geneid | 4248 |
---|---|
ensemblid | ENSG00000128268.12 |
hgncid | 7046 |
symbol | MGAT3 |
name | beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase |
refseq_nuc | NM_002409.5 |
refseq_prot | NP_002400.3 |
ensembl_nuc | ENST00000341184.7 |
ensembl_prot | ENSP00000345270.6 |
mane_status | MANE Select |
chr | chr22 |
start | 39457012 |
end | 39492194 |
strand | + |
ver | v1.2 |
region | chr22:39457012-39492194 |
region5000 | chr22:39452012-39497194 |
regionname0 | MGAT3_chr22_39457012_39492194 |
regionname5000 | MGAT3_chr22_39452012_39497194 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 533 | 303 | 95 | 74 | 70 | 18 | 44 | 40 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0002 | 0/0 | 533 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0003 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1602 | 245 | 72 | 71 | 45 | 15 | 40 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0002 | 0/0 | 1602 | 46 | 20 | 3 | 20 | 0 | 3 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0003 | 0/0 | 1602 | 4 | 0 | 0 | 1 | 2 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0004 | 0/0 | 1602 | 4 | 0 | 0 | 4 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0005 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0006 | 0/0 | 1602 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0007 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0008 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
c0009 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3792 | 148 | 28 | 47 | 36 | 13 | 23 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0002 | 0/0 | 3792 | 38 | 9 | 4 | 19 | 2 | 4 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0003 | 0/0 | 3792 | 23 | 11 | 3 | 1 | 0 | 8 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0004 | 1/0 | 3792 | 21 | 2 | 8 | 3 | 1 | 6 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0005 | 0/0 | 3792 | 12 | 12 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0006 | 0/0 | 3792 | 9 | 7 | 1 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0007 | 0/0 | 3791 | 7 | 7 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0008 | 0/0 | 3792 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0009 | 0/0 | 3792 | 4 | 0 | 0 | 4 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0010 | 0/0 | 3792 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0011 | 0/0 | 3795 | 3 | 1 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0012 | 0/0 | 3792 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0013 | 0/0 | 3793 | 2 | 0 | 1 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0014 | 0/0 | 3792 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0015 | 0/0 | 3792 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0016 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0017 | 0/0 | 3793 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0018 | 0/0 | 3792 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0019 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0020 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0021 | 0/0 | 3791 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0022 | 0/0 | 3792 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0023 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0024 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0025 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0026 | 0/0 | 3793 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0027 | 0/0 | 3796 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0028 | 0/0 | 3792 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0029 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0030 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0031 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0032 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0033 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0034 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0035 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0036 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0037 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0038 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0039 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
t0040 | 0/0 | 3792 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0002 | 0/0 | 6 | 0 | 0 | 0 | 4 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0003 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0009 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1602 | 245 | 72 | 71 | 45 | 15 | 40 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002 | 0/0 | 1602 | 46 | 20 | 3 | 20 | 0 | 3 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0003 | 0/0 | 1602 | 4 | 0 | 0 | 1 | 2 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0004 | 0/0 | 1602 | 4 | 0 | 0 | 4 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0005 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0007 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0008 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0002c0006 | 0/0 | 1602 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0003c0009 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5393 | 145 | 28 | 47 | 34 | 12 | 23 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0002 | 0/0 | 5393 | 3 | 1 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0003 | 0/0 | 5393 | 22 | 10 | 3 | 1 | 0 | 8 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0004 | 1/0 | 5393 | 21 | 2 | 8 | 3 | 1 | 6 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0005 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0006 | 0/0 | 5393 | 9 | 7 | 1 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0007 | 0/0 | 5392 | 7 | 7 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0008 | 0/0 | 5393 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0010 | 0/0 | 5393 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0011 | 0/0 | 5396 | 3 | 1 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0012 | 0/0 | 5393 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0013 | 0/0 | 5394 | 2 | 0 | 1 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0014 | 0/0 | 5393 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0017 | 0/0 | 5394 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0019 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0020 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0021 | 0/0 | 5392 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0022 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0023 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0024 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0026 | 0/0 | 5394 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0027 | 0/0 | 5397 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0028 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0029 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0030 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0031 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0032 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0033 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0034 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0035 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0036 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0038 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0039 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0001t0040 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002t0002 | 0/0 | 5393 | 31 | 8 | 2 | 18 | 0 | 3 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002t0005 | 0/0 | 5393 | 11 | 11 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002t0016 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002t0018 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002t0025 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0002t0037 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0003t0002 | 0/0 | 5393 | 4 | 0 | 0 | 1 | 2 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0004t0009 | 0/0 | 5393 | 4 | 0 | 0 | 4 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0005t0015 | 0/0 | 5393 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0007t0008 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0001c0008t0001 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0002c0006t0001 | 0/0 | 5393 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
a0003c0009t0003 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | copy fasta | chr22 | 39452012 | 39497194 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 0 | 3 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0009 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0007g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0011g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0012g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0012g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0017g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0020g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0021g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0022g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0023g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0024g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0026g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0027g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0028g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0029g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0030g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0031g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0032g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0033g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0034g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0035g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0036g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0038g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0039g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0001t0040g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0018g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0025g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0002t0037g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0004t0009g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0004t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0005t0015g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0007t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0002c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0002c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
a0003c0009t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00099 | hp2 | a0001 | c0008 | t0001 | g0002 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0228 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00280 | hp1 | a0001 | c0001 | t0024 | g0106 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00423 | hp1 | a0001 | c0001 | t0026 | g0038 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00609 | hp2 | a0001 | c0001 | t0035 | g0041 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0073 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00639 | hp2 | a0001 | c0001 | t0012 | g0229 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0224 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00642 | hp2 | a0001 | c0001 | t0013 | g0028 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01081 | hp1 | a0001 | c0001 | t0040 | g0121 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01099 | hp2 | a0001 | c0001 | t0017 | g0003 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0125 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01167 | hp1 | a0001 | c0002 | t0018 | g0235 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01175 | hp1 | a0001 | c0001 | t0021 | g0213 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01243 | hp1 | a0001 | c0001 | t0022 | g0216 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01496 | hp2 | a0001 | c0001 | t0012 | g0226 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0207 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01517 | hp1 | a0001 | c0003 | t0002 | g0206 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01934 | hp1 | a0001 | c0001 | t0011 | g0074 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01943 | hp1 | a0001 | c0001 | t0028 | g0203 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02129 | hp2 | a0001 | c0001 | t0033 | g0190 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0208 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02258 | hp2 | a0003 | c0009 | t0003 | g0075 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02451 | hp2 | a0001 | c0002 | t0005 | g0103 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02647 | hp1 | a0001 | c0001 | t0020 | g0234 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02647 | hp2 | a0001 | c0001 | t0036 | g0087 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02698 | hp2 | a0001 | c0001 | t0030 | g0194 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02717 | hp1 | a0001 | c0002 | t0005 | g0114 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0098 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0174 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02886 | hp1 | a0001 | c0002 | t0005 | g0113 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02895 | hp1 | a0001 | c0001 | t0014 | g0086 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02922 | hp2 | a0001 | c0001 | t0010 | g0079 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0015 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02965 | hp2 | a0001 | c0001 | t0038 | g0051 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02976 | hp1 | a0001 | c0001 | t0029 | g0063 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03041 | hp2 | a0001 | c0007 | t0008 | g0123 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03098 | hp1 | a0001 | c0002 | t0005 | g0126 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0243 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0150 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0236 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03486 | hp1 | a0001 | c0002 | t0016 | g0210 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0139 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03516 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03516 | hp2 | a0001 | c0001 | t0027 | g0030 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03579 | hp2 | a0001 | c0002 | t0005 | g0015 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0225 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03831 | hp1 | a0001 | c0001 | t0023 | g0176 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03831 | hp2 | a0001 | c0001 | t0039 | g0187 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0170 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | CHB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18906 | hp1 | a0001 | c0005 | t0015 | g0011 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18952 | hp2 | a0001 | c0001 | t0031 | g0171 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18964 | hp2 | a0001 | c0004 | t0009 | g0008 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA18994 | hp2 | a0001 | c0002 | t0025 | g0100 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19007 | hp1 | a0002 | c0006 | t0001 | g0148 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19007 | hp2 | a0001 | c0004 | t0009 | g0008 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19009 | hp1 | a0001 | c0004 | t0009 | g0172 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19009 | hp2 | a0001 | c0002 | t0037 | g0181 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19011 | hp2 | a0001 | c0004 | t0009 | g0008 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19043 | hp2 | a0001 | c0001 | t0019 | g0237 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19056 | hp2 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19075 | hp2 | a0001 | c0001 | t0034 | g0133 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19080 | hp2 | a0001 | c0001 | t0032 | g0143 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19090 | hp1 | a0001 | c0001 | t0013 | g0183 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19090 | hp2 | a0002 | c0006 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0030 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20129 | hp1 | a0001 | c0005 | t0015 | g0011 | AFR | ASW | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | ASW | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0223 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | GIH | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | GIH | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0101 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02559 | hp1 | a0001 | c0002 | t0005 | g0209 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG02559 | hp2 | a0001 | c0002 | t0005 | g0239 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0238 | REF | REF | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39487544
|
G | T | 1 | a0003 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.197G>T | p.Gly66Val | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 744/5394 | 197/1602 | 66/533 | chr22 | 39487544 | ||
chr22:39487600
|
C | T | 1 | a0002 | 2 | NA19007.hp1 NA19090.hp2 |
missense_variant | MODERATE | c.253C>T | p.Pro85Ser | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 800/5394 | 253/1602 | 85/533 | chr22 | 39487600 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39487599
|
G | T | 1 | a0002c0006 | 2 | NA19007.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.252G>T | p.Leu84Leu | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 799/5394 | 252/1602 | 84/533 | chr22 | 39487599 | ||
chr22:39487731
|
G | C | 2 | a0001c0002a0001c0003 | 50 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
synonymous_variant | LOW | c.384G>C | p.Pro128Pro | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 931/5394 | 384/1602 | 128/533 | chr22 | 39487731 | ||
chr22:39488274
|
C | T | 1 | a0001c0004 | 4 | NA18964.hp2 NA19007.hp2 NA19009.hp1 others(1): Show |
synonymous_variant | LOW | c.927C>T | p.Pro309Pro | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1474/5394 | 927/1602 | 309/533 | chr22 | 39488274 | ||
chr22:39488352
|
C | G | 1 | a0001c0008 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1005C>G | p.Gly335Gly | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1552/5394 | 1005/1602 | 335/533 | chr22 | 39488352 | ||
chr22:39488388
|
G | A | 1 | a0001c0005 | 2 | NA18906.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.1041G>A | p.Ser347Ser | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1588/5394 | 1041/1602 | 347/533 | chr22 | 39488388 | ||
chr22:39488436
|
A | G | 1 | a0001c0007 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1089A>G | p.Ser363Ser | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1636/5394 | 1089/1602 | 363/533 | chr22 | 39488436 | ||
chr22:39488937
|
G | A | 1 | a0001c0003 | 4 | HG01515.hp1 HG01517.hp1 HG03927.hp1 others(1): Show |
synonymous_variant | LOW | c.1590G>A | p.Glu530Glu | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2137/5394 | 1590/1602 | 530/533 | chr22 | 39488937 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39457185
|
C | A | 1 | a0001c0002t0016 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-374C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 30163 | chr22 | 39457185 | |||||
chr22:39457244
|
C | G | 1 | a0001c0001t0040 | 1 | HG01081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-315C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 30104 | chr22 | 39457244 | |||||
chr22:39457253
|
C | G | 1 | a0001c0001t0039 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-306C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 30095 | chr22 | 39457253 | |||||
chr22:39457308
|
C | T | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-251C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | chr22 | 39457308 | ||||||
chr22:39457362
|
T | G | 1 | a0001c0001t0023 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-197T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 29986 | chr22 | 39457362 | |||||
chr22:39457411
|
G | C | 1 | a0001c0001t0024 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 29937 | chr22 | 39457411 | |||||
chr22:39457458
|
G | A | 2 | a0001c0001t0024a0001c0002t0025 | 2 | HG00280.hp1 NA18994.hp2 |
5_prime_UTR_variant | MODIFIER | c.-101G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 29890 | chr22 | 39457458 | |||||
chr22:39457525
|
C | T | 1 | a0001c0001t0022 | 1 | HG01243.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | chr22 | 39457525 | ||||||
chr22:39488982
|
C | CG | 4 | a0001c0001t0013a0001c0001t0017a0001c0001t0026others(1): Show | 5 | HG00423.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*38dupG | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 39 | INFO_REALIGN_3_PRIME | chr22 | 39488982 | ||||
chr22:39489166
|
G | T | 3 | a0001c0001t0011a0001c0001t0027a0001c0001t0038 | 5 | HG00639.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*217G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 217 | chr22 | 39489166 | |||||
chr22:39489182
|
C | T | 1 | a0001c0002t0037 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*233C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 233 | chr22 | 39489182 | |||||
chr22:39489250
|
C | T | 3 | a0001c0001t0011a0001c0001t0027a0001c0001t0038 | 5 | HG00639.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*301C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 301 | chr22 | 39489250 | |||||
chr22:39489552
|
C | A | 1 | a0001c0001t0028 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 603 | chr22 | 39489552 | |||||
chr22:39489645
|
G | A | 1 | a0001c0001t0029 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*696G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 696 | chr22 | 39489645 | |||||
chr22:39489719
|
TG | T | 2 | a0001c0001t0007a0001c0001t0021 | 8 | HG01175.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*771delG | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 771 | chr22 | 39489719 | |||||
chr22:39490052
|
G | A | 2 | a0001c0001t0030a0001c0001t0040 | 2 | HG01081.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1103G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1103 | chr22 | 39490052 | |||||
chr22:39490212
|
C | G | 5 | a0001c0001t0003a0001c0001t0006a0001c0001t0022others(2): Show | 34 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1263C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1263 | chr22 | 39490212 | |||||
chr22:39490219
|
C | G | 2 | a0001c0001t0020a0001c0001t0036 | 2 | HG02647.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1270 | chr22 | 39490219 | |||||
chr22:39490226
|
G | GCTT | 2 | a0001c0001t0011a0001c0001t0027 | 4 | HG00639.hp1 HG01934.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1278_*1279insTTC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1279 | INFO_REALIGN_3_PRIME | chr22 | 39490226 | ||||
chr22:39490228
|
A | C | 2 | a0001c0001t0011a0001c0001t0027 | 4 | HG00639.hp1 HG01934.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1279A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1279 | chr22 | 39490228 | |||||
chr22:39490364
|
T | C | 1 | a0001c0001t0038 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1415T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1415 | chr22 | 39490364 | |||||
chr22:39490510
|
G | A | 1 | a0001c0001t0031 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1561 | chr22 | 39490510 | |||||
chr22:39490528
|
C | G | 4 | a0001c0001t0005a0001c0001t0019a0001c0002t0005others(1): Show | 14 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1579C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1579 | chr22 | 39490528 | |||||
chr22:39490550
|
G | A | 1 | a0001c0004t0009 | 4 | NA18964.hp2 NA19007.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1601G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1601 | chr22 | 39490550 | |||||
chr22:39490633
|
C | T | 1 | a0001c0001t0035 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1684 | chr22 | 39490633 | |||||
chr22:39490679
|
G | A | 1 | a0001c0001t0032 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1730 | chr22 | 39490679 | |||||
chr22:39490745
|
T | G | 1 | a0001c0001t0033 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1796 | chr22 | 39490745 | |||||
chr22:39491062
|
C | A | 1 | a0001c0001t0034 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2113C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2113 | chr22 | 39491062 | |||||
chr22:39491207
|
C | T | 4 | a0001c0001t0007a0001c0001t0012a0001c0001t0021others(1): Show | 12 | HG00639.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2258C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2258 | chr22 | 39491207 | |||||
chr22:39491230
|
G | A | 1 | a0001c0001t0010 | 3 | HG02818.hp1 HG02922.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2281G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2281 | chr22 | 39491230 | |||||
chr22:39491537
|
C | G | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0011others(9): Show | 29 | HG00639.hp1 HG00639.hp2 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2588C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2588 | chr22 | 39491537 | |||||
chr22:39491550
|
G | C | 4 | a0001c0001t0005a0001c0001t0019a0001c0002t0005others(1): Show | 14 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2601G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2601 | chr22 | 39491550 | |||||
chr22:39491681
|
A | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(24): Show | 117 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2732A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2732 | chr22 | 39491681 | |||||
chr22:39491891
|
G | T | 1 | a0001c0001t0014 | 2 | HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2942G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2942 | chr22 | 39491891 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39457587
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0242others(4): Show | 10 | HG02280.hp2 HG02572.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+30C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457587 | ||||||
chr22:39457700
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-2+143C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457700 | ||||||
chr22:39457735
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-2+178G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457735 | ||||||
chr22:39457736
|
G | C | 32 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0049others(29): Show | 38 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-2+179G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457736 | ||||||
chr22:39458099
|
AGGGCCCC others(19): Show |
A | 1 | a0001c0001t0004g0240 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-2+554_-2+579delCA others(24): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39458099 | |||||
chr22:39458350
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-2+793A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458350 | ||||||
chr22:39458362
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+805G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458362 | ||||||
chr22:39458363
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2+806C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458363 | ||||||
chr22:39458416
|
C | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-2+859C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458416 | ||||||
chr22:39458545
|
G | C | 8 | a0001c0001t0006g0031a0001c0001t0006g0214a0001c0001t0006g0215others(5): Show | 9 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+988G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458545 | ||||||
chr22:39458817
|
A | G | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+1260A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458817 | ||||||
chr22:39458979
|
C | T | 2 | a0001c0001t0011g0030a0001c0001t0027g0030 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+1422C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458979 | ||||||
chr22:39459072
|
CT | C | 30 | a0001c0001t0001g0072a0001c0001t0001g0245a0001c0001t0001g0246others(27): Show | 35 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-2+1534delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459072 | |||||
chr22:39459072
|
CTTTTTT | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-2+1529_-2+1534del others(6): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459072 | |||||
chr22:39459072
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0005g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2+1524_-2+1534del others(11): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459072 | |||||
chr22:39459073
|
T | TTTTCTTT others(2): Show |
9 | a0001c0001t0001g0010a0001c0001t0001g0067a0001c0001t0001g0071others(6): Show | 11 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(9): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | |||||
chr22:39459073
|
T | TTTTCTTT others(7): Show |
1 | a0001c0001t0001g0034 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(14): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | |||||
chr22:39459073
|
T | TTTTCTTT others(12): Show |
1 | a0001c0001t0001g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(19): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | |||||
chr22:39459073
|
T | TTTTCTTT others(17): Show |
1 | a0001c0002t0002g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(24): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | |||||
chr22:39459078
|
T | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0064others(22): Show | 28 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2+1521T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459078 | ||||||
chr22:39459083
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-2+1526T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459083 | ||||||
chr22:39459123
|
G | C | 1 | a0001c0001t0019g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+1566G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459123 | ||||||
chr22:39459185
|
C | T | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240 | 3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+1628C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459185 | ||||||
chr22:39459489
|
G | A | 1 | a0003c0009t0003g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+1932G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459489 | ||||||
chr22:39459535
|
G | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-2+1978G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459535 | ||||||
chr22:39459570
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-2+2013C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459570 | ||||||
chr22:39459723
|
G | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-2+2166G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459723 | ||||||
chr22:39459878
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-2+2321C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459878 | ||||||
chr22:39460027
|
A | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(134): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-2+2470A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460027 | ||||||
chr22:39460278
|
G | T | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240 | 3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+2721G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460278 | ||||||
chr22:39460351
|
G | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-2+2794G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460351 | ||||||
chr22:39460496
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+2939T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460496 | ||||||
chr22:39460510
|
C | T | 8 | a0001c0001t0006g0031a0001c0001t0006g0214a0001c0001t0006g0215others(5): Show | 9 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+2953C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460510 | ||||||
chr22:39460650
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2+3093T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460650 | ||||||
chr22:39460976
|
A | T | 2 | a0001c0003t0002g0206a0001c0003t0002g0207 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-2+3419A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460976 | ||||||
chr22:39461042
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+3485C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461042 | ||||||
chr22:39461320
|
G | C | 1 | a0001c0001t0019g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+3763G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461320 | ||||||
chr22:39461413
|
G | A | 2 | a0001c0003t0002g0206a0001c0003t0002g0207 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-2+3856G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461413 | ||||||
chr22:39461635
|
T | C | 2 | a0001c0001t0011g0030a0001c0001t0027g0030 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+4078T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461635 | ||||||
chr22:39461721
|
C | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0064others(15): Show | 21 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+4164C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461721 | ||||||
chr22:39461885
|
T | C | 5 | a0001c0001t0003g0078a0001c0001t0010g0079a0001c0002t0002g0076others(2): Show | 5 | HG02280.hp1 HG02922.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+4328T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461885 | ||||||
chr22:39461904
|
C | CT | 6 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240others(3): Show | 6 | HG02129.hp1 HG02257.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+4359dupT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39461904 | |||||
chr22:39461904
|
CT | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0064others(18): Show | 24 | HG00639.hp1 HG01243.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2+4359delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39461904 | |||||
chr22:39461957
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+4400A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461957 | ||||||
chr22:39462012
|
C | T | 2 | a0001c0002t0002g0125a0001c0002t0005g0126 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-2+4455C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462012 | ||||||
chr22:39462048
|
C | T | 4 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240others(1): Show | 4 | HG02129.hp1 HG02257.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+4491C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462048 | ||||||
chr22:39462178
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-2+4621C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462178 | ||||||
chr22:39462191
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-2+4634A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462191 | ||||||
chr22:39462322
|
C | T | 12 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240others(9): Show | 13 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+4765C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462322 | ||||||
chr22:39462412
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-2+4855A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462412 | ||||||
chr22:39463047
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+5490G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463047 | ||||||
chr22:39463053
|
A | T | 8 | a0001c0001t0006g0031a0001c0001t0006g0214a0001c0001t0006g0215others(5): Show | 9 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+5496A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463053 | ||||||
chr22:39463164
|
C | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-2+5607C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463164 | ||||||
chr22:39463167
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-2+5610A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463167 | ||||||
chr22:39463231
|
C | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-2+5674C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463231 | ||||||
chr22:39463518
|
C | G | 18 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+5961C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463518 | ||||||
chr22:39463538
|
G | A | 18 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+5981G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463538 | ||||||
chr22:39463584
|
C | T | 1 | a0003c0009t0003g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+6027C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463584 | ||||||
chr22:39463757
|
A | T | 2 | a0001c0001t0003g0078a0001c0001t0010g0079 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2+6200A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463757 | ||||||
chr22:39463921
|
T | TA | 10 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0134others(7): Show | 10 | HG02165.hp2 HG02602.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+6373dupA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39463921 | |||||
chr22:39463921
|
TA | T | 18 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+6373delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39463921 | |||||
chr22:39464125
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-2+6568C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464125 | ||||||
chr22:39464194
|
G | C | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240 | 3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+6637G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464194 | ||||||
chr22:39464196
|
A | T | 3 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240 | 3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+6639A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464196 | ||||||
chr22:39464237
|
G | A | 1 | a0001c0002t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2+6680G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464237 | ||||||
chr22:39464237
|
G | T | 1 | a0001c0002t0018g0235 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2+6680G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464237 | ||||||
chr22:39464259
|
C | T | 1 | a0001c0001t0019g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+6702C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464259 | ||||||
chr22:39464260
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0242others(1): Show | 7 | HG02280.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+6703C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464260 | ||||||
chr22:39464409
|
C | A | 9 | a0001c0001t0006g0031a0001c0001t0006g0214a0001c0001t0006g0215others(6): Show | 10 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+6852C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464409 | ||||||
chr22:39464458
|
G | T | 1 | a0001c0001t0020g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2+6901G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464458 | ||||||
chr22:39464463
|
G | A | 18 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+6906G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464463 | ||||||
chr22:39464488
|
G | A | 1 | a0001c0001t0019g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+6931G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464488 | ||||||
chr22:39464584
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-2+7027A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464584 | ||||||
chr22:39464790
|
GC | G | 4 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0240others(1): Show | 4 | HG02129.hp1 HG02257.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+7236delC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39464790 | |||||
chr22:39464851
|
C | T | 1 | a0001c0001t0008g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2+7294C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464851 | ||||||
chr22:39464863
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-2+7306A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464863 | ||||||
chr22:39464902
|
C | T | 2 | a0001c0001t0011g0073a0001c0001t0011g0074 | 2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-2+7345C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464902 | ||||||
chr22:39465172
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0028g0203 | 2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-2+7615A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465172 | ||||||
chr22:39465404
|
C | G | 1 | a0001c0002t0002g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2+7847C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465404 | ||||||
chr22:39465515
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+7958C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465515 | ||||||
chr22:39465653
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2+8096A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465653 | ||||||
chr22:39465697
|
C | T | 13 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0071others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+8140C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465697 | ||||||
chr22:39465760
|
C | T | 2 | a0001c0003t0002g0206a0001c0003t0002g0207 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-2+8203C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465760 | ||||||
chr22:39465931
|
TA | T | 9 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0200others(6): Show | 9 | HG00639.hp1 HG01516.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+8391delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39465931 | |||||
chr22:39466033
|
G | T | 1 | a0001c0001t0006g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2+8476G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466033 | ||||||
chr22:39466062
|
G | T | 1 | a0001c0001t0019g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+8505G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466062 | ||||||
chr22:39466183
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-2+8626C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466183 | ||||||
chr22:39466200
|
C | T | 1 | a0001c0002t0005g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2+8643C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466200 | ||||||
chr22:39466336
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(197): Show | 237 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-2+8779G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466336 | ||||||
chr22:39466338
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(98): Show | 130 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-2+8781T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466338 | ||||||
chr22:39466384
|
A | G | 1 | a0001c0001t0005g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2+8827A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466384 | ||||||
chr22:39466468
|
G | A | 1 | a0001c0002t0002g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-2+8911G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466468 | ||||||
chr22:39466484
|
C | T | 10 | a0001c0001t0001g0064a0001c0001t0007g0083a0001c0001t0008g0208others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+8927C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466484 | ||||||
chr22:39466485
|
C | G | 9 | a0001c0001t0001g0244a0001c0001t0006g0217a0001c0001t0008g0174others(6): Show | 9 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+8928C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466485 | ||||||
chr22:39466558
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+9001C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466558 | ||||||
chr22:39466573
|
C | T | 1 | a0001c0001t0039g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2+9016C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466573 | ||||||
chr22:39466677
|
G | C | 1 | a0001c0001t0004g0240 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-2+9120G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466677 | ||||||
chr22:39466693
|
G | T | 1 | a0001c0001t0008g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2+9136G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466693 | ||||||
chr22:39466848
|
T | C | 1 | a0001c0002t0002g0057 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2+9291T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466848 | ||||||
chr22:39466997
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+9440T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466997 | ||||||
chr22:39467041
|
C | T | 4 | a0001c0001t0003g0014a0001c0001t0003g0088a0001c0001t0003g0105others(1): Show | 5 | HG00642.hp1 HG01255.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+9484C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467041 | ||||||
chr22:39467080
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2+9523A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467080 | ||||||
chr22:39467140
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-2+9583G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467140 | ||||||
chr22:39467304
|
G | T | 1 | a0001c0001t0004g0240 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-2+9747G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467304 | ||||||
chr22:39467321
|
G | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 124 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-2+9764G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467321 | ||||||
chr22:39467332
|
A | G | 1 | a0001c0002t0005g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2+9775A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467332 | ||||||
chr22:39467346
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+9789G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467346 | ||||||
chr22:39467366
|
G | A | 1 | a0001c0001t0032g0143 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-2+9809G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467366 | ||||||
chr22:39467435
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2+9878C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467435 | ||||||
chr22:39467493
|
A | G | 1 | a0001c0001t0001g0029 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-2+9936A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467493 | ||||||
chr22:39467519
|
GTGGGCAG others(6): Show |
G | 1 | a0001c0001t0006g0228 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-2+9965_-2+9977del others(13): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467519 | |||||
chr22:39467640
|
TTTTTC | T | 5 | a0001c0001t0001g0064a0001c0001t0011g0030a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+10099_-2+10103d others(7): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467640 | |||||
chr22:39467671
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2+10114G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467671 | ||||||
chr22:39467716
|
T | TGTTTCGT others(3): Show |
11 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(8): Show | 14 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2+10168_-2+10169i others(12): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467716 | |||||
chr22:39467722
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-2+10165G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467722 | ||||||
chr22:39467726
|
T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0082others(21): Show | 28 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2+10169T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467726 | ||||||
chr22:39467733
|
T | C | 1 | a0001c0002t0002g0057 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2+10176T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467733 | ||||||
chr22:39467739
|
T | C | 6 | a0001c0002t0002g0039a0001c0002t0002g0043a0001c0002t0002g0044others(3): Show | 6 | HG00597.hp1 HG00597.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+10182T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467739 | ||||||
chr22:39467771
|
G | A | 3 | a0001c0002t0002g0065a0001c0002t0002g0068a0001c0002t0002g0125 | 3 | HG01109.hp1 HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2+10214G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467771 | ||||||
chr22:39467809
|
C | CA | 30 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0082others(27): Show | 34 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+10272dupA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467809 | |||||
chr22:39467809
|
CA | C | 19 | a0001c0001t0001g0021a0001c0001t0001g0104a0001c0001t0001g0129others(16): Show | 21 | HG01496.hp1 HG01515.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+10272delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467809 | |||||
chr22:39467828
|
A | T | 1 | a0001c0001t0001g0037 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-2+10271A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467828 | ||||||
chr22:39467845
|
G | T | 1 | a0001c0001t0020g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2+10288G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467845 | ||||||
chr22:39467975
|
A | G | 3 | a0001c0001t0031g0171a0001c0004t0009g0008a0001c0004t0009g0172 | 5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+10418A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467975 | ||||||
chr22:39468124
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-2+10567C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468124 | ||||||
chr22:39468194
|
G | A | 2 | a0001c0002t0005g0209a0001c0005t0015g0011 | 3 | HG02559.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+10637G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468194 | ||||||
chr22:39468344
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+10787C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468344 | ||||||
chr22:39468513
|
A | T | 3 | a0001c0001t0005g0117a0001c0001t0019g0237a0001c0002t0016g0210 | 3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+10956A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468513 | ||||||
chr22:39468638
|
CAGGCCTG others(546): Show |
C | 3 | a0001c0001t0011g0030a0001c0001t0027g0030a0001c0002t0002g0057 | 3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+11084_-2+11636d others(2): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39468638 | |||||
chr22:39468766
|
C | T | 1 | a0003c0009t0003g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+11209C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468766 | ||||||
chr22:39469009
|
G | A | 1 | a0001c0001t0003g0027 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-2+11452G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469009 | ||||||
chr22:39469253
|
T | C | 2 | a0001c0001t0004g0220a0002c0006t0001g0148 | 2 | NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-2+11696T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469253 | ||||||
chr22:39469470
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 235 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-2+11913A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469470 | ||||||
chr22:39469505
|
C | T | 3 | a0001c0001t0005g0117a0001c0001t0019g0237a0001c0002t0016g0210 | 3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+11948C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469505 | ||||||
chr22:39469830
|
G | A | 1 | a0003c0009t0003g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+12273G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469830 | ||||||
chr22:39469919
|
G | A | 1 | a0001c0002t0005g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2+12362G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469919 | ||||||
chr22:39470050
|
G | T | 3 | a0001c0001t0005g0117a0001c0001t0019g0237a0001c0002t0016g0210 | 3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+12493G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470050 | ||||||
chr22:39470075
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(110): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-2+12518T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470075 | ||||||
chr22:39470161
|
C | T | 3 | a0001c0001t0005g0117a0001c0001t0019g0237a0001c0002t0016g0210 | 3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+12604C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470161 | ||||||
chr22:39470162
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0201 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-2+12605G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470162 | ||||||
chr22:39470170
|
C | T | 1 | a0001c0001t0032g0143 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-2+12613C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470170 | ||||||
chr22:39470171
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+12614G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470171 | ||||||
chr22:39470194
|
TC | T | 3 | a0001c0001t0005g0117a0001c0001t0019g0237a0001c0002t0016g0210 | 3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+12638delC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470194 | ||||||
chr22:39470324
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0004g0222 | 3 | HG02615.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-2+12767G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470324 | ||||||
chr22:39470378
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0160 | 3 | HG03704.hp1 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-2+12821A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470378 | ||||||
chr22:39470451
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+12894C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470451 | ||||||
chr22:39470466
|
G | A | 2 | a0001c0001t0011g0073a0001c0001t0011g0074 | 2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-2+12909G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470466 | ||||||
chr22:39470714
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+13157C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470714 | ||||||
chr22:39470789
|
G | A | 5 | a0001c0001t0001g0080a0001c0001t0001g0161a0001c0001t0001g0173others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+13232G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470789 | ||||||
chr22:39470933
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(108): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-2+13376T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470933 | ||||||
chr22:39471078
|
G | A | 2 | a0001c0002t0005g0209a0001c0005t0015g0011 | 3 | HG02559.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+13521G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471078 | ||||||
chr22:39471382
|
C | T | 2 | a0001c0001t0006g0217a0001c0001t0006g0219 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-2+13825C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471382 | ||||||
chr22:39471582
|
C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+14025C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471582 | ||||||
chr22:39471599
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-2+14042C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471599 | ||||||
chr22:39471654
|
C | T | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+14097C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471654 | ||||||
chr22:39471656
|
C | G | 88 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0082others(85): Show | 99 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.-2+14099C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471656 | ||||||
chr22:39471813
|
A | G | 1 | a0001c0002t0018g0235 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2+14256A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471813 | ||||||
chr22:39471964
|
G | C | 3 | a0001c0001t0003g0110a0001c0001t0008g0111a0001c0001t0008g0243 | 3 | HG02886.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-2+14407G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471964 | ||||||
chr22:39472104
|
G | C | 75 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0066others(72): Show | 82 | HG00140.hp2 HG00639.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.-2+14547G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472104 | ||||||
chr22:39472120
|
A | G | 10 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0036others(7): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+14563A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472120 | ||||||
chr22:39472155
|
C | T | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+14598C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472155 | ||||||
chr22:39472178
|
C | T | 1 | a0001c0002t0002g0076 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-2+14621C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472178 | ||||||
chr22:39472254
|
C | G | 1 | a0001c0001t0040g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-2+14697C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472254 | ||||||
chr22:39472296
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+14739T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472296 | ||||||
chr22:39472339
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2+14782G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472339 | ||||||
chr22:39472369
|
A | G | 1 | a0001c0002t0005g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-2+14812A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472369 | ||||||
chr22:39472428
|
A | G | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+14871A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472428 | ||||||
chr22:39472503
|
A | G | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-14844A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472503 | ||||||
chr22:39472684
|
G | A | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-14663G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472684 | ||||||
chr22:39472794
|
G | A | 3 | a0001c0001t0031g0171a0001c0004t0009g0008a0001c0004t0009g0172 | 5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-14553G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472794 | ||||||
chr22:39472862
|
T | C | 1 | a0001c0001t0028g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-1-14485T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472862 | ||||||
chr22:39472870
|
A | C | 1 | a0001c0001t0033g0190 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1-14477A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472870 | ||||||
chr22:39472886
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0029g0063 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-1-14461G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472886 | ||||||
chr22:39473204
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(178): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-1-14143C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473204 | ||||||
chr22:39473577
|
A | G | 3 | a0001c0001t0031g0171a0001c0004t0009g0008a0001c0004t0009g0172 | 5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-13770A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473577 | ||||||
chr22:39473578
|
T | G | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-13769T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473578 | ||||||
chr22:39473714
|
A | G | 55 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0066others(52): Show | 60 | HG00140.hp2 HG01109.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.-1-13633A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473714 | ||||||
chr22:39473774
|
C | T | 1 | a0001c0001t0004g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-1-13573C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473774 | ||||||
chr22:39473992
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(178): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-1-13355T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473992 | ||||||
chr22:39474294
|
G | T | 2 | a0001c0001t0005g0117a0001c0001t0019g0237 | 2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-13053G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474294 | ||||||
chr22:39474304
|
A | G | 1 | a0001c0001t0005g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1-13043A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474304 | ||||||
chr22:39474553
|
A | G | 2 | a0001c0001t0014g0084a0001c0001t0014g0086 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-12794A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474553 | ||||||
chr22:39474655
|
C | G | 3 | a0001c0001t0003g0110a0001c0001t0008g0111a0001c0001t0008g0243 | 3 | HG02886.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-12692C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474655 | ||||||
chr22:39474662
|
C | T | 1 | a0001c0002t0005g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1-12685C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474662 | ||||||
chr22:39474795
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1-12552G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474795 | ||||||
chr22:39474814
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 8 | HG00735.hp1 HG01255.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-12533G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474814 | ||||||
chr22:39474909
|
G | A | 1 | a0001c0001t0001g0019 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-1-12438G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474909 | ||||||
chr22:39474970
|
G | A | 1 | a0001c0002t0005g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-12377G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474970 | ||||||
chr22:39474982
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1-12365C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474982 | ||||||
chr22:39474998
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-1-12349C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474998 | ||||||
chr22:39475052
|
A | G | 3 | a0001c0001t0031g0171a0001c0004t0009g0008a0001c0004t0009g0172 | 5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-12295A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475052 | ||||||
chr22:39475074
|
C | T | 1 | a0001c0001t0007g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-1-12273C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475074 | ||||||
chr22:39475122
|
G | C | 3 | a0001c0001t0003g0110a0001c0001t0008g0111a0001c0001t0008g0243 | 3 | HG02886.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-12225G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475122 | ||||||
chr22:39475123
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-1-12224C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475123 | ||||||
chr22:39475128
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0161 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-1-12206_-1-12197d others(12): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0085others(1): Show | 4 | HG02809.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-12212_-1-12197d others(18): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0173 | 6 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-12213_-1-12197d others(19): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-1-12217_-1-12197d others(23): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0038g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(26): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(27): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(34): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0245 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(35): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
CT | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0061others(39): Show | 51 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1-12197delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
CTT | C | 9 | a0001c0001t0001g0064a0001c0001t0001g0089a0001c0001t0001g0164others(6): Show | 11 | HG01081.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-12198_-1-12197d others(4): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
CTTT | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 107 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-1-12199_-1-12197d others(5): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475128
|
CTTTT | C | 6 | a0001c0001t0005g0117a0001c0001t0011g0073a0001c0001t0011g0074others(3): Show | 6 | HG00639.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-12200_-1-12197d others(6): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | |||||
chr22:39475490
|
G | A | 1 | a0001c0002t0005g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-11857G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475490 | ||||||
chr22:39475561
|
C | T | 1 | a0001c0001t0032g0143 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-1-11786C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475561 | ||||||
chr22:39475574
|
T | G | 1 | a0001c0001t0006g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1-11773T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475574 | ||||||
chr22:39475616
|
G | A | 1 | a0001c0002t0005g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-11731G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475616 | ||||||
chr22:39475723
|
A | G | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0168others(8): Show | 11 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-11624A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475723 | ||||||
chr22:39475784
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-1-11563C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475784 | ||||||
chr22:39475938
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0090others(8): Show | 14 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-11409C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475938 | ||||||
chr22:39476009
|
C | T | 1 | a0001c0001t0008g0243 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-1-11338C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476009 | ||||||
chr22:39476068
|
A | G | 69 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0056others(66): Show | 74 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1-11279A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476068 | ||||||
chr22:39476122
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(175): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-1-11225A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476122 | ||||||
chr22:39476174
|
A | C | 2 | a0001c0001t0014g0084a0001c0001t0014g0086 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-11173A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476174 | ||||||
chr22:39476211
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-1-11136G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476211 | ||||||
chr22:39476302
|
A | G | 9 | a0001c0001t0003g0110a0001c0001t0005g0117a0001c0001t0008g0111others(6): Show | 9 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-11045A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476302 | ||||||
chr22:39476411
|
G | A | 3 | a0001c0001t0011g0030a0001c0001t0027g0030a0001c0002t0002g0057 | 3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-10936G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476411 | ||||||
chr22:39476649
|
G | A | 6 | a0001c0001t0002g0047a0001c0001t0007g0006a0001c0001t0007g0048others(3): Show | 8 | HG01175.hp1 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-10698G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476649 | ||||||
chr22:39476674
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1-10673C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476674 | ||||||
chr22:39476695
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(61): Show | 86 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1-10652C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476695 | ||||||
chr22:39476702
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(171): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-1-10645G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476702 | ||||||
chr22:39476800
|
C | T | 10 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0036others(7): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-10547C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476800 | ||||||
chr22:39476851
|
C | CACTTTGT others(13): Show |
1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-10495_-1-10476d others(22): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39476851 | |||||
chr22:39476939
|
T | C | 1 | a0001c0001t0004g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-1-10408T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476939 | ||||||
chr22:39477053
|
A | G | 4 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0014g0084others(1): Show | 4 | HG00639.hp1 HG01934.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-10294A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477053 | ||||||
chr22:39477318
|
C | T | 4 | a0001c0001t0003g0110a0001c0001t0008g0111a0001c0001t0008g0208others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-10029C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477318 | ||||||
chr22:39477465
|
A | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(187): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-1-9882A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477465 | ||||||
chr22:39477552
|
G | GA | 7 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0003g0165others(4): Show | 7 | HG00639.hp1 HG01361.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-9781dupA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39477552 | |||||
chr22:39477552
|
GA | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(84): Show | 116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-1-9781delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39477552 | |||||
chr22:39477567
|
C | A | 2 | a0001c0001t0006g0218a0001c0001t0022g0216 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-9780C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477567 | ||||||
chr22:39477624
|
C | T | 4 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0014g0084others(1): Show | 4 | HG00639.hp1 HG01934.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-9723C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477624 | ||||||
chr22:39477801
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0066others(7): Show | 13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-9546C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477801 | ||||||
chr22:39477864
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-9483C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477864 | ||||||
chr22:39477910
|
G | A | 3 | a0001c0001t0011g0030a0001c0001t0027g0030a0001c0002t0002g0057 | 3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-9437G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477910 | ||||||
chr22:39477914
|
C | A | 1 | a0001c0002t0002g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-1-9433C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477914 | ||||||
chr22:39477924
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0189a0001c0001t0004g0225 | 4 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-9423G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477924 | ||||||
chr22:39477932
|
G | A | 26 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0122others(23): Show | 34 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1-9415G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477932 | ||||||
chr22:39478151
|
G | A | 2 | a0001c0001t0004g0227a0001c0002t0005g0126 | 2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1-9196G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478151 | ||||||
chr22:39478153
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-1-9194G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478153 | ||||||
chr22:39478309
|
A | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-1-9038A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478309 | ||||||
chr22:39478315
|
A | G | 1 | a0001c0002t0002g0076 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-1-9032A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478315 | ||||||
chr22:39478361
|
A | G | 5 | a0001c0001t0003g0110a0001c0001t0008g0111a0001c0001t0008g0208others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-8986A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478361 | ||||||
chr22:39478566
|
G | C | 8 | a0001c0001t0001g0064a0001c0001t0001g0104a0001c0001t0001g0244others(5): Show | 8 | HG02965.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-8781G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478566 | ||||||
chr22:39478785
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0017others(133): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-1-8562A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478785 | ||||||
chr22:39478832
|
C | T | 1 | a0001c0001t0004g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-1-8515C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478832 | ||||||
chr22:39478917
|
C | T | 1 | a0001c0001t0004g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-1-8430C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478917 | ||||||
chr22:39479135
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG00738.hp1 HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-1-8212C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479135 | ||||||
chr22:39479195
|
GCCGAGTG others(10): Show |
G | 2 | a0001c0001t0001g0137a0001c0001t0003g0167 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-1-8149_-1-8133del others(17): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39479195 | |||||
chr22:39479213
|
C | T | 1 | a0001c0002t0005g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-8134C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479213 | ||||||
chr22:39479310
|
G | T | 1 | a0001c0005t0015g0011 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-8037G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479310 | ||||||
chr22:39479442
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1-7905T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479442 | ||||||
chr22:39479459
|
G | A | 1 | a0001c0001t0004g0230 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-1-7888G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479459 | ||||||
chr22:39479532
|
C | T | 1 | a0001c0002t0002g0045 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-1-7815C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479532 | ||||||
chr22:39479590
|
G | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(169): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-1-7757G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479590 | ||||||
chr22:39479620
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0038g0051 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-1-7727C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479620 | ||||||
chr22:39479662
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1-7685T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479662 | ||||||
chr22:39479785
|
C | G | 1 | a0001c0001t0030g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-1-7562C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479785 | ||||||
chr22:39479790
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1-7557C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479790 | ||||||
chr22:39479835
|
C | T | 1 | a0001c0001t0008g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-7512C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479835 | ||||||
chr22:39479848
|
T | C | 1 | a0001c0005t0015g0011 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-7499T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479848 | ||||||
chr22:39479856
|
C | T | 1 | a0001c0002t0016g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-7491C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479856 | ||||||
chr22:39479910
|
C | T | 3 | a0001c0001t0031g0171a0001c0004t0009g0008a0001c0004t0009g0172 | 5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-7437C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479910 | ||||||
chr22:39479961
|
T | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-1-7386T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479961 | ||||||
chr22:39480099
|
C | T | 3 | a0001c0001t0031g0171a0001c0004t0009g0008a0001c0004t0009g0172 | 5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-7248C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480099 | ||||||
chr22:39480316
|
C | T | 2 | a0001c0002t0002g0112a0001c0002t0002g0116 | 2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-1-7031C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480316 | ||||||
chr22:39480336
|
C | T | 10 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0036others(7): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-7011C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480336 | ||||||
chr22:39480361
|
C | A | 1 | a0001c0002t0005g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-6986C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480361 | ||||||
chr22:39480366
|
G | A | 2 | a0001c0001t0014g0084a0001c0001t0014g0086 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-6981G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480366 | ||||||
chr22:39480579
|
C | T | 2 | a0001c0001t0008g0208a0003c0009t0003g0075 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-1-6768C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480579 | ||||||
chr22:39480768
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0005g0117a0001c0001t0019g0237 | 3 | HG01884.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-6579G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480768 | ||||||
chr22:39480833
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0004g0032 | 4 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6514A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480833 | ||||||
chr22:39481082
|
G | T | 31 | a0001c0001t0001g0049a0001c0001t0001g0080a0001c0001t0001g0082others(28): Show | 34 | HG01167.hp1 HG01175.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1-6265G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481082 | ||||||
chr22:39481336
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 10 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-6011C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481336 | ||||||
chr22:39481337
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0164a0001c0001t0001g0173others(15): Show | 22 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1-6010G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481337 | ||||||
chr22:39481391
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 11 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-5956G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481391 | ||||||
chr22:39481479
|
C | T | 1 | a0001c0002t0005g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-1-5868C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481479 | ||||||
chr22:39481551
|
G | T | 8 | a0001c0002t0002g0076a0001c0002t0002g0077a0001c0002t0002g0112others(5): Show | 8 | HG01167.hp1 HG03490.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5796G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481551 | ||||||
chr22:39481642
|
G | A | 6 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0050others(3): Show | 8 | HG01175.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-5705G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481642 | ||||||
chr22:39481808
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-5539C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481808 | ||||||
chr22:39481809
|
T | C | 12 | a0001c0001t0005g0117a0001c0001t0019g0237a0001c0002t0005g0015others(9): Show | 14 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5538T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481809 | ||||||
chr22:39481816
|
G | A | 1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-5531G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481816 | ||||||
chr22:39481844
|
G | A | 7 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0050others(4): Show | 9 | HG00609.hp2 HG01175.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-5503G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481844 | ||||||
chr22:39482147
|
A | AT | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(90): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-1-5180dupT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39482147 | |||||
chr22:39482147
|
AT | A | 11 | a0001c0001t0008g0111a0001c0001t0008g0208a0001c0001t0008g0243others(8): Show | 11 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-5180delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39482147 | |||||
chr22:39482147
|
ATTTTTT | A | 24 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0027others(21): Show | 28 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-5185_-1-5180del others(6): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39482147 | |||||
chr22:39482559
|
C | G | 1 | a0003c0009t0003g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-1-4788C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482559 | ||||||
chr22:39482692
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-1-4655G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482692 | ||||||
chr22:39482936
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-4411G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482936 | ||||||
chr22:39482948
|
C | T | 1 | a0001c0002t0018g0235 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-1-4399C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482948 | ||||||
chr22:39482951
|
G | C | 1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-4396G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482951 | ||||||
chr22:39482993
|
T | C | 62 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0049others(59): Show | 71 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-1-4354T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482993 | ||||||
chr22:39483035
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-1-4312C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483035 | ||||||
chr22:39483057
|
T | C | 1 | a0001c0001t0008g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-4290T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483057 | ||||||
chr22:39483297
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG00741.hp1 HG01361.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-4050C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483297 | ||||||
chr22:39483415
|
G | A | 3 | a0001c0001t0008g0111a0001c0001t0008g0208a0001c0001t0008g0243 | 3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-3932G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483415 | ||||||
chr22:39483439
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0066others(4): Show | 10 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-3908C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483439 | ||||||
chr22:39483467
|
A | G | 2 | a0001c0002t0002g0077a0001c0002t0002g0128 | 2 | NA18963.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-1-3880A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483467 | ||||||
chr22:39483501
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-1-3846T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483501 | ||||||
chr22:39483502
|
TA | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0049others(97): Show | 114 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.-1-3834delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39483502 | |||||
chr22:39483626
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-3721C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483626 | ||||||
chr22:39483644
|
C | G | 3 | a0001c0001t0008g0111a0001c0001t0008g0208a0001c0001t0008g0243 | 3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-3703C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483644 | ||||||
chr22:39483674
|
A | T | 106 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0049others(103): Show | 122 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.-1-3673A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483674 | ||||||
chr22:39483946
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-1-3401C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483946 | ||||||
chr22:39483960
|
G | A | 2 | a0001c0001t0006g0218a0001c0001t0022g0216 | 2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-3387G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483960 | ||||||
chr22:39484021
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-1-3326C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484021 | ||||||
chr22:39484148
|
A | T | 1 | a0001c0001t0008g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-3199A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484148 | ||||||
chr22:39484163
|
A | G | 5 | a0001c0001t0011g0030a0001c0001t0011g0073a0001c0001t0011g0074others(2): Show | 5 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-3184A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484163 | ||||||
chr22:39484361
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-1-2986T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484361 | ||||||
chr22:39484365
|
T | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0188 | 2 | HG02080.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-1-2982T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484365 | ||||||
chr22:39484438
|
T | A | 1 | a0001c0001t0004g0220 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-1-2909T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484438 | ||||||
chr22:39484536
|
C | G | 3 | a0001c0001t0011g0030a0001c0001t0027g0030a0001c0002t0002g0057 | 3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-2811C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484536 | ||||||
chr22:39484995
|
C | T | 118 | a0001c0001t0001g0009a0001c0001t0001g0049a0001c0001t0001g0071others(115): Show | 137 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.-1-2352C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484995 | ||||||
chr22:39485135
|
T | G | 28 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 33 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1-2212T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485135 | ||||||
chr22:39485256
|
A | G | 2 | a0001c0004t0009g0008a0001c0004t0009g0172 | 4 | NA18964.hp2 NA19007.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-2091A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485256 | ||||||
chr22:39485285
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-1-2062G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485285 | ||||||
chr22:39485565
|
C | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1782C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485565 | ||||||
chr22:39485566
|
G | A | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1781G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485566 | ||||||
chr22:39485587
|
T | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1760T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485587 | ||||||
chr22:39485588
|
C | G | 5 | a0001c0001t0011g0030a0001c0001t0011g0073a0001c0001t0011g0074others(2): Show | 5 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1759C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485588 | ||||||
chr22:39485588
|
C | T | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1759C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485588 | ||||||
chr22:39485590
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A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1757A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485590 | ||||||
chr22:39485592
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A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1755A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485592 | ||||||
chr22:39485593
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C | T | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1754C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485593 | ||||||
chr22:39485594
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C | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1753C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485594 | ||||||
chr22:39485598
|
C | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1749C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485598 | ||||||
chr22:39485600
|
A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1747A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485600 | ||||||
chr22:39485607
|
A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1740A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485607 | ||||||
chr22:39485611
|
C | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1736C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485611 | ||||||
chr22:39485612
|
GAAACCCC others(23): Show |
G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1734_-1-1705del others(30): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485612 | ||||||
chr22:39485643
|
T | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1704T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485643 | ||||||
chr22:39485644
|
A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1703A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485644 | ||||||
chr22:39485646
|
C | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1701C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485646 | ||||||
chr22:39485651
|
T | A | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1696T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485651 | ||||||
chr22:39485654
|
G | GGGAATGA others(3): Show |
1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1692_-1-1691ins others(10): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39485654 | |||||
chr22:39485744
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1-1603G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485744 | ||||||
chr22:39485816
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C | A | 1 | a0001c0001t0008g0111 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1-1531C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485816 | ||||||
chr22:39485833
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G | A | 1 | a0001c0001t0001g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1-1514G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485833 | ||||||
chr22:39485881
|
T | G | 3 | a0001c0001t0008g0111a0001c0001t0008g0208a0001c0001t0008g0243 | 3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-1466T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485881 | ||||||
chr22:39485895
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-1-1452G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485895 | ||||||
chr22:39485951
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-1-1396C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485951 | ||||||
chr22:39485953
|
C | G | 1 | a0001c0003t0002g0169 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-1-1394C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485953 | ||||||
chr22:39486007
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G | A | 1 | a0001c0001t0012g0229 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1-1340G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486007 | ||||||
chr22:39486144
|
AT | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-1-1184delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39486144 | |||||
chr22:39486144
|
ATT | A | 65 | a0001c0001t0001g0091a0001c0001t0001g0149a0001c0001t0001g0151others(62): Show | 77 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.-1-1185_-1-1184del others(2): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39486144 | |||||
chr22:39486163
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T | A | 1 | a0001c0001t0002g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-1184T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486163 | ||||||
chr22:39486179
|
C | G | 2 | a0001c0001t0014g0084a0001c0001t0014g0086 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-1168C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486179 | ||||||
chr22:39486554
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1-793G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486554 | ||||||
chr22:39486582
|
C | T | 1 | a0001c0001t0029g0063 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-765C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486582 | ||||||
chr22:39486781
|
G | A | 1 | a0001c0001t0029g0063 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-566G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486781 | ||||||
chr22:39486792
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-555C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486792 | ||||||
chr22:39486811
|
C | A | 6 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0050others(3): Show | 8 | HG01175.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-536C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486811 | ||||||
chr22:39486949
|
A | T | 1 | a0001c0001t0003g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-1-398A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486949 | ||||||
chr22:39487053
|
C | T | 3 | a0001c0002t0002g0007a0001c0002t0002g0035a0001c0002t0002g0162 | 5 | HG00597.hp2 HG00609.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-294C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39487053 | ||||||
chr22:39487246
|
AC | A | 3 | a0001c0001t0008g0111a0001c0001t0008g0208a0001c0001t0008g0243 | 3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-100delC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39487246 | ||||||
chr22:39487339
|
T | C | 53 | a0001c0001t0005g0117a0001c0001t0012g0226a0001c0001t0012g0229others(50): Show | 60 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.-1-8T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39487339 |