | ||||||
chr5:71619787
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0225a0001c0003t0003g0194others(2): Show | 6 | HG01167.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-6853C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619787 | ||||||
chr5:71619884
|
G | C | 3 | a0001c0001t0010g0257a0001c0001t0010g0337a0001c0002t0003g0254 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-6756G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619884 | ||||||
chr5:71619915
|
C | T | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.625-6725C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619915 | ||||||
chr5:71619948
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.625-6692G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619948 | ||||||
chr5:71619990
|
C | CA | 22 | a0001c0001t0002g0083a0001c0001t0002g0203a0001c0001t0002g0280others(19): Show | 24 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.625-6637dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71619990 | |||||
chr5:71620028
|
G | A | 1 | a0001c0001t0004g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.625-6612G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620028 | ||||||
chr5:71620099
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.625-6541A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620099 | ||||||
chr5:71620117
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.625-6523A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620117 | ||||||
chr5:71620150
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.625-6490A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620150 | ||||||
chr5:71620165
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.625-6475A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620165 | ||||||
chr5:71620439
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | NA18942.hp2 NA18982.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.625-6201C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620439 | ||||||
chr5:71620445
|
A | G | 15 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0002g0200others(12): Show | 15 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.625-6195A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620445 | ||||||
chr5:71620564
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.625-6076C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620564 | ||||||
chr5:71620779
|
A | G | 13 | a0001c0001t0002g0280a0001c0001t0004g0059a0001c0001t0004g0243others(10): Show | 13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-5861A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620779 | ||||||
chr5:71620807
|
C | T | 2 | a0001c0001t0019g0025a0001c0007t0002g0192 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-5833C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620807 | ||||||
chr5:71621029
|
A | G | 13 | a0001c0001t0002g0280a0001c0001t0004g0059a0001c0001t0004g0243others(10): Show | 13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-5611A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621029 | ||||||
chr5:71621147
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.625-5493C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621147 | ||||||
chr5:71621192
|
GAGAAAGA others(9): Show |
G | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.625-5445_625-5430d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71621192 | |||||
chr5:71621198
|
G | T | 1 | a0001c0001t0003g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.625-5442G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621198 | ||||||
chr5:71621343
|
T | A | 12 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(9): Show | 12 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-5297T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621343 | ||||||
chr5:71621457
|
G | A | 14 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(11): Show | 14 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-5183G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621457 | ||||||
chr5:71621477
|
G | A | 2 | a0001c0001t0019g0025a0001c0007t0002g0192 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-5163G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621477 | ||||||
chr5:71621479
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-5161A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621479 | ||||||
chr5:71621502
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.625-5138G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621502 | ||||||
chr5:71621639
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.625-5001A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621639 | ||||||
chr5:71621895
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.625-4745G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621895 | ||||||
chr5:71622068
|
G | A | 113 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(110): Show | 119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.625-4572G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622068 | ||||||
chr5:71622118
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 141 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.625-4522C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622118 | ||||||
chr5:71622219
|
C | T | 1 | a0001c0010t0004g0249 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.625-4421C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622219 | ||||||
chr5:71622270
|
T | TA | 136 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 140 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.625-4360dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71622270 | |||||
chr5:71622286
|
C | T | 12 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(9): Show | 12 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-4354C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622286 | ||||||
chr5:71622339
|
A | G | 1 | a0001c0001t0002g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.625-4301A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622339 | ||||||
chr5:71622435
|
G | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.625-4205G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622435 | ||||||
chr5:71622449
|
T | C | 10 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-4191T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622449 | ||||||
chr5:71622754
|
C | T | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.625-3886C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622754 | ||||||
chr5:71622832
|
C | T | 1 | a0001c0001t0009g0234 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.625-3808C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622832 | ||||||
chr5:71622903
|
G | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 131 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.625-3737G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622903 | ||||||
chr5:71622992
|
C | T | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-3648C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622992 | ||||||
chr5:71622997
|
C | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG00673.hp2 NA18986.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-3643C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622997 | ||||||
chr5:71623076
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.625-3564A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623076 | ||||||
chr5:71623258
|
T | C | 14 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(11): Show | 14 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-3382T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623258 | ||||||
chr5:71623357
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.625-3283C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623357 | ||||||
chr5:71623459
|
G | A | 10 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-3181G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623459 | ||||||
chr5:71623967
|
C | T | 2 | a0001c0001t0019g0025a0001c0007t0002g0192 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2673C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623967 | ||||||
chr5:71623999
|
G | A | 1 | a0003c0008t0006g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-2641G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623999 | ||||||
chr5:71624181
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.625-2459G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624181 | ||||||
chr5:71624266
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.625-2374A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624266 | ||||||
chr5:71624308
|
A | G | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-2332A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624308 | ||||||
chr5:71624344
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.625-2296C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624344 | ||||||
chr5:71624400
|
C | T | 14 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(11): Show | 14 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-2240C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624400 | ||||||
chr5:71624426
|
G | A | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-2214G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624426 | ||||||
chr5:71624455
|
G | A | 1 | a0001c0001t0002g0301 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.625-2185G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624455 | ||||||
chr5:71624645
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-1995G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624645 | ||||||
chr5:71624663
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 127 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.625-1977T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624663 | ||||||
chr5:71624674
|
G | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.625-1966G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624674 | ||||||
chr5:71624690
|
TTTC | T | 11 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211others(8): Show | 11 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-1947_625-1945d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624690 | |||||
chr5:71624693
|
CT | C | 191 | a0001c0001t0001g0071a0001c0001t0001g0218a0001c0001t0001g0261others(188): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.625-1928delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | |||||
chr5:71624693
|
CTT | C | 6 | a0001c0001t0002g0315a0001c0001t0004g0013a0001c0001t0019g0025others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-1929_625-1928d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | |||||
chr5:71624693
|
CTTT | C | 6 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0002g0093others(3): Show | 6 | HG00733.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-1930_625-1928d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | |||||
chr5:71624693
|
CTTTT | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 121 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.625-1931_625-1928d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | |||||
chr5:71624844
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 141 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.625-1796G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624844 | ||||||
chr5:71625304
|
G | GTCCTTTG others(4): Show |
1 | a0001c0001t0001g0095 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.625-1335_625-1325d others(13): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71625304 | |||||
chr5:71625349
|
G | A | 1 | a0001c0001t0010g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.625-1291G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625349 | ||||||
chr5:71625668
|
A | C | 13 | a0001c0001t0002g0280a0001c0001t0004g0059a0001c0001t0004g0243others(10): Show | 13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-972A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625668 | ||||||
chr5:71625680
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.625-960A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625680 | ||||||
chr5:71625750
|
A | G | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.625-890A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625750 | ||||||
chr5:71625941
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.625-699G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625941 | ||||||
chr5:71625946
|
G | A | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-694G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625946 | ||||||
chr5:71626032
|
C | T | 2 | a0001c0001t0019g0025a0001c0007t0002g0192 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-608C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71626032 | ||||||
chr5:71626301
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(130): Show | 137 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.625-339C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71626301 | ||||||
chr5:71626395
|
C | T | 10 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-245C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71626395 | ||||||
chr5:71626789
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.738+36G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71626789 | ||||||
chr5:71626885
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0151others(35): Show | 38 | HG00140.hp2 HG00597.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.738+132C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71626885 | ||||||
chr5:71626982
|
A | C | 1 | a0001c0002t0003g0012 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.738+229A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71626982 | ||||||
chr5:71627069
|
A | C | 1 | a0001c0001t0002g0137 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.738+316A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627069 | ||||||
chr5:71627141
|
G | T | 131 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(128): Show | 137 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.738+388G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627141 | ||||||
chr5:71627179
|
G | C | 116 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(113): Show | 122 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.738+426G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627179 | ||||||
chr5:71627179
|
G | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.738+426G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627179 | ||||||
chr5:71627336
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.738+583T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627336 | ||||||
chr5:71627531
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.738+778C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627531 | ||||||
chr5:71627600
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.738+847T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627600 | ||||||
chr5:71627628
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.738+875G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627628 | ||||||
chr5:71627801
|
C | A | 1 | a0001c0002t0003g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.738+1048C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627801 | ||||||
chr5:71627825
|
C | CT | 17 | a0001c0001t0002g0232a0001c0001t0002g0259a0001c0001t0003g0212others(14): Show | 17 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.738+1083dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71627825 | |||||
chr5:71628004
|
C | T | 13 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(10): Show | 13 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.738+1251C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628004 | ||||||
chr5:71628124
|
A | G | 1 | a0001c0001t0002g0259 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.738+1371A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628124 | ||||||
chr5:71628140
|
G | T | 124 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(121): Show | 130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.738+1387G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628140 | ||||||
chr5:71628156
|
C | T | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.738+1403C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628156 | ||||||
chr5:71628273
|
C | T | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | NA18957.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.738+1520C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628273 | ||||||
chr5:71628320
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.738+1567G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628320 | ||||||
chr5:71628586
|
G | C | 125 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(122): Show | 131 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.738+1833G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628586 | ||||||
chr5:71628710
|
G | A | 3 | a0001c0001t0007g0196a0001c0001t0007g0253a0001c0001t0015g0019 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.738+1957G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628710 | ||||||
chr5:71628831
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.738+2078A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628831 | ||||||
chr5:71628853
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.738+2100G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628853 | ||||||
chr5:71629043
|
T | C | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.738+2290T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71629043 | ||||||
chr5:71629203
|
C | CA | 134 | a0001c0001t0001g0114a0001c0001t0001g0218a0001c0001t0001g0261others(131): Show | 140 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.738+2462dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629203 | |||||
chr5:71629219
|
A | G | 133 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(130): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.738+2466A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71629219 | ||||||
chr5:71629717
|
A | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-2404A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71629717 | ||||||
chr5:71629735
|
C | CATT | 3 | a0001c0001t0001g0136a0001c0001t0001g0143a0001c0001t0001g0146 | 3 | HG02683.hp2 NA18972.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.739-2360_739-2358d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629735 | |||||
chr5:71629735
|
C | CATTATTA others(5): Show |
1 | a0001c0001t0010g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.739-2369_739-2358d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629735 | |||||
chr5:71629735
|
CATTATT | C | 132 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(129): Show | 138 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.739-2363_739-2358d others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629735 | |||||
chr5:71630290
|
A | G | 6 | a0001c0001t0004g0243a0001c0001t0004g0246a0001c0001t0004g0247others(3): Show | 6 | HG01433.hp2 HG01978.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-1831A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630290 | ||||||
chr5:71630433
|
C | T | 13 | a0001c0001t0002g0280a0001c0001t0004g0059a0001c0001t0004g0243others(10): Show | 13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.739-1688C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630433 | ||||||
chr5:71630549
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 144 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.739-1572A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630549 | ||||||
chr5:71630605
|
T | C | 1 | a0001c0002t0003g0022 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.739-1516T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630605 | ||||||
chr5:71630627
|
G | C | 1 | a0001c0001t0009g0234 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.739-1494G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630627 | ||||||
chr5:71630732
|
A | G | 109 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(106): Show | 115 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.739-1389A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630732 | ||||||
chr5:71630928
|
A | C | 4 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-1193A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630928 | ||||||
chr5:71630991
|
A | G | 1 | a0001c0001t0004g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.739-1130A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630991 | ||||||
chr5:71631171
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.739-950G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631171 | ||||||
chr5:71631349
|
C | T | 1 | a0003c0008t0006g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.739-772C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631349 | ||||||
chr5:71631538
|
C | CT | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 51 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.739-563dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71631538 | |||||
chr5:71631538
|
CTTT | C | 120 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(117): Show | 126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.739-565_739-563del others(3): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71631538 | |||||
chr5:71631615
|
A | G | 4 | a0001c0001t0004g0063a0001c0001t0004g0064a0001c0001t0004g0065others(1): Show | 4 | HG00597.hp2 HG02155.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-506A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631615 | ||||||
chr5:71631676
|
G | T | 1 | a0001c0001t0002g0270 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.739-445G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631676 | ||||||
chr5:71631753
|
C | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 273 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.739-368C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631753 | ||||||
chr5:71631859
|
C | T | 108 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(105): Show | 114 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.739-262C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631859 | ||||||
chr5:71631860
|
G | T | 1 | a0001c0001t0004g0248 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.739-261G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631860 | ||||||
chr5:71631920
|
C | T | 3 | a0001c0001t0002g0232a0001c0001t0019g0025a0001c0007t0002g0192 | 3 | HG00741.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.739-201C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631920 | ||||||
chr5:71632029
|
G | A | 124 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(121): Show | 130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.739-92G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71632029 | ||||||
chr5:71632030
|
G | C | 13 | a0001c0001t0002g0280a0001c0001t0004g0059a0001c0001t0004g0243others(10): Show | 13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.739-91G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71632030 | ||||||
chr5:71632096
|
C | T | 10 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.739-25C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71632096 | ||||||
chr5:71632256
|
C | T | 124 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(121): Show | 130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.803+71C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632256 | ||||||
chr5:71632424
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+239T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632424 | ||||||
chr5:71632474
|
G | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG00673.hp2 NA18986.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+289G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632474 | ||||||
chr5:71632583
|
C | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG00423.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.803+398C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632583 | ||||||
chr5:71632621
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.803+436G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632621 | ||||||
chr5:71632697
|
CA | C | 8 | a0001c0001t0004g0195a0001c0001t0004g0206a0001c0001t0004g0236others(5): Show | 8 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+514delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71632697 | |||||
chr5:71632738
|
G | A | 124 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(121): Show | 130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.803+553G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632738 | ||||||
chr5:71632819
|
C | T | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803+634C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632819 | ||||||
chr5:71632840
|
A | G | 2 | a0001c0001t0010g0257a0001c0001t0010g0337 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.803+655A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632840 | ||||||
chr5:71633091
|
T | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803+906T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633091 | ||||||
chr5:71633091
|
T | TTA | 6 | a0001c0002t0003g0027a0001c0002t0003g0030a0001c0002t0003g0031others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.803+946_803+947dup others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATA | 3 | a0001c0002t0003g0029a0001c0002t0003g0032a0001c0002t0016g0053 | 3 | HG03579.hp1 HG04199.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.803+944_803+947dup others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0003g0212a0001c0002t0003g0036a0001c0002t0003g0042others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+940_803+947dup others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATATAT others(3): Show |
1 | a0001c0002t0003g0056 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803+938_803+947dup others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0007g0253a0001c0002t0003g0035 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.803+936_803+947dup others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATATAT others(7): Show |
6 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0002t0003g0028others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+934_803+947dup others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATATAT others(9): Show |
4 | a0001c0002t0003g0037a0001c0002t0003g0041a0001c0002t0003g0049others(1): Show | 4 | HG02970.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+932_803+947dup others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTATATAT others(11): Show |
1 | a0001c0002t0003g0005 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.803+930_803+947dup others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
T | TTTTATAT others(3): Show |
1 | a0001c0001t0018g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.803+907_803+908ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTA | T | 11 | a0001c0001t0004g0013a0001c0001t0004g0043a0001c0001t0004g0066others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+946_803+947del others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATA | T | 27 | a0001c0001t0001g0071a0001c0001t0002g0061a0001c0001t0002g0062others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.803+944_803+947del others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATA | T | 8 | a0001c0001t0002g0280a0001c0001t0004g0068a0001c0001t0004g0073others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+942_803+947del others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(1): Show |
T | 7 | a0001c0001t0004g0059a0001c0001t0004g0244a0001c0001t0004g0245others(4): Show | 7 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+940_803+947del others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0001g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.803+938_803+947del others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.803+936_803+947del others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(9): Show |
T | 3 | a0001c0001t0014g0256a0001c0002t0002g0255a0001c0003t0003g0226 | 3 | HG00733.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.803+932_803+947del others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(11): Show |
T | 2 | a0001c0001t0002g0222a0001c0001t0002g0292 | 2 | HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.803+930_803+947del others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(13): Show |
T | 103 | a0001c0001t0001g0218a0001c0001t0001g0261a0001c0001t0001g0296others(100): Show | 109 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.803+928_803+947del others(20): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(15): Show |
T | 10 | a0001c0001t0004g0195a0001c0001t0004g0206a0001c0001t0004g0236others(7): Show | 10 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+926_803+947del others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633091
|
TTATATAT others(17): Show |
T | 2 | a0001c0001t0006g0207a0001c0001t0006g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.803+924_803+947del others(24): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | |||||
chr5:71633093
|
A | T | 5 | a0001c0001t0002g0232a0001c0001t0007g0196a0001c0001t0015g0019others(2): Show | 5 | HG00642.hp1 HG00741.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+908A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633093 | ||||||
chr5:71633101
|
A | T | 2 | a0001c0001t0004g0248a0001c0010t0004g0249 | 2 | HG01433.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.803+916A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633101 | ||||||
chr5:71633106
|
TATATATA others(4): Show |
T | 1 | a0001c0002t0003g0012 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.803+922_803+932del others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633106 | ||||||
chr5:71633107
|
ATATATAT others(19): Show |
A | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803+924_803+949del others(26): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633107 | |||||
chr5:71633109
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803+926_803+949del others(24): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633109 | |||||
chr5:71633117
|
A | T | 1 | a0001c0001t0001g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.803+932A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633117 | ||||||
chr5:71633119
|
A | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0215a0001c0002t0003g0012 | 3 | NA18942.hp1 NA18948.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.803+934A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633119 | ||||||
chr5:71633119
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.803+936_803+949del others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633119 | |||||
chr5:71633121
|
A | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0215a0001c0001t0002g0021others(2): Show | 5 | HG01243.hp1 HG03486.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+936A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633121 | ||||||
chr5:71633123
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0214 | 2 | HG01261.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.803+939_803+940ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633123 | |||||
chr5:71633123
|
A | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0126a0001c0001t0001g0173others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+938A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633123 | ||||||
chr5:71633125
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0102 | 2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.803+941_803+942ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633125 | |||||
chr5:71633125
|
A | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0126a0001c0001t0001g0165others(8): Show | 11 | HG01243.hp1 HG01261.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+940A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633125 | ||||||
chr5:71633127
|
A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0152 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.803+945_803+946ins others(15): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0110others(5): Show | 8 | HG01168.hp2 HG02922.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+943_803+944ins others(9): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | ATTTTTTT others(3): Show |
34 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 38 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.803+943_803+944ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0187a0001c0001t0004g0101 | 3 | HG01981.hp1 HG03490.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.803+943_803+944ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0141a0001c0001t0001g0155 | 3 | HG02015.hp2 HG02040.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.803+943_803+944ins others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.803+943_803+944ins others(13): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.803+943_803+944ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | |||||
chr5:71633127
|
A | T | 22 | a0001c0001t0001g0018a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 22 | HG00642.hp2 HG00733.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.803+942A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633127 | ||||||
chr5:71633128
|
T | TTTTTTTT others(3): Show |
2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.803+943_803+944ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633128 | ||||||
chr5:71633129
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0144a0001c0001t0001g0188 | 3 | NA18947.hp2 NA18967.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.803+945_803+946ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | |||||
chr5:71633129
|
A | ATTTTTTT others(4): Show |
5 | a0001c0001t0001g0100a0001c0001t0001g0112a0001c0001t0001g0128others(2): Show | 5 | HG00280.hp1 HG02004.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+945_803+946ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | |||||
chr5:71633129
|
A | ATTTTTTT others(5): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 13 | HG00621.hp1 HG01123.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.803+945_803+946ins others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | |||||
chr5:71633129
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.803+945_803+946ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | |||||
chr5:71633129
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 80 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.803+944A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633129 | ||||||
chr5:71633131
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0168 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(23): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0314 | 2 | HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.803+947_803+948ins others(24): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0006g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.803+947_803+948ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.803+947_803+948ins others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATATTT others(13): Show |
2 | a0001c0001t0001g0127a0001c0001t0001g0318 | 2 | NA19012.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.803+947_803+948ins others(20): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0176 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.803+947_803+948ins others(15): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0117 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.803+951_803+952ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.803+951_803+952ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0151 | 2 | NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.803+951_803+952ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.803+951_803+952ins others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0135 | 3 | NA18984.hp2 NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.803+951_803+952ins others(13): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0154a0001c0001t0001g0179a0001c0001t0004g0105 | 3 | HG00735.hp2 HG01433.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.803+951_803+952ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803+951_803+952ins others(15): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803+951_803+952ins others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | |||||
chr5:71633131
|
A | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 106 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.803+946A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633131 | ||||||
chr5:71633132
|
T | TATATATA others(12): Show |
1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(19): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633132 | ||||||
chr5:71633133
|
T | A | 7 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+948T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633133 | ||||||
chr5:71633134
|
T | A | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.803+949T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633134 | ||||||
chr5:71633135
|
T | A | 2 | a0001c0001t0004g0211a0003c0008t0006g0080 | 2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.803+950T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633135 | ||||||
chr5:71633137
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.803+953_803+954ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633137 | |||||
chr5:71633137
|
A | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0099a0001c0001t0001g0111others(9): Show | 12 | HG00280.hp1 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.803+952A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633137 | ||||||
chr5:71633292
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.803+1107A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633292 | ||||||
chr5:71633306
|
T | C | 1 | a0001c0001t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.803+1121T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633306 | ||||||
chr5:71633326
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+1141G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633326 | ||||||
chr5:71633484
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.803+1299A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633484 | ||||||
chr5:71633551
|
AT | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 129 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.803+1377delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633551 | |||||
chr5:71633683
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.804-1260A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633683 | ||||||
chr5:71633743
|
G | A | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.804-1200G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633743 | ||||||
chr5:71633912
|
A | G | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804-1031A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633912 | ||||||
chr5:71633930
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.804-1013T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633930 | ||||||
chr5:71634219
|
T | C | 1 | a0003c0008t0006g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.804-724T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634219 | ||||||
chr5:71634270
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804-673C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634270 | ||||||
chr5:71634391
|
T | C | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.804-552T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634391 | ||||||
chr5:71634453
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.804-490A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634453 | ||||||
chr5:71634626
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.804-317C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634626 | ||||||
chr5:71634682
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.804-261T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634682 | ||||||
chr5:71635069
|
T | G | 1 | a0001c0001t0004g0068 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.903+27T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 9/16 | chr5 | 71635069 | ||||||
chr5:71635139
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.904-12A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 9/16 | chr5 | 71635139 | ||||||
chr5:71635285
|
T | G | 13 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(10): Show | 13 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.999+39T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635285 | ||||||
chr5:71635407
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.999+161G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635407 | ||||||
chr5:71635436
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 199 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.999+190G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635436 | ||||||
chr5:71635558
|
T | C | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.999+312T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635558 | ||||||
chr5:71635917
|
G | T | 1 | a0001c0002t0002g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.999+671G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635917 | ||||||
chr5:71635946
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.999+700G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635946 | ||||||
chr5:71636040
|
A | G | 4 | a0001c0001t0001g0218a0001c0002t0003g0217a0001c0002t0003g0219others(1): Show | 4 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+794A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636040 | ||||||
chr5:71636056
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.999+810G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636056 | ||||||
chr5:71636129
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0010g0337 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.999+883G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636129 | ||||||
chr5:71636165
|
A | G | 1 | a0001c0001t0004g0250 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.999+919A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636165 | ||||||
chr5:71636175
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.999+929G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636175 | ||||||
chr5:71636343
|
G | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.999+1097G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636343 | ||||||
chr5:71636434
|
G | A | 1 | a0001c0001t0020g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.999+1188G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636434 | ||||||
chr5:71636699
|
C | CAAAT | 3 | a0001c0001t0007g0196a0001c0001t0010g0257a0001c0001t0010g0337 | 3 | HG00642.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.999+1473_999+1476d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71636699 | |||||
chr5:71636821
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.999+1575G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636821 | ||||||
chr5:71636900
|
T | C | 8 | a0001c0001t0004g0195a0001c0001t0004g0206a0001c0001t0004g0237others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+1654T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636900 | ||||||
chr5:71636986
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.999+1740C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636986 | ||||||
chr5:71636987
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.999+1741G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636987 | ||||||
chr5:71637084
|
G | A | 2 | a0001c0002t0003g0224a0001c0002t0003g0254 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.999+1838G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637084 | ||||||
chr5:71637169
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.999+1923T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637169 | ||||||
chr5:71637201
|
A | G | 2 | a0001c0001t0014g0256a0001c0002t0002g0255 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.999+1955A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637201 | ||||||
chr5:71637690
|
A | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 124 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.999+2444A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637690 | ||||||
chr5:71637731
|
T | A | 7 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(4): Show | 7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+2485T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637731 | ||||||
chr5:71637870
|
G | A | 4 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211others(1): Show | 4 | HG02698.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+2624G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637870 | ||||||
chr5:71637928
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.999+2682A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637928 | ||||||
chr5:71637963
|
C | T | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.999+2717C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637963 | ||||||
chr5:71637964
|
G | A | 116 | a0001c0001t0001g0071a0001c0001t0002g0003a0001c0001t0002g0004others(113): Show | 122 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.999+2718G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637964 | ||||||
chr5:71637992
|
A | G | 17 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(14): Show | 17 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.999+2746A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637992 | ||||||
chr5:71638089
|
A | T | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.999+2843A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638089 | ||||||
chr5:71638314
|
A | G | 10 | a0001c0001t0002g0008a0001c0001t0002g0221a0001c0001t0002g0222others(7): Show | 11 | HG02572.hp1 HG02717.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-2689A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638314 | ||||||
chr5:71638324
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(74): Show | 81 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1000-2679T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638324 | ||||||
chr5:71638459
|
C | T | 33 | a0001c0001t0002g0232a0001c0001t0003g0044a0001c0001t0003g0046others(30): Show | 33 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1000-2544C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638459 | ||||||
chr5:71638460
|
G | A | 2 | a0001c0002t0003g0027a0001c0002t0003g0028 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1000-2543G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638460 | ||||||
chr5:71638473
|
C | CAGATCTG others(59): Show |
1 | a0001c0001t0004g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1000-2526_1000-246 others(70): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71638473 | |||||
chr5:71638560
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1000-2443G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638560 | ||||||
chr5:71638696
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1000-2307T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638696 | ||||||
chr5:71638767
|
C | T | 1 | a0001c0002t0003g0081 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1000-2236C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638767 | ||||||
chr5:71638877
|
G | A | 129 | a0001c0001t0001g0071a0001c0001t0002g0003a0001c0001t0002g0004others(126): Show | 135 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1000-2126G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638877 | ||||||
chr5:71639004
|
T | C | 30 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0048others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000-1999T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639004 | ||||||
chr5:71639075
|
C | T | 6 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-1928C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639075 | ||||||
chr5:71639077
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 142 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1000-1926T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639077 | ||||||
chr5:71639192
|
C | T | 1 | a0001c0001t0015g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1000-1811C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639192 | ||||||
chr5:71639382
|
T | C | 3 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1000-1621T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639382 | ||||||
chr5:71639561
|
C | T | 8 | a0001c0002t0003g0002a0001c0002t0003g0023a0001c0002t0003g0051others(5): Show | 10 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-1442C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639561 | ||||||
chr5:71639590
|
T | C | 1 | a0001c0011t0004g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1000-1413T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639590 | ||||||
chr5:71639700
|
T | C | 1 | a0001c0001t0005g0276 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1000-1303T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639700 | ||||||
chr5:71639816
|
A | C | 7 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(4): Show | 7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-1187A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639816 | ||||||
chr5:71640382
|
AT | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 238 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.1000-600delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71640382 | |||||
chr5:71640382
|
ATT | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0112a0001c0001t0001g0135others(58): Show | 61 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1000-601_1000-600d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71640382 | |||||
chr5:71640583
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1000-420G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640583 | ||||||
chr5:71640704
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0019g0025a0001c0007t0002g0192 | 3 | HG00741.hp1 HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1000-299G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640704 | ||||||
chr5:71640753
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1000-250G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640753 | ||||||
chr5:71640766
|
T | G | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1000-237T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640766 | ||||||
chr5:71640816
|
C | G | 122 | a0001c0001t0001g0071a0001c0001t0002g0003a0001c0001t0002g0004others(119): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1000-187C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640816 | ||||||
chr5:71640852
|
T | C | 1 | a0001c0001t0004g0101 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1000-151T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640852 | ||||||
chr5:71641104
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1072+29A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641104 | ||||||
chr5:71641133
|
T | G | 7 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(4): Show | 7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1072+58T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641133 | ||||||
chr5:71641282
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1072+207G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641282 | ||||||
chr5:71641378
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1072+303C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641378 | ||||||
chr5:71641625
|
A | G | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1072+550A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641625 | ||||||
chr5:71641697
|
A | G | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1072+622A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641697 | ||||||
chr5:71641815
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0119others(2): Show | 5 | HG02083.hp1 NA18957.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072+740A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641815 | ||||||
chr5:71642137
|
G | A | 26 | a0001c0001t0003g0212a0001c0001t0004g0209a0001c0001t0004g0210others(23): Show | 26 | HG00733.hp2 HG01167.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1072+1062G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642137 | ||||||
chr5:71642265
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 237 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1072+1190C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642265 | ||||||
chr5:71642270
|
A | T | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1072+1195A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642270 | ||||||
chr5:71642318
|
G | T | 1 | a0001c0002t0002g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1072+1243G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642318 | ||||||
chr5:71642440
|
G | A | 2 | a0001c0001t0002g0279a0001c0001t0002g0289 | 2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1072+1365G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642440 | ||||||
chr5:71642550
|
A | T | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1073-1269A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642550 | ||||||
chr5:71642559
|
T | C | 6 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073-1260T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642559 | ||||||
chr5:71642649
|
C | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1073-1170C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642649 | ||||||
chr5:71642857
|
A | G | 2 | a0001c0001t0004g0246a0001c0001t0004g0247 | 2 | HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1073-962A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642857 | ||||||
chr5:71642927
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1073-892C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642927 | ||||||
chr5:71642954
|
G | C | 91 | a0001c0001t0001g0071a0001c0001t0002g0003a0001c0001t0002g0004others(88): Show | 96 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1073-865G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642954 | ||||||
chr5:71642963
|
A | G | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1073-856A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642963 | ||||||
chr5:71642981
|
C | T | 30 | a0001c0001t0003g0044a0001c0001t0003g0046a0001c0001t0003g0048others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1073-838C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642981 | ||||||
chr5:71643055
|
A | G | 1 | a0001c0001t0004g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1073-764A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643055 | ||||||
chr5:71643125
|
A | G | 7 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(4): Show | 7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073-694A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643125 | ||||||
chr5:71643202
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1073-617C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643202 | ||||||
chr5:71643264
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1073-555C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643264 | ||||||
chr5:71643303
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 231 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1073-516T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643303 | ||||||
chr5:71643360
|
C | G | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1073-459C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643360 | ||||||
chr5:71643412
|
A | G | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1073-407A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643412 | ||||||
chr5:71643610
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 264 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1073-209G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643610 | ||||||
chr5:71643645
|
A | G | 1 | a0001c0001t0017g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073-174A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643645 | ||||||
chr5:71643690
|
A | T | 1 | a0001c0001t0009g0234 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1073-129A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643690 | ||||||
chr5:71643721
|
G | C | 1 | a0001c0001t0018g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1073-98G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643721 | ||||||
chr5:71643741
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1073-78G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643741 | ||||||
chr5:71643958
|
A | G | 3 | a0001c0002t0003g0055a0001c0002t0003g0056a0001c0002t0003g0081 | 3 | NA18966.hp2 NA19081.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1149+63A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71643958 | ||||||
chr5:71644032
|
C | CGT | 3 | a0001c0001t0004g0105a0001c0001t0008g0251a0001c0001t0008g0252 | 3 | HG01433.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1149+137_1149+138i others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644032 | ||||||
chr5:71644033
|
A | ATG | 26 | a0001c0001t0001g0020a0001c0001t0001g0106a0001c0001t0001g0112others(23): Show | 26 | HG00280.hp1 HG00438.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1149+175_1149+176d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTG | 144 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 150 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149+173_1149+176d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTGTG | 53 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0094others(50): Show | 55 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1149+171_1149+176d others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTGTGT others(1): Show |
13 | a0001c0001t0001g0136a0001c0001t0001g0173a0001c0001t0002g0009others(10): Show | 14 | HG00735.hp1 HG02155.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1149+169_1149+176d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTGTGT others(3): Show |
16 | a0001c0001t0002g0021a0001c0001t0004g0013a0001c0001t0004g0033others(13): Show | 16 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1149+167_1149+176d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0004g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1149+165_1149+176d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0004g0066 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1149+163_1149+176d others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0004g0068 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1149+161_1149+176d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644033
|
A | G | 11 | a0001c0001t0004g0105a0001c0001t0006g0024a0001c0001t0006g0207others(8): Show | 11 | HG00733.hp2 HG00741.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1149+138A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644033 | ||||||
chr5:71644033
|
ATG | A | 4 | a0001c0001t0003g0212a0001c0001t0010g0257a0001c0001t0010g0337others(1): Show | 4 | HG01192.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+175_1149+176d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | |||||
chr5:71644060
|
TGTGTGTG others(7): Show |
T | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1149+167_1149+180d others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644060 | |||||
chr5:71644062
|
TGTGTGTG others(5): Show |
T | 11 | a0001c0001t0002g0008a0001c0001t0002g0221a0001c0001t0002g0222others(8): Show | 12 | HG02257.hp1 HG02572.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1149+169_1149+180d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644062 | |||||
chr5:71644070
|
T | C | 2 | a0001c0002t0003g0049a0001c0002t0024g0026 | 2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1149+175T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644070 | ||||||
chr5:71644070
|
TGC | T | 5 | a0001c0001t0002g0061a0001c0001t0002g0283a0001c0001t0004g0239others(2): Show | 5 | HG01255.hp1 HG02738.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+181_1149+182d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644070 | |||||
chr5:71644070
|
TGCGC | T | 6 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+179_1149+182d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644070 | |||||
chr5:71644072
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1149+177C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644072 | ||||||
chr5:71644074
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 221 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1149+179C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644074 | ||||||
chr5:71644466
|
A | G | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1149+571A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644466 | ||||||
chr5:71644747
|
T | C | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1149+852T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644747 | ||||||
chr5:71644976
|
T | A | 6 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+1081T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644976 | ||||||
chr5:71645002
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0168 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1149+1107G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645002 | ||||||
chr5:71645210
|
G | A | 1 | a0001c0006t0002g0274 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1150-1001G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645210 | ||||||
chr5:71645254
|
C | T | 10 | a0001c0001t0004g0059a0001c0001t0004g0243a0001c0001t0004g0244others(7): Show | 10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-957C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645254 | ||||||
chr5:71645267
|
G | A | 37 | a0001c0001t0002g0093a0001c0001t0002g0232a0001c0001t0003g0044others(34): Show | 37 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1150-944G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645267 | ||||||
chr5:71645458
|
T | G | 1 | a0001c0001t0001g0216 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1150-753T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645458 | ||||||
chr5:71645555
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1150-656A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645555 | ||||||
chr5:71645685
|
C | T | 1 | a0001c0001t0002g0003 | 3 | HG00280.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1150-526C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645685 | ||||||
chr5:71646064
|
T | TA | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1150-135dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71646064 | |||||
chr5:71646106
|
G | T | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1150-105G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71646106 | ||||||
chr5:71646135
|
T | G | 1 | a0001c0002t0003g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150-76T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71646135 | ||||||
chr5:71646338
|
C | T | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1216+61C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646338 | ||||||
chr5:71646440
|
A | G | 3 | a0001c0001t0007g0196a0001c0001t0007g0253a0001c0001t0015g0019 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1216+163A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646440 | ||||||
chr5:71646509
|
G | A | 37 | a0001c0001t0002g0093a0001c0001t0002g0232a0001c0001t0003g0044others(34): Show | 37 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1216+232G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646509 | ||||||
chr5:71646611
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1216+334C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646611 | ||||||
chr5:71646700
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1216+423A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646700 | ||||||
chr5:71646742
|
T | G | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1216+465T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646742 | ||||||
chr5:71646777
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1216+500A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646777 | ||||||
chr5:71646858
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0003g0048 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1216+581G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646858 | ||||||
chr5:71646928
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1216+651T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646928 | ||||||
chr5:71647246
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1216+969G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647246 | ||||||
chr5:71647257
|
G | A | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1216+980G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647257 | ||||||
chr5:71647354
|
A | G | 25 | a0001c0001t0004g0013a0001c0001t0004g0033a0001c0001t0004g0043others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1216+1077A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647354 | ||||||
chr5:71647400
|
A | T | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1216+1123A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647400 | ||||||
chr5:71647411
|
T | C | 1 | a0001c0001t0002g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1216+1134T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647411 | ||||||
chr5:71647660
|
G | T | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1216+1383G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647660 | ||||||
chr5:71647920
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1217-1177C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647920 | ||||||
chr5:71647978
|
T | G | 2 | a0001c0001t0007g0196a0001c0001t0007g0253 | 2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1217-1119T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647978 | ||||||
chr5:71648292
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1217-805G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648292 | ||||||
chr5:71648431
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1217-666T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648431 | ||||||
chr5:71648794
|
G | A | 6 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1217-303G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648794 | ||||||
chr5:71648949
|
T | C | 3 | a0001c0001t0003g0212a0001c0001t0010g0257a0001c0001t0010g0337 | 3 | HG02451.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1217-148T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648949 | ||||||
chr5:71648952
|
C | T | 4 | a0001c0001t0006g0024a0001c0001t0006g0207a0001c0001t0006g0208others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217-145C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648952 | ||||||
chr5:71649018
|
C | T | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1217-79C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71649018 | ||||||
chr5:71649090
|
C | G | 1 | a0001c0002t0024g0026 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.1217-7C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71649090 | ||||||
chr5:71649344
|
A | C | 1 | a0001c0001t0002g0230 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1373+91A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649344 | ||||||
chr5:71649356
|
G | C | 1 | a0001c0001t0002g0291 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1373+103G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649356 | ||||||
chr5:71649384
|
A | G | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1373+131A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649384 | ||||||
chr5:71649626
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1373+373C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649626 | ||||||
chr5:71649636
|
G | A | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1373+383G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649636 | ||||||
chr5:71649814
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1374-255C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649814 | ||||||
chr5:71650024
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1374-45T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71650024 | ||||||
chr5:71650286
|
G | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 122 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1488+103G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650286 | ||||||
chr5:71650296
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 119 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1488+113G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650296 | ||||||
chr5:71650444
|
C | T | 1 | a0001c0001t0004g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1488+261C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650444 | ||||||
chr5:71650495
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1488+312C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650495 | ||||||
chr5:71650496
|
G | T | 3 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1488+313G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650496 | ||||||
chr5:71650503
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1488+320C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650503 | ||||||
chr5:71650641
|
T | TTTTA | 3 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1488+478_1488+481d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr5 | 71650641 | |||||
chr5:71650680
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1488+497G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650680 | ||||||
chr5:71650712
|
G | A | 48 | a0001c0001t0002g0093a0001c0001t0002g0232a0001c0001t0002g0280others(45): Show | 48 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1488+529G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650712 | ||||||
chr5:71650718
|
G | A | 2 | a0001c0003t0003g0194a0001c0003t0003g0226 | 2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1488+535G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650718 | ||||||
chr5:71650758
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1488+575T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650758 | ||||||
chr5:71650809
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1488+626T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650809 | ||||||
chr5:71650885
|
G | T | 1 | a0001c0001t0008g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1488+702G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650885 | ||||||
chr5:71651046
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(273): Show | 286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1488+863T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651046 | ||||||
chr5:71651047
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1488+864G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651047 | ||||||
chr5:71651323
|
G | GA | 3 | a0001c0001t0007g0196a0001c0001t0007g0253a0001c0001t0015g0019 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1488+1143dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr5 | 71651323 | |||||
chr5:71651423
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1488+1240G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651423 | ||||||
chr5:71651459
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1489-1210T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651459 | ||||||
chr5:71651474
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1489-1195T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651474 | ||||||
chr5:71651690
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1489-979T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651690 | ||||||
chr5:71651723
|
T | C | 2 | a0001c0001t0009g0234a0001c0001t0009g0235 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1489-946T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651723 | ||||||
chr5:71651837
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1489-832C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651837 | ||||||
chr5:71652194
|
T | C | 1 | a0001c0007t0002g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1489-475T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71652194 | ||||||
chr5:71652436
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1489-233C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71652436 | ||||||
chr5:71652558
|
T | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1489-111T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71652558 | ||||||
chr5:71652827
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1574+73G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71652827 | ||||||
chr5:71652991
|
G | A | 90 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0009others(87): Show | 95 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1574+237G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71652991 | ||||||
chr5:71653052
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1574+298G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653052 | ||||||
chr5:71653218
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1574+464C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653218 | ||||||
chr5:71653282
|
C | A | 1 | a0001c0001t0007g0196 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1574+528C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653282 | ||||||
chr5:71653383
|
T | TC | 3 | a0001c0001t0003g0212a0001c0001t0010g0257a0001c0001t0010g0337 | 3 | HG02451.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1574+630dupC | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71653383 | |||||
chr5:71653418
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A | AGACTAAT others(51): Show |
1 | a0001c0001t0002g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1574+665_1574+722d others(60): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71653418 | |||||
chr5:71653593
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T | A | 4 | a0001c0001t0002g0061a0001c0001t0002g0072a0001c0001t0002g0083others(1): Show | 4 | NA18943.hp2 NA18948.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1574+839T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653593 | ||||||
chr5:71653628
|
T | C | 3 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1574+874T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653628 | ||||||
chr5:71653651
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A | T | 1 | a0001c0001t0002g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1574+897A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653651 | ||||||
chr5:71653678
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G | A | 1 | a0001c0001t0004g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1574+924G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653678 | ||||||
chr5:71653823
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C | T | 1 | a0001c0001t0001g0144 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1574+1069C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653823 | ||||||
chr5:71653850
|
CA | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1574+1113delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71653850 | |||||
chr5:71654086
|
C | T | 1 | a0003c0008t0006g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1574+1332C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654086 | ||||||
chr5:71654091
|
G | A | 3 | a0001c0001t0007g0196a0001c0001t0007g0253a0001c0001t0015g0019 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1574+1337G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654091 | ||||||
chr5:71654466
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T | A | 8 | a0001c0001t0004g0195a0001c0001t0004g0206a0001c0001t0004g0236others(5): Show | 8 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1574+1712T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654466 | ||||||
chr5:71654479
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A | G | 1 | a0001c0001t0004g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1574+1725A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654479 | ||||||
chr5:71654557
|
G | T | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1574+1803G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654557 | ||||||
chr5:71654763
|
G | A | 3 | a0001c0001t0007g0196a0001c0001t0007g0253a0001c0001t0015g0019 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1575-1980G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654763 | ||||||
chr5:71654836
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1575-1907G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654836 | ||||||
chr5:71654837
|
A | AT | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0185others(3): Show | 6 | HG00673.hp2 HG01978.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575-1888dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71654837 | |||||
chr5:71654911
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(282): Show | 295 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1575-1832T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654911 | ||||||
chr5:71654959
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1575-1784C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654959 | ||||||
chr5:71654992
|
G | A | 1 | a0001c0001t0014g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1575-1751G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654992 | ||||||
chr5:71655080
|
C | T | 3 | a0001c0001t0003g0212a0001c0001t0010g0257a0001c0001t0010g0337 | 3 | HG02451.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1575-1663C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655080 | ||||||
chr5:71655105
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1575-1638A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655105 | ||||||
chr5:71655114
|
A | G | 1 | a0001c0001t0019g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1575-1629A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655114 | ||||||
chr5:71655220
|
C | A | 1 | a0001c0001t0002g0313 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1575-1523C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655220 | ||||||
chr5:71655405
|
T | C | 3 | a0001c0001t0002g0232a0001c0001t0019g0025a0001c0007t0002g0192 | 3 | HG00741.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1575-1338T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655405 | ||||||
chr5:71655406
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1575-1337C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655406 | ||||||
chr5:71655471
|
G | T | 3 | a0001c0001t0007g0196a0001c0001t0007g0253a0001c0001t0015g0019 | 3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1575-1272G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655471 | ||||||
chr5:71655826
|
A | G | 19 | a0001c0001t0002g0280a0001c0001t0004g0059a0001c0001t0004g0195others(16): Show | 19 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1575-917A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655826 | ||||||
chr5:71656104
|
G | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1575-639G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656104 | ||||||
chr5:71656154
|
G | T | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1575-589G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656154 | ||||||
chr5:71656356
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1575-387G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656356 | ||||||
chr5:71656543
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1575-200T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656543 | ||||||
chr5:71656590
|
G | A | 2 | a0001c0001t0008g0251a0001c0001t0008g0252 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1575-153G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656590 | ||||||
chr5:71656639
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1575-104A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656639 | ||||||
chr5:71656679
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 251 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1575-64A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656679 |